text: SARS-CoV-2/Human/USA/CA-CDC-VSX-A063930/2023

text: CDC-OAMD

text: live

text: SARS-CoV-2: clinical or host-associated

text: Helix

text: PrimeStore MTM - Nasal Swab

text: PrimeStore MTM - Nasal Swab

text: N

text: S

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: USA: California

text: Homo sapiens

text: Asian

text: male

text: PrimeStore MTM - Nasal Swab

text: baseline surveillance (random sampling)


status: PUBLIC

text: SARS-CoV-2/Human/USA/CA-CDC-VSX-A063917/2023

characteristic: External Id

text: CDC-OAMD

characteristic: INSDC center name

characteristic: INSDC first public

characteristic: INSDC last update

characteristic: INSDC secondary accession

text: live

characteristic: INSDC status

tag: attribute

characteristic: Isolate

text: SARS-CoV-2: clinical or host-associated

characteristic: NCBI submission model

characteristic: NCBI submission package

characteristic: SRA accession

text: Helix

text: PrimeStore MTM - Nasal Swab

text: PrimeStore MTM - Nasal Swab

text: N

text: S

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: USA: California

text: Homo sapiens

characteristic: host

text: Black

text: female

text: PrimeStore MTM - Nasal Swab

characteristic: lineage/clade name

text: Severe acute respiratory syndrome coronavirus 2

characteristic: organism

text: baseline surveillance (random sampling)

text: CDC Sars CoV2 Sequencing Baseline Constellation

characteristic: title


text: SARS-CoV-2/Human/USA/CA-CDC-VSX-A063905/2023

text: CDC-OAMD

text: live

text: SARS-CoV-2: clinical or host-associated

text: Helix

text: PrimeStore MTM - Nasal Swab

text: PrimeStore MTM - Nasal Swab

text: N

text: S

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: USA: California

text: Homo sapiens

text: Asian

text: female

text: PrimeStore MTM - Nasal Swab

text: baseline surveillance (random sampling)


text: SARS-CoV-2/Human/USA/CA-CDC-VSX-A063886/2023

text: CDC-OAMD

text: live

text: SARS-CoV-2: clinical or host-associated

text: Helix

text: PrimeStore MTM - Nasal Swab

text: PrimeStore MTM - Nasal Swab

text: N

text: S

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: USA: California

text: Homo sapiens

text: Other/Not Reported

text: female

text: PrimeStore MTM - Nasal Swab

text: baseline surveillance (random sampling)


text: SARS-CoV-2/Human/USA/CA-CDC-VSX-A063883/2023

text: CDC-OAMD

text: live

text: SARS-CoV-2: clinical or host-associated

text: Helix

text: PrimeStore MTM - Nasal Swab

text: PrimeStore MTM - Nasal Swab

text: N

text: S

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: USA: California

text: Homo sapiens

text: Other/Not Reported

text: female

text: PrimeStore MTM - Nasal Swab

text: baseline surveillance (random sampling)


text: SARS-CoV-2/Human/USA/CA-CDC-VSX-A063872/2023

text: CDC-OAMD

text: live

text: SARS-CoV-2: clinical or host-associated

text: Helix

text: PrimeStore MTM - Nasal Swab

text: PrimeStore MTM - Nasal Swab

text: N

text: S

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: USA: California

text: Homo sapiens

text: Other/Not Reported

text: female

text: PrimeStore MTM - Nasal Swab

text: baseline surveillance (random sampling)


text: SARS-CoV-2/Human/USA/CA-CDC-VSX-A063866/2023

text: CDC-OAMD

text: live

text: SARS-CoV-2: clinical or host-associated

text: Helix

text: PrimeStore MTM - Nasal Swab

text: PrimeStore MTM - Nasal Swab

text: N

text: S

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: USA: California

text: Homo sapiens

text: White

text: male

text: PrimeStore MTM - Nasal Swab

text: baseline surveillance (random sampling)


text: SARS-CoV-2/Human/USA/CA-CDC-VSX-A063854/2023

text: CDC-OAMD

text: live

text: SARS-CoV-2: clinical or host-associated

text: Helix

text: PrimeStore MTM - Nasal Swab

text: PrimeStore MTM - Nasal Swab

text: N

text: S

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: USA: California

text: Homo sapiens

text: Other/Not Reported

text: female

text: PrimeStore MTM - Nasal Swab

text: baseline surveillance (random sampling)


text: SARS-CoV-2/Human/USA/CA-CDC-VSX-A063848/2023

text: CDC-OAMD

text: live

text: SARS-CoV-2: clinical or host-associated

text: Helix

text: PrimeStore MTM - Nasal Swab

text: PrimeStore MTM - Nasal Swab

text: N

text: S

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: USA: California

text: Homo sapiens

text: Asian

text: female

text: PrimeStore MTM - Nasal Swab

text: baseline surveillance (random sampling)


text: SARS-CoV-2/Human/USA/CA-CDC-VSX-A063846/2023

text: CDC-OAMD

text: live

text: SARS-CoV-2: clinical or host-associated

text: Helix

text: PrimeStore MTM - Nasal Swab

text: PrimeStore MTM - Nasal Swab

text: N

text: S

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: USA: California

text: Homo sapiens

text: Asian

text: female

text: PrimeStore MTM - Nasal Swab

text: baseline surveillance (random sampling)


text: SARS-CoV-2/Human/USA/CA-CDC-VSX-A063829/2023

text: CDC-OAMD

text: live

text: SARS-CoV-2: clinical or host-associated

text: Helix

text: PrimeStore MTM - Nasal Swab

text: PrimeStore MTM - Nasal Swab

text: N

text: S

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: USA: California

text: Homo sapiens

text: Other/Not Reported

text: male

text: PrimeStore MTM - Nasal Swab

text: baseline surveillance (random sampling)


text: SARS-CoV-2/Human/USA/CA-CDC-VSX-A063823/2023

text: CDC-OAMD

text: live

text: SARS-CoV-2: clinical or host-associated

text: Helix

text: PrimeStore MTM - Nasal Swab

text: PrimeStore MTM - Nasal Swab

text: N

text: S

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: USA: California

text: Homo sapiens

text: White

text: female

text: PrimeStore MTM - Nasal Swab

text: baseline surveillance (random sampling)


text: SARS-CoV-2/Human/USA/CA-CDC-VSX-A063817/2023

text: CDC-OAMD

text: live

text: SARS-CoV-2: clinical or host-associated

text: Helix

text: PrimeStore MTM - Nasal Swab

text: PrimeStore MTM - Nasal Swab

text: N

text: S

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: USA: California

text: Homo sapiens

text: Asian

text: female

text: PrimeStore MTM - Nasal Swab

text: baseline surveillance (random sampling)


text: SARS-CoV-2/Human/USA/CA-CDC-VSX-A063813/2023

text: CDC-OAMD

text: live

text: SARS-CoV-2: clinical or host-associated

text: Helix

text: PrimeStore MTM - Nasal Swab

text: PrimeStore MTM - Nasal Swab

text: N

text: S

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: USA: California

text: Homo sapiens

text: Asian

text: female

text: PrimeStore MTM - Nasal Swab

text: baseline surveillance (random sampling)


text: SARS-CoV-2/Human/USA/CA-CDC-VSX-A063803/2023

text: CDC-OAMD

text: live

text: SARS-CoV-2: clinical or host-associated

text: Helix

text: PrimeStore MTM - Nasal Swab

text: PrimeStore MTM - Nasal Swab

text: N

text: S

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: USA: California

text: Homo sapiens

text: White

text: female

text: PrimeStore MTM - Nasal Swab

text: baseline surveillance (random sampling)


text: SARS-CoV-2/Human/USA/CA-CDC-VSX-A063776/2023

text: CDC-OAMD

text: live

text: SARS-CoV-2: clinical or host-associated

text: Helix

text: PrimeStore MTM - Nasal Swab

text: PrimeStore MTM - Nasal Swab

text: N

text: S

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: USA: California

text: Homo sapiens

text: Other/Not Reported

text: female

text: PrimeStore MTM - Nasal Swab

text: baseline surveillance (random sampling)


text: SARS-CoV-2/Human/USA/CA-CDC-VSX-A063774/2023

text: CDC-OAMD

text: live

text: SARS-CoV-2: clinical or host-associated

text: Helix

text: PrimeStore MTM - Nasal Swab

text: PrimeStore MTM - Nasal Swab

text: N

text: S

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: USA: California

text: Homo sapiens

text: Asian

text: male

text: PrimeStore MTM - Nasal Swab

text: baseline surveillance (random sampling)


text: SARS-CoV-2/Human/USA/CA-CDC-VSX-A063766/2023

text: CDC-OAMD

text: live

text: SARS-CoV-2: clinical or host-associated

text: Helix

text: PrimeStore MTM - Nasal Swab

text: PrimeStore MTM - Nasal Swab

text: N

text: S

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: USA: California

text: Homo sapiens

text: Asian

text: female

text: PrimeStore MTM - Nasal Swab

text: Severe acute respiratory syndrome coronavirus 2

text: baseline surveillance (random sampling)


text: SARS-CoV-2/Human/USA/CA-CDC-VSX-A063760/2023

text: CDC-OAMD

text: live

text: SARS-CoV-2: clinical or host-associated

text: Helix

text: PrimeStore MTM - Nasal Swab

text: PrimeStore MTM - Nasal Swab

text: N

text: S

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: USA: California

text: Homo sapiens

text: Other/Not Reported

text: male

text: PrimeStore MTM - Nasal Swab

text: baseline surveillance (random sampling)

text: CDC Sars CoV2 Sequencing Baseline Constellation


text: SARS-CoV-2/Human/USA/CA-CDC-VSX-A063753/2023

text: CDC-OAMD

text: live

text: SARS-CoV-2: clinical or host-associated

text: Helix

text: PrimeStore MTM - Nasal Swab

text: PrimeStore MTM - Nasal Swab

text: N

text: S

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: USA: California

text: Homo sapiens

text: Asian

text: female

text: PrimeStore MTM - Nasal Swab

text: baseline surveillance (random sampling)


text: SARS-CoV-2/Human/USA/CA-CDC-VSX-A063750/2023

text: CDC-OAMD

text: live

text: SARS-CoV-2: clinical or host-associated

text: Helix

text: PrimeStore MTM - Nasal Swab

text: PrimeStore MTM - Nasal Swab

text: N

text: S

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: USA: California

text: Homo sapiens

text: Other/Not Reported

text: female

text: PrimeStore MTM - Nasal Swab

text: baseline surveillance (random sampling)


text: SARS-CoV-2/Human/USA/CA-CDC-VSX-A063744/2023

text: CDC-OAMD

text: live

text: SARS-CoV-2: clinical or host-associated

text: Helix

text: PrimeStore MTM - Nasal Swab

text: PrimeStore MTM - Nasal Swab

text: N

text: S

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: USA: California

text: Homo sapiens

text: Other/Not Reported

text: male

text: PrimeStore MTM - Nasal Swab

text: baseline surveillance (random sampling)


text: SARS-CoV-2/Human/USA/CA-CDC-VSX-A063741/2023

text: CDC-OAMD

text: live

text: SARS-CoV-2: clinical or host-associated

text: Helix

text: PrimeStore MTM - Nasal Swab

text: PrimeStore MTM - Nasal Swab

text: N

text: S

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: USA: California

text: Homo sapiens

text: Other/Not Reported

text: female

text: PrimeStore MTM - Nasal Swab

text: baseline surveillance (random sampling)


text: SARS-CoV-2/Human/USA/AZ-CDC-VSX-A065865/2023

text: CDC-OAMD

text: live

text: SARS-CoV-2: clinical or host-associated

text: Helix

text: PrimeStore MTM - Nasal Swab

text: PrimeStore MTM - Nasal Swab

text: N

text: S

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: USA: Arizona

text: Homo sapiens

text: White

text: female

text: PrimeStore MTM - Nasal Swab

text: baseline surveillance (random sampling)


text: SARS-CoV-2/Human/USA/AZ-CDC-VSX-A065845/2023

text: CDC-OAMD

text: live

text: SARS-CoV-2: clinical or host-associated

text: Helix

text: PrimeStore MTM - Nasal Swab

text: PrimeStore MTM - Nasal Swab

text: N

text: S

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: USA: Arizona

text: Homo sapiens

text: Other/Not Reported

text: female

text: PrimeStore MTM - Nasal Swab

text: baseline surveillance (random sampling)


text: SARS-CoV-2/Human/USA/AZ-CDC-VSX-A065803/2023

text: CDC-OAMD

text: live

text: SARS-CoV-2: clinical or host-associated

text: Helix

text: PrimeStore MTM - Nasal Swab

text: PrimeStore MTM - Nasal Swab

text: N

text: S

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: USA: Arizona

text: Homo sapiens

text: Other/Not Reported

text: female

text: PrimeStore MTM - Nasal Swab

text: baseline surveillance (random sampling)


text: SARS-CoV-2/Human/USA/AZ-CDC-VSX-A065795/2023

text: CDC-OAMD

text: live

text: SARS-CoV-2: clinical or host-associated

text: Helix

text: PrimeStore MTM - Nasal Swab

text: PrimeStore MTM - Nasal Swab

text: N

text: S

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: USA: Arizona

text: Homo sapiens

text: White

text: female

text: PrimeStore MTM - Nasal Swab

text: baseline surveillance (random sampling)


text: SARS-CoV-2/Human/USA/AZ-CDC-VSX-A065743/2023

text: CDC-OAMD

text: live

text: SARS-CoV-2: clinical or host-associated

text: Helix

text: PrimeStore MTM - Nasal Swab

text: PrimeStore MTM - Nasal Swab

text: N

text: S

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: USA: Arizona

text: Homo sapiens

text: American Indian/Alaskan Native

text: female

text: PrimeStore MTM - Nasal Swab

text: baseline surveillance (random sampling)


text: SARS-CoV-2/Human/USA/AZ-CDC-VSX-A065726/2023

text: CDC-OAMD

text: live

text: SARS-CoV-2: clinical or host-associated

text: Helix

text: PrimeStore MTM - Nasal Swab

text: PrimeStore MTM - Nasal Swab

text: N

text: S

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: USA: Arizona

text: Homo sapiens

text: White

text: male

text: PrimeStore MTM - Nasal Swab

text: baseline surveillance (random sampling)


text: SARS-CoV-2/Human/USA/AZ-CDC-VSX-A063914/2023

text: CDC-OAMD

text: live

text: SARS-CoV-2: clinical or host-associated

text: Helix

text: PrimeStore MTM - Nasal Swab

text: PrimeStore MTM - Nasal Swab

text: N

text: S

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: USA: Arizona

text: Homo sapiens

text: White

text: female

text: PrimeStore MTM - Nasal Swab

text: baseline surveillance (random sampling)


text: SARS-CoV-2/Human/USA/AZ-CDC-VSX-A063877/2023

text: CDC-OAMD

text: live

text: SARS-CoV-2: clinical or host-associated

text: Helix

text: PrimeStore MTM - Nasal Swab

text: PrimeStore MTM - Nasal Swab

text: N

text: S

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: USA: Arizona

text: Homo sapiens

text: White

text: female

text: PrimeStore MTM - Nasal Swab

text: baseline surveillance (random sampling)


text: SARS-CoV-2/Human/USA/AZ-CDC-VSX-A063775/2023

text: CDC-OAMD

text: live

text: SARS-CoV-2: clinical or host-associated

text: Helix

text: PrimeStore MTM - Nasal Swab

text: PrimeStore MTM - Nasal Swab

text: N

text: S

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: USA: Arizona

text: Homo sapiens

text: White

text: female

text: PrimeStore MTM - Nasal Swab

text: baseline surveillance (random sampling)


text: SARS-CoV-2/Human/USA/AL-CDC-VSX-A063882/2023

text: CDC-OAMD

text: live

text: SARS-CoV-2: clinical or host-associated

text: Helix

text: PrimeStore MTM - Nasal Swab

text: PrimeStore MTM - Nasal Swab

text: N

text: S

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: USA: Alabama

text: Homo sapiens

text: Black

text: female

text: PrimeStore MTM - Nasal Swab

text: baseline surveillance (random sampling)


text: SARS-CoV-2/Human/USA/AL-CDC-VSX-A063879/2023

text: CDC-OAMD

text: live

text: SARS-CoV-2: clinical or host-associated

text: Helix

text: PrimeStore MTM - Nasal Swab

text: PrimeStore MTM - Nasal Swab

text: N

text: S

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: USA: Alabama

text: Homo sapiens

text: White

text: male

text: PrimeStore MTM - Nasal Swab

text: Severe acute respiratory syndrome coronavirus 2

text: baseline surveillance (random sampling)


text: SARS-CoV-2/Human/USA/AL-CDC-VSX-A063799/2023

text: CDC-OAMD

text: live

text: SARS-CoV-2: clinical or host-associated

text: Helix

text: PrimeStore MTM - Nasal Swab

text: PrimeStore MTM - Nasal Swab

text: N

text: S

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: Helix COVID-19 and Flu Test

text: USA: Alabama

text: Homo sapiens

text: American Indian/Alaskan Native

text: female

text: PrimeStore MTM - Nasal Swab

text: baseline surveillance (random sampling)

text: CDC Sars CoV2 Sequencing Baseline Constellation


text: Shanghai Academy of Agricultural Sciences

text: live

text: Metagenome or environmental

text: China

text: goose

text: gut metagenome

text: Caecal digesta of goose

text: Metagenome or environmental sample from gut metagenome


characteristic: ID

text: Chongqing Normal University

text: live

text: Plant

text: No applicable

characteristic: age

text: No applicable

characteristic: cultivar

text: Flowering stage

text: Wild-type

characteristic: ecotype

text: China: Chongqing

text: Root

characteristic: isolate

text: Perilla frutescens

text: No applicable

characteristic: tissue

text: Plant sample from Perilla frutescens


characteristic: External Id

text: Chongqing Normal University

characteristic: INSDC center name

characteristic: INSDC first public

characteristic: INSDC last update

text: live

text: Plant

text: No applicable

text: No applicable

text: Flowering stage

text: Wild-type

text: China: Chongqing

text: Stem

text: Perilla frutescens

text: No applicable

text: Plant sample from Perilla frutescens


text: Chongqing Normal University

text: live

characteristic: INSDC status

text: Plant

characteristic: NCBI submission model

text: No applicable

text: No applicable

text: Flowering stage

text: Wild-type

text: China: Chongqing

text: Leaf

text: Perilla frutescens

text: No applicable

text: Plant sample from Perilla frutescens


text: Chongqing Normal University

text: live

text: Plant

characteristic: NCBI submission package

text: No applicable

text: No applicable

text: Flowering stage

text: Wild-type

text: China: Chongqing

text: Flower

text: Perilla frutescens

text: No applicable

text: Plant sample from Perilla frutescens


text: Chongqing Normal University

text: live

text: Plant

text: No applicable

text: No applicable

text: Flowering stage

text: Wild-type

text: China: Chongqing

text: Seed

text: Perilla frutescens

text: No applicable

text: Plant sample from Perilla frutescens


text: Northeast Normal University

characteristic: INSDC secondary accession

text: live

text: Metagenome or environmental

characteristic: SRA accession

text: China:Guangdong

text: Hipposideros armiger

characteristic: host

text: 22 N 111 E

text: bat metagenome


text: Northeast Normal University

text: live

text: Metagenome or environmental

text: China:Guangdong

text: Hipposideros armiger

text: 24 N 113 E

text: bat metagenome

characteristic: organism

characteristic: title


text: Cepheid

text: live

text: Microbe, viral or environmental

text: Nigeria

text: Homo sapiens

text: Escherichia coli

text: isolate

characteristic: strain

text: Microbe sample from Escherichia coli


text: Cepheid

text: live

text: Microbe, viral or environmental

text: Nigeria

text: Homo sapiens

text: Klebsiella pneumoniae

text: isolate

text: Microbe sample from Klebsiella pneumoniae


text: Cepheid

text: live

text: Microbe, viral or environmental

text: Nigeria

text: Homo sapiens

text: Pseudomonas aeruginosa

text: isolate

text: Microbe sample from Pseudomonas aeruginosa


text: Henan University of Technology

text: live

text: Microbe, viral or environmental

text: China:Jiangsu

text: lake sediment

text: Pseudomonas

text: pure culture

text: Microbe sample from Pseudomonas


text: Anhui Science And Technology University

text: live

text: Metagenome or environmental

characteristic: Tmp

text: China:Anhui

text: Sus scrofa

text: duroc

text: pig metagenome


text: Anhui Science And Technology University

text: live

text: Metagenome or environmental

text: China:Anhui

text: Sus scrofa

text: Huai pig

text: pig metagenome


text: LANGEBIO

text: live

text: Microbe, viral or environmental

text: USA:Florida

text: Eumaeus atala

text: Gut

text: Pantoea sp. EA-12

text: Cell culture

text: Microbe sample from Pantoea sp. EA-12


text: LANGEBIO

text: live

text: Microbe, viral or environmental

text: USA:Florida

text: Eumaeus atala

text: Gut

text: Pantoea sp. EABMAA-21

text: Cell culture

text: Microbe sample from Pantoea sp. EABMAA-21


text: LANGEBIO

text: live

text: Microbe, viral or environmental

text: USA:Florida

text: Pharaxonotha floridana

text: Stenotrophomonas sp. PFBMAA-4

text: Cell culture

text: Microbe sample from Stenotrophomonas sp. PFBMAA-4


text: LANGEBIO

text: live

text: Microbe, viral or environmental

text: USA:Florida

text: Rhopalotria slossonae

text: Stenotrophomonas sp. RS-48

text: Cell culture

text: Microbe sample from Stenotrophomonas sp. RS-48


text: LANGEBIO

text: live

text: Microbe, viral or environmental

text: USA:Florida

text: Pharaxonotha floridana

text: Serratia sp. PF2-63

text: Cell culture

text: Microbe sample from Serratia sp. PF2-63


text: LANGEBIO

text: live

text: Microbe, viral or environmental

text: USA:Florida

text: Pharaxonotha floridana

text: Serratia sp. PF-27

text: Cell culture

text: Microbe sample from Serratia sp. PF-27


text: live

text: Metagenome or environmental

text: China

text: goose

text: gut metagenome

text: Caecal digesta of goose


text: Fujian Agriculture and Forestry University

text: live

text: Plant

text: mature

text: Fujian

characteristic: ecotype

text: China: Shuangli Village, Youxi County, Fujian Province

text: 26.12 N 118.04 E

text: Acorus calamus

text: stem

text: Plant sample from Acorus calamus


text: live

text: Plant

text: mature

text: Fujian

text: 26.12 N 118.04 E

text: Acorus calamus

text: root

text: Plant sample from Acorus calamus


text: live

text: Plant

text: mature

text: Fujian

text: 26.12 N 118.04 E

text: Acorus calamus

text: leaves

text: Plant sample from Acorus calamus


text: live

text: Plant

text: mature

text: Fujian

text: 26.12 N 118.04 E

text: Acorus calamus

text: flowers

text: Plant sample from Acorus calamus


text: live

text: Plant

text: mature

text: Fujian

text: 26.12 N 118.04 E

text: Acorus calamus

text: The lower part of the flower.

text: Plant sample from Acorus calamus


text: live

text: Plant

text: mature

text: Fujian

text: 26.12 N 118.04 E

text: Acorus calamus

text: Flower bottom

text: Plant sample from Acorus calamus


text: live

text: Plant

text: mature

text: Fujian

text: 26.12 N 118.04 E

text: Acorus calamus

text: Flower buds and leaf tips

text: Plant sample from Acorus calamus


R-Ata-InB

text: live

text: Plant

text: mature

text: Fujian

text: 26.12 N 118.04 E

text: Acorus gramineus

text: inflorescence

text: Plant sample from Acorus gramineus


R-Ata-FlB

text: live

text: Plant

text: mature

text: Fujian

text: 26.12 N 118.04 E

text: Acorus gramineus

text: flowers

text: Plant sample from Acorus gramineus


R-Ata-LeB

text: live

text: Plant

text: mature

text: Fujian

text: 26.12 N 118.04 E

text: Acorus gramineus

text: leaves

text: Plant sample from Acorus gramineus


R-Ata-StB

text: live

text: Plant

text: mature

text: Fujian

text: 26.12 N 118.04 E

text: Acorus gramineus

text: steam

text: Plant sample from Acorus gramineus


R-Ata-RoB

text: live

text: Plant

text: mature

text: Fujian

text: 26.12 N 118.04 E

text: Acorus gramineus

text: root

text: Plant sample from Acorus gramineus


R-Ata-FrB

text: live

text: Plant

text: mature

text: Fujian

text: 26.12 N 118.04 E

text: Acorus gramineus

text: infructescence

text: Plant sample from Acorus gramineus


R-Ata-FB

text: live

text: Plant

text: mature

text: Fujian

text: 26.12 N 118.04 E

text: Acorus gramineus

text: fruit

text: Plant sample from Acorus gramineus


Bhagwa

text: Indian Council of Agricultural Research

text: live

text: Plant

text: Bhagwa

characteristic: cultivar

text: Acc.1 resequencing

characteristic: description

text: Leaf

text: India

text: Punica granatum

text: Leaf

text: Resequencing of pomegranate genotypes


characteristic: External Id

text: Chinese Academy of Medical Sciences and Peking Union Medic

text: live

text: Plant

characteristic: age

text: replicate 3, 3 days, control

text: China:Beijing

text: Lycium barbarum

text: ungall

characteristic: tissue

text: Plant sample from Lycium barbarum


characteristic: INSDC center name

characteristic: INSDC first public

characteristic: INSDC last update

text: live

text: Plant

text: replicate 3, 3 days, treated

text: China:Beijing

text: Lycium barbarum

text: gall

text: Plant sample from Lycium barbarum


text: live

characteristic: INSDC status

text: Plant

characteristic: NCBI submission model

characteristic: NCBI submission package

text: replicate 3, 9 days, control

text: China:Beijing

text: Lycium barbarum

text: ungall

text: Plant sample from Lycium barbarum


characteristic: INSDC secondary accession

text: live

text: Plant

characteristic: SRA accession

text: replicate 3, 9 days, treated

text: China:Beijing

text: Lycium barbarum

text: gall

text: Plant sample from Lycium barbarum


text: live

text: Plant

text: replicate 3, 18 days, control

text: China:Beijing

text: Lycium barbarum

characteristic: organism

text: ungall

text: Plant sample from Lycium barbarum

characteristic: title


text: live

text: Plant

text: replicate 3, 18 days, treated

text: China:Beijing

text: Lycium barbarum

text: gall

text: Plant sample from Lycium barbarum


text: Hebei Academy of Agricultural and Forestry Sciences

text: live

text: Plant

text: 15 years

text: China

text: China:Shijiazhuang

text: Unbound bag of SF

characteristic: isolate

text: Malus domestica

text: peel

text: Plant sample from Malus domestica


text: live

text: Plant

text: 15 years

text: China

characteristic: ecotype

text: China:Shijiazhuang

text: Unpacking for 10 days of SF

text: Malus domestica

text: peel

text: Plant sample from Malus domestica


text: live

text: Plant

text: 15 years

characteristic: cultivar

text: China

text: China:Shijiazhuang

text: Complete coloring of SF

text: Malus domestica

text: peel

text: Plant sample from Malus domestica


text: live

text: Plant

text: 15 years

text: China

text: China:Shijiazhuang

text: Unbound bag of HM

text: Malus domestica

text: peel

text: Plant sample from Malus domestica


text: live

text: Plant

text: 15 years

text: China

text: China:Shijiazhuang

text: Unpacking for 10 days of HM

text: Malus domestica

text: peel

text: Plant sample from Malus domestica


text: live

text: Plant

text: 15 years

text: China

text: China:Shijiazhuang

text: Complete coloring of HM

text: Malus domestica

text: peel

text: Plant sample from Malus domestica


text: The Second Hospital of Hebei Medical University

text: live

text: Metagenome or environmental

text: China: Shijiazhuang

text: children

characteristic: host

text: feces

text: 38.03 N 114.26 E

text: feces metagenome

text: Metagenome or environmental sample from feces metagenome


characteristic: External Id

text: Chongqing Health Center for Women and Children

text: live

text: Model organism or animal

text: Mus musculus

text: not collected

characteristic: sex

text: 2-cell stage embryos

characteristic: treatment


Legionella pneumophila 1074

text: Russian Research Anti-Plague Institute Microbe

characteristic: INSDC center name

text: live

text: Microbe, viral or environmental

text: Russia: Astrakhan

text: hot water systems

text: Legionella pneumophila

text: cell culture

characteristic: strain

text: Microbe sample from Legionella pneumophila


Legionella pneumophila 1075

characteristic: INSDC first public

characteristic: INSDC last update

text: live

text: Microbe, viral or environmental

text: Russia: Astrakhan

text: hot water systems

text: Legionella pneumophila

text: cell culture


Pa-EAmG

text: LANGEBIO

text: live

characteristic: INSDC status

text: Microbe, viral or environmental

characteristic: NCBI submission model

text: USA:Florida

text: Eumaeus atala

text: Pantoea sp. Pa-EAmG

text: MAG

text: Pa-EAmG

text: Microbe sample from Pantoea sp. Pa-EAmG


Se-PFmG

text: LANGEBIO

text: live

text: Microbe, viral or environmental

characteristic: NCBI submission package

text: USA:Florida

text: Pharaxonotha floridana

text: Serratia bockelmannii

text: MAG

text: Se-PFmG

text: Microbe sample from Serratia bockelmannii


St-PFmG

text: LANGEBIO

text: live

text: Microbe, viral or environmental

text: USA:Florida

text: Pharaxonotha floridana

text: Stenotrophomonas sp. St-PFmG

text: MAG

text: St-PFmG

text: Microbe sample from Stenotrophomonas sp. St-PFmG


Se-PFBMAAmG

text: LANGEBIO

text: live

text: Microbe, viral or environmental

text: USA:Florida

text: Pharaxonotha floridana

text: Serratia sp. Se-PFBMAAmG

text: MAG

text: Se-PFBMAAmG

text: Microbe sample from Serratia sp. Se-PFBMAAmG


St-PFBMAAmG

text: LANGEBIO

text: live

text: Microbe, viral or environmental

text: USA:Florida

text: Pharaxonotha floridana

text: Stenotrophomonas sp. St-PFBMAAmG

text: MAG

text: St-PFBMAAmG

text: Microbe sample from Stenotrophomonas sp. St-PFBMAAmG


Se-RSmG

text: LANGEBIO

text: live

text: Microbe, viral or environmental

text: USA:Florida

text: Rhopalotria slossonae

text: Serratia sp. Se-RSmG

text: MAG

text: Se-RSmG

text: Microbe sample from Serratia sp. Se-RSmG


St-RSmG

text: LANGEBIO

text: live

text: Microbe, viral or environmental

text: USA:Florida

text: Rhopalotria slossonae

text: Stenotrophomonas sp. St-RSmG

text: MAG

text: St-RSmG

text: Microbe sample from Stenotrophomonas sp. St-RSmG


Se-RSBMAAmG

text: LANGEBIO

text: live

text: Microbe, viral or environmental

text: USA:Florida

text: Rhopalotria slossonae

text: Serratia sp. Se-RSBMAAmG

text: MAG

text: Se-RSBMAAmG

text: Microbe sample from Serratia sp. Se-RSBMAAmG


St-RSBMAAmG

text: LANGEBIO

text: live

text: Microbe, viral or environmental

text: USA:Florida

text: Rhopalotria slossonae

text: Stenotrophomonas sp. St-RSBMAAmG

text: MAG

text: St-RSBMAAmG

text: Microbe sample from Stenotrophomonas sp. St-RSBMAAmG


text: Huazhong Agricultural University

characteristic: INSDC secondary accession

text: live

text: Metagenome or environmental

characteristic: SRA accession

text: not collected

text: China:Wuxue

text: not collected

text: metagenome

text: biological replicate 1

characteristic: replicate

text: Metagenome or environmental sample from metagenome


text: Huazhong Agricultural University

text: live

text: Metagenome or environmental

text: not collected

text: China:Wuxue

text: not collected

text: metagenome

characteristic: organism

text: biological replicate 2

characteristic: title


text: Huazhong Agricultural University

text: live

text: Metagenome or environmental

text: not collected

text: China:Wuxue

text: not collected

text: metagenome

text: biological replicate 3


text: Huazhong Agricultural University

text: live

text: Metagenome or environmental

text: not collected

text: China:Wuxue

text: not collected

text: metagenome

text: biological replicate 4


text: Huazhong Agricultural University

text: live

text: Metagenome or environmental

text: not collected

text: China:JiNing

text: not collected

text: metagenome

text: biological replicate 1


text: Huazhong Agricultural University

text: live

text: Metagenome or environmental

text: not collected

text: China:JiNing

text: not collected

text: metagenome

text: biological replicate 2


text: Huazhong Agricultural University

text: live

text: Metagenome or environmental

text: not collected

text: China:JiNing

text: not collected

text: metagenome

text: biological replicate 3


text: Huazhong Agricultural University

text: live

text: Metagenome or environmental

text: not collected

text: China:JiNing

text: not collected

text: metagenome

text: biological replicate 4


text: Huazhong Agricultural University

text: live

text: Metagenome or environmental

text: not collected

text: China:HaiLun

text: not collected

text: metagenome

text: biological replicate 1


text: Huazhong Agricultural University

text: live

text: Metagenome or environmental

text: not collected

text: China:HaiLun

text: not collected

text: metagenome

text: biological replicate 2


text: Huazhong Agricultural University

text: live

text: Metagenome or environmental

text: not collected

text: China:HaiLun

text: not collected

text: metagenome

text: biological replicate 3


text: Huazhong Agricultural University

text: live

text: Metagenome or environmental

text: not collected

text: China:HaiLun

text: not collected

text: metagenome

text: biological replicate 4


text: Huazhong Agricultural University

text: live

text: Metagenome or environmental

text: not collected

text: China:QiYang

text: not collected

text: metagenome

text: biological replicate 1


text: Huazhong Agricultural University

text: live

text: Metagenome or environmental

text: not collected

text: China:QiYang

text: not collected

text: metagenome

text: biological replicate 2


text: Huazhong Agricultural University

text: live

text: Metagenome or environmental

text: not collected

text: China:QiYang

text: not collected

text: metagenome

text: biological replicate 3


text: Huazhong Agricultural University

text: live

text: Metagenome or environmental

text: not collected

text: China:QiYang

text: not collected

text: metagenome

text: biological replicate 4


Escherichia coli AVS0093

text: University of Zurich

text: live

text: Pathogen.env

text: Amt fuer Verbraucherschutz, Kanton Zug

text: Switzerland: Kanton Zug

text: environmental-WWTP

text: Escherichia coli

text: Pathogen: environmental/food/other sample from Escherichia coli


Escherichia coli AVS0467

text: University of Zurich

text: live

text: Pathogen.env

text: Amt fuer Verbraucherschutz, Kanton Zug

text: Switzerland: Kanton Zug

text: environmental-WWTP

text: Escherichia coli


Escherichia coli AVS0171

text: University of Zurich

text: live

text: Pathogen.env

text: Amt fuer Verbraucherschutz, Kanton Zug

text: Switzerland: Kanton Zug

text: environmental-WWTP

text: Escherichia coli


Escherichia coli AVS0226

text: University of Zurich

text: live

text: Pathogen.env

text: Amt fuer Verbraucherschutz, Kanton Zug

text: Switzerland: Kanton Zug

text: environmental-WWTP

text: Escherichia coli


Escherichia coli AVS0362

text: University of Zurich

text: live

text: Pathogen.env

text: Amt fuer Verbraucherschutz, Kanton Zug

text: Switzerland: Kanton Zug

text: environmental-WWTP

text: Escherichia coli


Escherichia coli AVS0453

text: University of Zurich

text: live

text: Pathogen.env

text: Amt fuer Verbraucherschutz, Kanton Zug

text: Switzerland: Kanton Zug

text: environmental-WWTP

text: Escherichia coli


Escherichia coli AVS0283

text: University of Zurich

text: live

text: Pathogen.env

text: Amt fuer Verbraucherschutz, Kanton Zug

text: Switzerland: Kanton Zug

text: wastewater

text: Escherichia coli


Escherichia coli AVS0530

text: University of Zurich

text: live

text: Pathogen.env

text: Amt fuer Verbraucherschutz, Kanton Zug

text: Switzerland: Kanton Zug

text: wastewater

text: Escherichia coli


Escherichia coli AVS0533

text: University of Zurich

text: live

text: Pathogen.env

text: Amt fuer Verbraucherschutz, Kanton Zug

text: Switzerland: Kanton Zug

text: wastewater

text: Escherichia coli


Escherichia coli AVS0710

text: University of Zurich

text: live

text: Pathogen.env

text: Amt fuer Verbraucherschutz, Kanton Zug

text: Switzerland: Kanton Zug

text: wastewater

text: Escherichia coli


Escherichia coli AVS0713

text: University of Zurich

text: live

text: Pathogen.env

text: Amt fuer Verbraucherschutz, Kanton Zug

text: Switzerland: Kanton Zug

text: wastewater

text: Escherichia coli


Escherichia coli AVS0971

text: University of Zurich

text: live

text: Pathogen.env

text: Amt fuer Verbraucherschutz, Kanton Zug

text: Switzerland: Kanton Zug

text: wastewater

text: Escherichia coli


Escherichia coli AVS0786

text: University of Zurich

text: live

text: Pathogen.env

text: Amt fuer Verbraucherschutz, Kanton Zug

text: Switzerland: Kanton Zug

text: wastewater

text: Escherichia coli


Escherichia coli AVS0753

text: University of Zurich

text: live

text: Pathogen.env

text: Amt fuer Verbraucherschutz, Kanton Zug

text: Switzerland: Kanton Zug

text: wastewater

text: Escherichia coli


Escherichia coli AVS0787

text: University of Zurich

text: live

text: Pathogen.env

text: Amt fuer Verbraucherschutz, Kanton Zug

text: Switzerland: Kanton Zug

text: wastewater

text: Escherichia coli


Escherichia coli AVS0285

text: University of Zurich

text: live

text: Pathogen.env

text: Amt fuer Verbraucherschutz, Kanton Zug

text: Switzerland: Kanton Zug

text: wastewater treatment plant efflux

text: Escherichia coli


Escherichia coli AVS0536

text: University of Zurich

text: live

text: Pathogen.env

text: Amt fuer Verbraucherschutz, Kanton Zug

text: Switzerland: Kanton Zug

text: wastewater treatment plant efflux

text: Escherichia coli


Escherichia coli AVS0717

text: University of Zurich

text: live

text: Pathogen.env

text: Amt fuer Verbraucherschutz, Kanton Zug

text: Switzerland: Kanton Zug

text: wastewater treatment plant efflux

text: Escherichia coli


Escherichia coli AVS0754

text: University of Zurich

text: live

text: Pathogen.env

text: Amt fuer Verbraucherschutz, Kanton Zug

text: Switzerland: Kanton Zug

text: wastewater treatment plant efflux

text: Escherichia coli


text: Fujian Provincial Maternity and Child Health Hospital

text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 628-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

characteristic: isolate

text: Homo sapiens

text: female

text: chorionic villi

characteristic: tissue

text: Human sample from Homo sapiens


characteristic: External Id

text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 629-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 630-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

characteristic: sex

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 631-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 632-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 633-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 634-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 635-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 636-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 637-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 638-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 639-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 640-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 641-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 642-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 643-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: Fujian Provincial Maternity and Child Health Hospital

text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 644-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 645-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 646-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 647-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 648-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 649-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 650-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 651-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 652-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 653-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 654-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 655-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 656-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 657-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 658-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 659-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: Fujian Provincial Maternity and Child Health Hospital

text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 660-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 661-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 662-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 663-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 664-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 665-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 666-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 667-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 668-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 669-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 670-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 671-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 672-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 673-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 674-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 675-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: Fujian Provincial Maternity and Child Health Hospital

text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 676-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 677-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 678-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 679-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 680-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 681-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 682-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 683-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 684-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 685-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 686-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 687-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 688-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 689-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 690-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 691-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: Fujian Provincial Maternity and Child Health Hospital

text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 692-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 693-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 694-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 695-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 696-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 697-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 698-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 699-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 700-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 701-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 702-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 703-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 704-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 705-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 706-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 707-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: Fujian Provincial Maternity and Child Health Hospital

text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 708-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 709-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens