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...

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Detalles Bibliográficos
Autores principales: Rao, Junhua, Peng, Lihua, Liang, Xinming, Jiang, Hui, Geng, Chunyu, Zhao, Xia, Liu, Xin, Fan, Guangyi, Chen, Fang, Mu, Feng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7659224/
https://www.ncbi.nlm.nih.gov/pubmed/33176676
http://dx.doi.org/10.1186/s12859-020-03859-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7659224/
https://www.ncbi.nlm.nih.gov/pubmed/33176676
http://dx.doi.org/10.1186/s12859-020-03859-x

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