text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 980-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently 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 981-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 982-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 983-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 984-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 985-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 986-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 987-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 988-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 989-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 990-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 991-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 992-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 993-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 994-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 995-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 996-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and 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 997-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 998-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 999-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1000-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1001-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1002-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1003-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1004-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1005-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1006-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1007-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1008-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1009-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1010-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1011-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1012-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and 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 1013-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1014-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1015-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1016-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1017-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1018-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1019-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1020-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1021-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1022-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1023-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1024-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1025-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1026-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1027-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1028-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and 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 1029-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1030-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1031-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1032-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1033-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1034-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1035-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1036-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1037-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1038-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1039-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1040-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1041-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1042-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1043-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1044-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and 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 1045-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1046-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1047-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1048-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1049-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1050-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1051-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1052-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1053-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1054-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1055-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1056-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1057-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1058-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1059-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1060-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and 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 1061-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1062-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1063-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1064-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1065-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1066-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1067-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1068-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1069-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1070-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1071-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1072-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1073-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1074-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1075-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1076-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and 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 1077-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1078-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1079-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1080-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1081-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1082-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1083-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1084-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1085-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1086-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1087-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1088-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1089-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1090-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1091-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1092-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and 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 1093-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1094-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1095-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1096-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1097-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1098-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1099-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1100-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1101-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1102-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1103-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1104-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1105-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1106-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1107-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1108-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and 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 1109-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1110-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1111-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1112-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1113-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens


text: live

text: Human

text: Yifang Dai

text: Sequencing Library preparation was carried out in accordance with the manufacturer's instructions. In brief, total genomic DNA was extracted from tissue samples using the Amp Genomic DNA Kit (TIANGEN Biotech, Beijing, China). After shearing the genomic DNA to an average size of 200 bp, 2.5 ng of the fragmented DNA was used to create the sequencing library. End-repair and A-tailing was then perform, followed by the ligation of 1114-bp barcoded sequencing adaptors and treated DNA fragments. PCR was performed subsequently and the its product was purified using the magnetic beads.

text: Homo sapiens

text: female

text: chorionic villi

text: Human sample from Homo sapiens