Performance of copy number variants detection based on whole-genome sequencing by DNBSEQ platforms

Abstract Background DNBSEQ™ platforms are new massively parallel sequencing (MPS) platforms that use DNA nanoball technology. Use of data generated from DNBSEQ™ platforms to detect single nucleotide variants (SNVs) and small insertions and deletions (indels) has proven to be quite effective, while t...

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Hlavní autoři:	Junhua Rao, Lihua Peng, Xinming Liang, Hui Jiang, Chunyu Geng, Xia Zhao, Xin Liu, Guangyi Fan, Fang Chen, Feng Mu
Médium:	Artigo
Jazyk:	Inglês
Vydáno:	BMC 2020-11-01
Edice:	BMC Bioinformatics
Témata:	Copy number variant (CNV) Whole-genome sequencing (WGS) DNBSEQ Benchmark
On-line přístup:	http://link.springer.com/article/10.1186/s12859-020-03859-x
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