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text: hCoV-19/Switzerland/TI-EOC-22_28602694/2024

characteristic: isolate

characteristic: organism

characteristic: sample capture status


characteristic: ENA-LAST-UPDATE

characteristic: External Id

text: Laboratorio di Microbiologia, Dipartimento di Medicina di Laboratorio EOLAB, Ente Ospedaliero Cantonale, Bellinzona, Switzerland

characteristic: INSDC center name

characteristic: INSDC first public

text: public

characteristic: Submitter Id

text: SIB

characteristic: collection date

text: Switzerland

characteristic: geographic location (country and/or sea)

text: TI

characteristic: geographic location (region and locality)

text: Human

text: restricted access

text: Homo sapiens

text: restricted access

text: restricted access

text: hCoV-19/Switzerland/TI-EOC-42_28625599/2024

characteristic: title


characteristic: ENA-CHECKLIST

characteristic: ENA-FIRST-PUBLIC

characteristic: INSDC last update

text: public

characteristic: INSDC status

characteristic: SRA accession

text: SIB

characteristic: broker name

characteristic: collecting institution

text: Martinetti Lucchini Gladys, Valeria Spina, Gloria Gaudio

characteristic: collector name

text: Switzerland

text: TI

text: Human

characteristic: host common name

text: restricted access

text: Homo sapiens

text: restricted access

text: restricted access

text: hCoV-19/Switzerland/TI-EOC-42_28619047/2024


characteristic: ENA-LAST-UPDATE

characteristic: External Id

text: public

text: SIB

text: Switzerland

text: TI

text: Human

text: restricted access

characteristic: host health state

text: Homo sapiens

characteristic: host scientific name

text: restricted access

characteristic: host sex

text: restricted access

characteristic: host subject id

text: hCoV-19/Switzerland/TI-EOC-12_28616087/2024

characteristic: isolate

characteristic: organism

characteristic: sample capture status


characteristic: ENA-CHECKLIST

characteristic: ENA-FIRST-PUBLIC

characteristic: INSDC center name

characteristic: INSDC first public

text: public

characteristic: Submitter Id

text: SIB

text: Valais Hospital, Central Institute; Sion, Switzerland

characteristic: collection date

text: Switzerland

characteristic: geographic location (country and/or sea)

text: VS

characteristic: geographic location (region and locality)

text: Human

text: restricted access

text: Homo sapiens

text: restricted access

text: restricted access

text: hCoV-19/Switzerland/VS-ICH-2240104728/2024

characteristic: title


characteristic: ENA-LAST-UPDATE

characteristic: External Id

characteristic: INSDC last update

text: public

characteristic: INSDC status

characteristic: SRA accession

text: SIB

characteristic: broker name

characteristic: collecting institution

text: Alexis Dumoulin, Lorenzo Cerutti, Cedric Howald, Henri Pegeot, Melyssa Elies, Deborah Penet, Keith Harshman, Ioannis Xenarios

characteristic: collector name

text: Switzerland

text: VS

text: Human

characteristic: host common name

text: restricted access

text: Homo sapiens

text: restricted access

text: restricted access

text: hCoV-19/Switzerland/VS-ICH-2240101823/2024


characteristic: ENA-CHECKLIST

characteristic: ENA-FIRST-PUBLIC

text: public

text: SIB

text: Switzerland

text: VS

text: Human

text: restricted access

characteristic: host health state

text: Homo sapiens

characteristic: host scientific name

text: restricted access

characteristic: host sex

text: restricted access

characteristic: host subject id

text: hCoV-19/Switzerland/VS-ICH-2240102804/2024

characteristic: isolate

characteristic: organism

characteristic: sample capture status


characteristic: ENA-LAST-UPDATE

characteristic: External Id

characteristic: INSDC center name

characteristic: INSDC first public

text: public

characteristic: Submitter Id

text: SIB

characteristic: collection date

text: Switzerland

characteristic: geographic location (country and/or sea)

text: TI

characteristic: geographic location (region and locality)

text: Human

text: restricted access

text: Homo sapiens

text: restricted access

text: restricted access

text: hCoV-19/Switzerland/TI-EOC-22_28604666/2024

text: Severe acute respiratory syndrome coronavirus 2

characteristic: title


characteristic: ENA-CHECKLIST

characteristic: ENA-FIRST-PUBLIC

text: UNIVERSITY OF HELSINKI

characteristic: INSDC last update

text: public

characteristic: INSDC status

characteristic: SRA accession

tag: Namespace:UNIVERSITY OF HELSINKI

text: Human gut

characteristic: broad-scale environmental context

characteristic: description

text: Feces

characteristic: environmental medium

text: Finland

characteristic: geographic location (latitude)

characteristic: geographic location (longitude)

text: Human gut

characteristic: local environmental context

text: human gut metagenome

text: Infant gut microbiot and allergic diseases

characteristic: project name

text: human gut metagenome


characteristic: ENA-LAST-UPDATE

characteristic: External Id

text: Scripps Institution of Oceanography

characteristic: INSDC center name

characteristic: INSDC first public

text: public

text: ena-SAMPLE-TAB-29-01-2024-17:24:33:780-60101

tag: Namespace:Scripps Institution of Oceanography

characteristic: Submitter Id

text: metagenome assembled genome of Candidatus�Xenohaliotis californiensis, causative agent of withering syndrome

text: USA

text: diseased

characteristic: host health state

text: Haliotis sorenseni

characteristic: host scientific name

text: 2 abalone samples

characteristic: isolate

text: white abalone

text: Candidatus Xenohaliotis californiensis

characteristic: organism

text: Candidatus Xenohaliotis californiensis

text: CaXc MAG


characteristic: ENA-CHECKLIST

characteristic: ENA-FIRST-PUBLIC

text: Anthony Smith, NICD

characteristic: INSDC last update

text: public

characteristic: INSDC status

characteristic: SRA accession

tag: Namespace:Anthony Smith, NICD

text: EnteroBase

characteristic: broker name

text: EnteroBase

text: A. Smith, National Institute for Communicable Diseases

characteristic: collection date

text: Whole genome sequencing data uploaded by EnteroBase user

text: South Africa

characteristic: geographic location (country and/or sea)

text: KwaZulu-Natal

characteristic: geographic location (region and locality)

text: Human, Blood culture

text: Salmonella enterica

text: Salmonella enterica

text: Typhi

characteristic: serovar

characteristic: strain

characteristic: title


characteristic: ENA-LAST-UPDATE

characteristic: External Id

text: Anthony Smith, NICD

characteristic: INSDC center name

characteristic: INSDC first public

text: public

characteristic: Submitter Id

text: EnteroBase

text: EnteroBase

characteristic: description

text: South Africa

text: Gauteng

text: Human, Blood culture

text: Salmonella enterica

text: Salmonella enterica

text: Typhi


characteristic: ENA-CHECKLIST

characteristic: ENA-FIRST-PUBLIC

text: Anthony Smith, NICD

text: public

text: EnteroBase

text: EnteroBase

text: South Africa

text: Gauteng

text: Human, Stool

text: Salmonella enterica

characteristic: organism

text: Salmonella enterica

text: Typhi


text: Anthony Smith, NICD

characteristic: INSDC last update

text: public

characteristic: INSDC status

characteristic: SRA accession

text: EnteroBase

text: EnteroBase

text: South Africa

text: Limpopo

text: Human, Stool

text: Vibrio cholerae

text: Vibrio cholerae


text: Anthony Smith, NICD

text: public

text: EnteroBase

characteristic: broker name

text: EnteroBase

characteristic: collection date

text: South Africa

characteristic: geographic location (country and/or sea)

text: Gauteng

text: Human, Stool

text: Vibrio cholerae

text: Vibrio cholerae


E-MTAB-13743:Sample 1

text: NMBU

text: public

text: E-MTAB-13743:Sample 1

unit: week

characteristic: age

text: ArrayExpress

text: not collected

text: Atlantic salmon

characteristic: common name

text: Protocols: Fish were euthanized by a blow to the head and samples of liver were cut into ~5 mm cubes and placed in RNAlater. Samples were incubated for at least 30 minutes at room temperature before long-term storage at -20°C. Atlantic salmon eggs, provided by AquaGen Breeding Centre Kyrksæterøra, Norway, were sterilized at the Norwegian University of Life Sciences (NMBU) fish lab and incubated at 350 to 372 day-degrees until hatching. First feeding of fry took place 5 weeks after hatching. Fry were then randomly divided into two replicate tanks and reared on a standard commercial diet high in EPA and DHA. Sampling began at 21 weeks after first feeding (week 1), and again 10, 19, and 25 weeks after that. One week after the first sampling a portion of fish from each tank were transferred to replicate light control tanks and sampled in the same manner as the experimental fish. At the same time, the experimental fish were switched to “winter-like” lighting conditions with 8 hours of light per day for 8 weeks to trigger smoltification, before returning to “spring-like” conditions with 24 hours of light per day. Immediately after the week 19 sampling, a portion of fish from each tank were transferred to seawater conditions at the Norwegian Institute for Water Research (NIVA), Solbergstranda, Norway. UV-sterilized seawater used in this life-stage had a salinity of 3%-3.5% and was obtained from the Oslofjord. Fish were sedated before transport and allowed to acclimatize for several hours before being slowly introduced to the new water conditions. The fish that were not transferred to seawater were sampled as a freshwater control at the same time as the experimental fish. The liver tissues were washed and perfused with cold PBS to remove blood before being dissociated and strained through a cell strainer. The nuclei were isolated from cell homogenate by centrifugation and counted on an automated cell counter (TC20 BioRad, range 4-6 um). Transposition of 100k (weeks 1, 19 and 25) and 75k (week 10) nuclei was performed by Tn5 transposase from Nextera DNA Library Preparation kit. The resulting DNA fragments were purified and stored at -20°C. PCR Amplification with addition of sequencing indexes (Nextera DNA CD) were done according to Buenrostro et al. 2015, with a test PCR performed to determine the correct number of amplification cycles. The ATAC libraries were cleaned by Ampure XP beads and assessed by BioAnalyser (Agilent) using High sensitivity chips. Quantity of libraries were determined by using Qubit Fluorometer (Thermo). Mean insert size for the libraries was 190 bp.

text: juvenile, pre-smoltification

characteristic: developmental stage

text: wild type genotype

characteristic: genotype

text: not collected

characteristic: individual

text: not applicable

characteristic: isolate

text: Salmo salar

text: Salmo salar

text: liver

characteristic: organism part

text: Salmo salar

text: not available

characteristic: sex

text: AquaGen

characteristic: strain

text: Sample 1


E-MTAB-13743:Sample 2

characteristic: ENA-CHECKLIST

characteristic: ENA-FIRST-PUBLIC

characteristic: ENA-LAST-UPDATE

characteristic: External Id

text: NMBU

characteristic: INSDC center name

characteristic: INSDC first public

text: public

text: E-MTAB-13743:Sample 2

characteristic: Submitter Id

text: ArrayExpress

text: not collected

text: Atlantic salmon

characteristic: description

text: juvenile, pre-smoltification

text: wild type genotype

text: not collected

text: not applicable

text: Salmo salar

text: Salmo salar

text: liver

text: Salmo salar

text: not available

text: AquaGen

text: Sample 2

characteristic: title


E-MTAB-13743:Sample 3

text: NMBU

characteristic: INSDC last update

text: public

characteristic: INSDC status

characteristic: SRA accession

text: E-MTAB-13743:Sample 3

characteristic: age

text: ArrayExpress

characteristic: broker name

text: not collected

characteristic: collection date

text: Atlantic salmon

characteristic: common name

text: juvenile, pre-smoltification

text: wild type genotype

text: not collected

characteristic: geographic location (country and/or sea)

text: not applicable

text: Salmo salar

characteristic: organism

text: Salmo salar

text: liver

text: Salmo salar

text: not available

text: AquaGen

text: Sample 3


E-MTAB-13743:Sample 4

characteristic: ENA-CHECKLIST

characteristic: ENA-FIRST-PUBLIC

text: NMBU

text: public

text: E-MTAB-13743:Sample 4

text: ArrayExpress

text: not collected

text: Atlantic salmon

text: juvenile, pre-smoltification

characteristic: developmental stage

text: wild type genotype

characteristic: genotype

text: not collected

characteristic: individual

text: not applicable

characteristic: isolate

text: Salmo salar

text: Salmo salar

text: liver

characteristic: organism part

text: Salmo salar

text: not available

characteristic: sex

text: AquaGen

characteristic: strain

text: Sample 4


E-MTAB-13743:Sample 5

characteristic: ENA-LAST-UPDATE

characteristic: External Id

text: NMBU

characteristic: INSDC center name

characteristic: INSDC first public

characteristic: INSDC last update

text: public

characteristic: INSDC status

text: E-MTAB-13743:Sample 5

characteristic: Submitter Id

text: ArrayExpress

text: not collected

text: Atlantic salmon

characteristic: description

text: adult, post-smoltification

text: wild type genotype

text: not collected

text: not applicable

text: Salmo salar

text: Salmo salar

text: liver

text: Salmo salar

text: not available

text: AquaGen

text: Sample 5

characteristic: title


E-MTAB-13743:Sample 6

characteristic: ENA-CHECKLIST

characteristic: ENA-FIRST-PUBLIC

text: NMBU

text: public

characteristic: SRA accession

text: E-MTAB-13743:Sample 6

characteristic: age

text: ArrayExpress

characteristic: broker name

text: not collected

characteristic: collection date

text: Atlantic salmon

characteristic: common name

text: adult, post-smoltification

text: wild type genotype

text: not collected

characteristic: geographic location (country and/or sea)

text: not applicable

text: Salmo salar

characteristic: organism

text: Salmo salar

text: liver

text: Salmo salar

text: not available

text: AquaGen

text: Sample 6


E-MTAB-13743:Sample 7

characteristic: ENA-LAST-UPDATE

characteristic: External Id

text: NMBU

text: public

text: E-MTAB-13743:Sample 7

text: ArrayExpress

text: not collected

text: Atlantic salmon

text: adult, post-smoltification

characteristic: developmental stage

text: wild type genotype

characteristic: genotype

text: not collected

characteristic: individual

text: not applicable

characteristic: isolate

text: Salmo salar

text: Salmo salar

text: liver

characteristic: organism part

text: Salmo salar

text: not available

characteristic: sex

text: AquaGen

characteristic: strain

text: Sample 7


E-MTAB-13743:Sample 8

characteristic: ENA-CHECKLIST

characteristic: ENA-FIRST-PUBLIC

text: NMBU

characteristic: INSDC center name

characteristic: INSDC first public

characteristic: INSDC last update

text: public

characteristic: INSDC status

text: E-MTAB-13743:Sample 8

characteristic: Submitter Id

text: ArrayExpress

text: not collected

text: Atlantic salmon

characteristic: description

text: adult, post-smoltification

text: wild type genotype

text: not collected

text: not applicable

text: Salmo salar

text: Salmo salar

text: liver

text: Salmo salar

text: not available

text: AquaGen

text: Sample 8

characteristic: title


characteristic: ENA-LAST-UPDATE

characteristic: External Id

text: public

characteristic: SRA accession

tag: Namespace:Department of Developmental Biology and Genetics

text: ArrayExpress

characteristic: broker name

text: epithelial cell

text: not collected

characteristic: collection date

text: human

characteristic: common name

text: Protocols: Cells were collected in the TRIzol reagent and lysed by repetitive pipetting. Cells were incubated at 37°C, 5% CO2, and 95% humidity. Empty vector control in Caco-2 cells by lentiviral vector-based transduction. Qiagen RNeasyMini Kit according to the manufacturer instructions. Total RNA was isolated and sent for RNAseq analysis The RNA quality assessment is done using RNA screen Tape system. RNA concentration is determined in a Qubit.3 Fluorometer using the Qubit RNA BR assay kit. The fragmented mRNAs were primed with random hexamers, and then reverse transcribed to form cDNA. The cDNA fragments obtained were cleaned up by using AM pure beads. The DNA underwent end repair wherein the mix converts the overhangs resulting from fragmentation into blunt ends. The samples were further purified using AMPure beads and The DNA was then enriched by PCR using illumina universal primer and sample-specific octamer primers. The amplified products were cleaned up by using AM pure beads and the final mRNA library was eluted.

text: adult

text: colorectal adenocarcinoma

characteristic: disease

text: empty vector

text: not collected

characteristic: geographic location (country and/or sea)

text: not applicable

text: Homo sapiens

characteristic: organism

text: Homo sapiens

text: large intestine

text: Homo sapiens


characteristic: ENA-CHECKLIST

characteristic: ENA-FIRST-PUBLIC

text: Department of Developmental Biology and Genetics

text: public

text: ArrayExpress

text: epithelial cell

text: not collected

text: human

text: adult

characteristic: developmental stage

text: colorectal adenocarcinoma

text: empty vector

characteristic: genotype

text: not collected

text: not applicable

characteristic: isolate

text: Homo sapiens

text: Homo sapiens

text: large intestine

characteristic: organism part

text: Homo sapiens


characteristic: INSDC center name

characteristic: INSDC first public

characteristic: INSDC last update

text: public

characteristic: INSDC status

characteristic: Submitter Id

text: ArrayExpress

text: epithelial cell

text: not collected

text: human

text: Protocols: Cells were collected in the TRIzol reagent and lysed by repetitive pipetting. Cells were incubated at 37°C, 5% CO2, and 95% humidity. Expression of NHE9 in Caco-2 cells by lentiviral vector based transduction. Qiagen RNeasyMini Kit according to the manufacturer instructions. Total RNA was isolated and sent for RNAseq analysis The RNA quality assessment is done using RNA screen Tape system. RNA concentration is determined in a Qubit.3 Fluorometer using the Qubit RNA BR assay kit. The fragmented mRNAs were primed with random hexamers, and then reverse transcribed to form cDNA. The cDNA fragments obtained were cleaned up by using AM pure beads. The DNA underwent end repair wherein the mix converts the overhangs resulting from fragmentation into blunt ends. The samples were further purified using AMPure beads and The DNA was then enriched by PCR using illumina universal primer and sample-specific octamer primers. The amplified products were cleaned up by using AM pure beads and the final mRNA library was eluted.

characteristic: description

text: adult

text: colorectal adenocarcinoma

text: NHE9 expression

text: not collected

text: not applicable

text: Homo sapiens

text: Homo sapiens

text: large intestine

text: Homo sapiens


characteristic: ENA-LAST-UPDATE

characteristic: External Id

text: WEHI

text: public

characteristic: SRA accession

text: GPRTG

characteristic: collection date

text: Globin LV sequenced with nanopore direct RNA technology

text: Switzerland

text: synthetic RNA

text: synthetic RNA

characteristic: title


characteristic: ENA-CHECKLIST

text: WEHI

text: public

text: GPRTG

text: Globin LV sequenced with nanopore direct cDNA technology

text: Switzerland

characteristic: geographic location (country and/or sea)

text: synthetic RNA

characteristic: organism

text: synthetic RNA


characteristic: ENA-FIRST-PUBLIC

text: WEHI

text: public

text: GPRTG

text: Globin LV sequenced with PacBio cDNA technology

text: Switzerland

text: synthetic RNA

text: synthetic RNA


text: WEHI

text: public

text: GPRTG

text: WAS LV1 sequenced with nanopore direct RNA technology

text: Switzerland

text: synthetic RNA

text: synthetic RNA


text: WEHI

text: public

text: GPRTG

text: WAS LV2 sequenced with nanopore direct RNA technology

text: Switzerland

text: synthetic RNA

text: synthetic RNA


text: WEHI

text: public

text: GPRTG

text: WAS LV3 sequenced with nanopore direct RNA technology

text: Switzerland

text: synthetic RNA

text: synthetic RNA


text: WEHI

text: public

text: GPRTG

text: WAS LV4 sequenced with nanopore direct RNA technology

text: Switzerland

text: synthetic RNA

text: synthetic RNA


text: WEHI

text: public

text: GPRTG

text: WAS LV5 sequenced with nanopore direct RNA technology

text: Switzerland

text: synthetic RNA

text: synthetic RNA


text: WEHI

text: public

text: GPRTG

text: WAS LV6 sequenced with nanopore direct RNA technology

text: Switzerland

text: synthetic RNA

text: synthetic RNA


text: WEHI

text: public

text: GPRTG

text: RNase treated WAS sequenced with nanopore direct RNA technology

text: Switzerland

text: synthetic RNA

text: synthetic RNA


text: WEHI

text: public

text: GPRTG

text: Untreated control sequenced with nanopore direct RNA technology

text: Switzerland

text: synthetic RNA

text: synthetic RNA


text: WEHI

text: public

text: GPRTG

text: Artificially polyadenylated WAS LV1 sequenced with nanopore direct RNA technology

text: Switzerland

text: synthetic RNA

text: synthetic RNA


text: WEHI

text: public

text: GPRTG

text: Artificially polyadenylated WAS LV2 sequenced with nanopore direct RNA technology

text: Switzerland

text: synthetic RNA

text: synthetic RNA


text: Cantacuzino NIMMRD

text: public

tag: Namespace:Cantacuzino NIMMRD

text: not provided

text: Romania

text: Homo sapiens

characteristic: host

text: Yes

text: stool

text: Escherichia coli

text: Escherichia coli


text: public

tag: Namespace:Laboratory of genomics and metagenomics, Institute of Microbiology, University Hospital Centre and University of Lausanne, Switzerland

text: SIB

characteristic: broker name

text: Hôpital Cantonal de Fribourg - HFR, CH-1752 Villars-sur-Glâne, Switzerland

characteristic: collecting institution

text: Trestan Pillonel, Damien Jacot, Sébastien Aeby, Gilbert Greub, Claire Bertelli

characteristic: collector name

text: Switzerland

text: VD

characteristic: geographic location (region and locality)

text: Human

characteristic: host common name

text: restricted access

characteristic: host health state

text: Homo sapiens

characteristic: host scientific name

text: restricted access

characteristic: host sex

text: restricted access

characteristic: host subject id

text: hCoV-19/Switzerland/VD-CHUV-GEN19206/2024

characteristic: isolate

text: Severe acute respiratory syndrome coronavirus 2

text: active surveillance not initiated by an outbreak

characteristic: sample capture status


characteristic: ENA-LAST-UPDATE

characteristic: External Id

text: Laboratory of genomics and metagenomics, Institute of Microbiology, University Hospital Centre and University of Lausanne, Switzerland

characteristic: INSDC center name

characteristic: INSDC first public

characteristic: INSDC last update

text: public

characteristic: INSDC status

characteristic: SRA accession

characteristic: Submitter Id

text: SIB

characteristic: collection date

text: Switzerland

text: VD

text: Human

text: restricted access

text: Homo sapiens

text: restricted access

text: restricted access

text: hCoV-19/Switzerland/VD-CHUV-GEN19209/2024

characteristic: title


characteristic: ENA-CHECKLIST

characteristic: ENA-FIRST-PUBLIC

text: public

text: SIB

characteristic: broker name

text: CHUV, CH-1011 Lausanne, Switzerland

characteristic: collecting institution

characteristic: collector name

text: Switzerland

characteristic: geographic location (country and/or sea)

text: VD

characteristic: geographic location (region and locality)

text: Human

characteristic: host common name

text: restricted access

text: Homo sapiens

text: restricted access

text: restricted access

text: hCoV-19/Switzerland/VD-CHUV-GEN19166/2024

characteristic: organism


characteristic: ENA-LAST-UPDATE

characteristic: External Id

characteristic: INSDC center name

text: public

text: SIB

text: CHUV, CH-1011 Lausanne, Switzerland

text: Switzerland

text: VD

text: Human

text: restricted access

characteristic: host health state

text: Homo sapiens

characteristic: host scientific name

text: restricted access

characteristic: host sex

text: restricted access

characteristic: host subject id

text: hCoV-19/Switzerland/VD-CHUV-GEN19192/2024

characteristic: isolate

characteristic: sample capture status


characteristic: ENA-CHECKLIST

characteristic: ENA-FIRST-PUBLIC

characteristic: INSDC first public

characteristic: INSDC last update

text: public

characteristic: INSDC status

characteristic: SRA accession

characteristic: Submitter Id

text: SIB

text: CHUV, CH-1011 Lausanne, Switzerland

characteristic: collection date

text: Switzerland

text: VD

text: Human

text: restricted access

text: Homo sapiens

text: restricted access

text: restricted access

text: hCoV-19/Switzerland/VD-CHUV-GEN19211/2024

characteristic: title


characteristic: ENA-LAST-UPDATE

characteristic: External Id

text: public

text: SIB

characteristic: broker name

characteristic: collecting institution

characteristic: collector name

text: Switzerland

characteristic: geographic location (country and/or sea)

text: VD

characteristic: geographic location (region and locality)

text: Human

characteristic: host common name

text: restricted access

text: Homo sapiens

text: restricted access

text: restricted access

text: hCoV-19/Switzerland/VD-CHUV-GEN19170/2024

characteristic: organism


characteristic: ENA-CHECKLIST

characteristic: ENA-FIRST-PUBLIC

characteristic: INSDC center name

text: public

text: SIB

text: CHUV, CH-1011 Lausanne, Switzerland

text: Switzerland

text: VD

text: Human

text: restricted access

characteristic: host health state

text: Homo sapiens

characteristic: host scientific name

text: restricted access

characteristic: host sex

text: restricted access

characteristic: host subject id

text: hCoV-19/Switzerland/VD-CHUV-GEN19167/2024

characteristic: isolate

characteristic: sample capture status


characteristic: ENA-LAST-UPDATE

characteristic: External Id

characteristic: INSDC first public

characteristic: INSDC last update

text: public

characteristic: INSDC status

characteristic: SRA accession

characteristic: Submitter Id

text: SIB

text: CHUV, CH-1011 Lausanne, Switzerland

characteristic: collection date

text: Switzerland

text: VD

text: Human

text: restricted access

text: Homo sapiens

text: restricted access

text: restricted access

text: hCoV-19/Switzerland/VD-CHUV-GEN19176/2024

characteristic: title


characteristic: ENA-CHECKLIST

characteristic: ENA-FIRST-PUBLIC

text: public

text: SIB

characteristic: broker name

text: CHUV, CH-1011 Lausanne, Switzerland

characteristic: collecting institution

characteristic: collector name

text: Switzerland

characteristic: geographic location (country and/or sea)

text: VD

characteristic: geographic location (region and locality)

text: Human

characteristic: host common name

text: restricted access

text: Homo sapiens

text: restricted access

text: restricted access

text: hCoV-19/Switzerland/VD-CHUV-GEN19202/2024

characteristic: organism


characteristic: ENA-LAST-UPDATE

characteristic: External Id

characteristic: INSDC center name

text: public

text: SIB

text: CHUV, CH-1011 Lausanne, Switzerland

text: Switzerland

text: VD

text: Human

text: restricted access

characteristic: host health state

text: Homo sapiens

characteristic: host scientific name

text: restricted access

characteristic: host sex

text: restricted access

characteristic: host subject id

text: hCoV-19/Switzerland/VD-CHUV-GEN19196/2024

characteristic: isolate

characteristic: sample capture status


characteristic: ENA-CHECKLIST

characteristic: ENA-FIRST-PUBLIC

characteristic: INSDC first public

characteristic: INSDC last update

text: public

characteristic: INSDC status

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