Učitavanje...
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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| Izdano u: | BMC Bioinformatics |
|---|---|
| Glavni autori: | , , , , , , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
BioMed Central
2020
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| Teme: | |
| Online pristup: | 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 |
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