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Reliable multiplex sequencing with rare index mis-assignment on DNB-based NGS platform
by
Chen, Ao
, Wang, Jingjing
, Mei, Zhiying
, Shen, Hanjie
, Xu, Xun
, Liu, Pengjuan
, Wei, Hanmin
, Liu, Jia Sophie
, Liang, Xinming
, Drmanac, Snezana
, Li, Qiaoling
, Du, Shiyi
, Yang, Huanming
, Wang, Jian
, Li, Li
, Jiang, Hui
, Zou, Jing
, Liu, Qiang
, Zhao, Xia
, Li, Zhanqing
, Drmanac, Radoje
, Zhang, Wenwei
, Xu, Dongyang
, Jiang, Yuan
, Wang, Xiaman
, Wang, Lin
, Zhang, Yongwei
in
Animal Genetics and Genomics
/ Biomedical and Life Sciences
/ Deoxyribonucleic acid
/ DNA
/ DNA biosynthesis
/ DNA nanoball technology
/ DNA sequencing
/ Gene sequencing
/ Genetic research
/ Genetic testing
/ Genomes
/ Genomics
/ Human and rodent genomics
/ Libraries
/ Life Sciences
/ Methods
/ Microarrays
/ Microbial Genetics and Genomics
/ Multiplex sequencing
/ Multiplexing
/ NGS
/ Nucleotide sequence
/ Plant Genetics and Genomics
/ Polymerase chain reaction
/ Proteomics
/ Quality control
/ Rare index mis-assignment
/ Research Article
/ Technology
/ Whole genome sequencing
2019
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Reliable multiplex sequencing with rare index mis-assignment on DNB-based NGS platform
by
Chen, Ao
, Wang, Jingjing
, Mei, Zhiying
, Shen, Hanjie
, Xu, Xun
, Liu, Pengjuan
, Wei, Hanmin
, Liu, Jia Sophie
, Liang, Xinming
, Drmanac, Snezana
, Li, Qiaoling
, Du, Shiyi
, Yang, Huanming
, Wang, Jian
, Li, Li
, Jiang, Hui
, Zou, Jing
, Liu, Qiang
, Zhao, Xia
, Li, Zhanqing
, Drmanac, Radoje
, Zhang, Wenwei
, Xu, Dongyang
, Jiang, Yuan
, Wang, Xiaman
, Wang, Lin
, Zhang, Yongwei
in
Animal Genetics and Genomics
/ Biomedical and Life Sciences
/ Deoxyribonucleic acid
/ DNA
/ DNA biosynthesis
/ DNA nanoball technology
/ DNA sequencing
/ Gene sequencing
/ Genetic research
/ Genetic testing
/ Genomes
/ Genomics
/ Human and rodent genomics
/ Libraries
/ Life Sciences
/ Methods
/ Microarrays
/ Microbial Genetics and Genomics
/ Multiplex sequencing
/ Multiplexing
/ NGS
/ Nucleotide sequence
/ Plant Genetics and Genomics
/ Polymerase chain reaction
/ Proteomics
/ Quality control
/ Rare index mis-assignment
/ Research Article
/ Technology
/ Whole genome sequencing
2019
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Reliable multiplex sequencing with rare index mis-assignment on DNB-based NGS platform
by
Chen, Ao
, Wang, Jingjing
, Mei, Zhiying
, Shen, Hanjie
, Xu, Xun
, Liu, Pengjuan
, Wei, Hanmin
, Liu, Jia Sophie
, Liang, Xinming
, Drmanac, Snezana
, Li, Qiaoling
, Du, Shiyi
, Yang, Huanming
, Wang, Jian
, Li, Li
, Jiang, Hui
, Zou, Jing
, Liu, Qiang
, Zhao, Xia
, Li, Zhanqing
, Drmanac, Radoje
, Zhang, Wenwei
, Xu, Dongyang
, Jiang, Yuan
, Wang, Xiaman
, Wang, Lin
, Zhang, Yongwei
in
Animal Genetics and Genomics
/ Biomedical and Life Sciences
/ Deoxyribonucleic acid
/ DNA
/ DNA biosynthesis
/ DNA nanoball technology
/ DNA sequencing
/ Gene sequencing
/ Genetic research
/ Genetic testing
/ Genomes
/ Genomics
/ Human and rodent genomics
/ Libraries
/ Life Sciences
/ Methods
/ Microarrays
/ Microbial Genetics and Genomics
/ Multiplex sequencing
/ Multiplexing
/ NGS
/ Nucleotide sequence
/ Plant Genetics and Genomics
/ Polymerase chain reaction
/ Proteomics
/ Quality control
/ Rare index mis-assignment
/ Research Article
/ Technology
/ Whole genome sequencing
2019
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Reliable multiplex sequencing with rare index mis-assignment on DNB-based NGS platform
Journal Article
Reliable multiplex sequencing with rare index mis-assignment on DNB-based NGS platform
2019
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Overview
Background
Massively-parallel-sequencing, coupled with sample multiplexing, has made genetic tests broadly affordable. However, intractable index mis-assignments (commonly exceeds 1%) were repeatedly reported on some widely used sequencing platforms.
Results
Here, we investigated this quality issue on BGI sequencers using three library preparation methods: whole genome sequencing (WGS) with PCR, PCR-free WGS, and two-step targeted PCR. BGI’s sequencers utilize a unique DNA nanoball (DNB) technology which uses rolling circle replication for DNA-nanoball preparation; this linear amplification is PCR free and can avoid error accumulation. We demonstrated that single index mis-assignment from free indexed oligos occurs at a rate of one in 36 million reads, suggesting virtually no index hopping during DNB creation and arraying. Furthermore, the DNB-based NGS libraries have achieved an unprecedentedly low sample-to-sample mis-assignment rate of 0.0001 to 0.0004% under recommended procedures.
Conclusions
Single indexing with DNB technology provides a simple but effective method for sensitive genetic assays with large sample numbers.
Publisher
BioMed Central,BioMed Central Ltd,Springer Nature B.V,BMC
Subject
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