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 845-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 846-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 847-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 848-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 849-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 850-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 851-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 852-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 853-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 854-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 855-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 856-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 857-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 858-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 859-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 860-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 861-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 862-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 863-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 864-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 865-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 866-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 867-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 868-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 869-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 870-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 871-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 872-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 873-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 874-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 875-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 876-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 877-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 878-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 879-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 880-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 881-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 882-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 883-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 884-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 885-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 886-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 887-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 888-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 889-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 890-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 891-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 892-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 893-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 894-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 895-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 896-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 897-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 898-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 899-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 900-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 901-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 902-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 903-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 904-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 905-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 906-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 907-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 908-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 909-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 910-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 911-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 912-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 913-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 914-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 915-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 916-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 917-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 918-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 919-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 920-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 921-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 922-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 923-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 924-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 925-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 926-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 927-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 928-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 929-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 930-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 931-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 932-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 933-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 934-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 935-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 936-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 937-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 938-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 939-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 940-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 941-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 942-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 943-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 944-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 945-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 946-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 947-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 948-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 949-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 950-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 951-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 952-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 953-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 954-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 955-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 956-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 957-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 958-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 959-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 960-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 961-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 962-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 963-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 964-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 965-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 966-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 967-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 968-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 969-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 970-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 971-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 972-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 973-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 974-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 975-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 976-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 977-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 978-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 979-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