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DNA copy number profiling using single-cell sequencing
Currently, there is a lack of software for detecting copy number variations and constructing copy number profile for the whole genome from single-cell DNA sequencing data, which are often of low coverage and high technical noises. Here we introduce a new toolkit, SCNV, which features an efficient bi...
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| Publicado no: | Brief Bioinform |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6171490/ https://ncbi.nlm.nih.gov/pubmed/28159966 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bib/bbx004 |
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