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

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 the feasi...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:BMC Bioinformatics
Prif Awduron: Rao, Junhua, Peng, Lihua, Liang, Xinming, Jiang, Hui, Geng, Chunyu, Zhao, Xia, Liu, Xin, Fan, Guangyi, Chen, Fang, Mu, Feng
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: BioMed Central 2020
Pynciau:
Research Article
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC7659224/
https://ncbi.nlm.nih.gov/pubmed/33176676
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-020-03859-x
Tagiau: Ychwanegu Tag
Dim Tagiau, Byddwch y cyntaf i dagio'r cofnod hwn!

Eitemau Tebyg