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 710-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


status: PUBLIC

characteristic: External Id

text: Fujian Provincial Maternity and Child Health Hospital

characteristic: INSDC center name

characteristic: INSDC first public

characteristic: INSDC last update

characteristic: INSDC secondary accession

text: live

characteristic: INSDC status

text: Human

characteristic: NCBI submission model

characteristic: NCBI submission package

characteristic: SRA accession

text: Yifang Dai

tag: attribute

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 711-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

characteristic: organism

text: female

characteristic: sex

text: chorionic villi

characteristic: tissue

text: Human sample from Homo sapiens

characteristic: title


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 712-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 713-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 714-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 715-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 716-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 717-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 718-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 719-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 720-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 721-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 722-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 723-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 724-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 725-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 726-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 727-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 728-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 729-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 730-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 731-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 732-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 733-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 734-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 735-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 736-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 737-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 738-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 739-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 740-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 741-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 742-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 743-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 744-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 745-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 746-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 747-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 748-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 749-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 750-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 751-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 752-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 753-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 754-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 755-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 756-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 757-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 758-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 759-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 760-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 761-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 762-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 763-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 764-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 765-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 766-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 767-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 768-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 769-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 770-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 771-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 772-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 773-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 774-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 775-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 776-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 777-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 778-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 779-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 780-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 781-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 782-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 783-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 784-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 785-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 786-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 787-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 788-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 789-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 790-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 791-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 792-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 793-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 794-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 795-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 796-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 797-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 798-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 799-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 800-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 801-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 802-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 803-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 804-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 805-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 806-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 807-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 808-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 809-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 810-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 811-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 812-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 813-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 814-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 815-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 816-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 817-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 818-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 819-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 820-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 821-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 822-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 823-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 824-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 825-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 826-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 827-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 828-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 829-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 830-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 831-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 832-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 833-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 834-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 835-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 836-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 837-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 838-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 839-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 840-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 841-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 842-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 843-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 844-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