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

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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Bibliographic Details
Main Authors: Junhua Rao, Lihua Peng, Xinming Liang, Hui Jiang, Chunyu Geng, Xia Zhao, Xin Liu, Guangyi Fan, Fang Chen, Feng Mu
Format: Article
Language:English
Published: BMC 2020-11-01
Series:BMC Bioinformatics
Subjects:
Copy number variant (CNV)
Whole-genome sequencing (WGS)
DNBSEQ
Benchmark
Online Access:http://link.springer.com/article/10.1186/s12859-020-03859-x

Internet

http://link.springer.com/article/10.1186/s12859-020-03859-x

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