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CopywriteR: DNA copy number detection from off-target sequence data
Current methods for detection of copy number variants (CNV) and aberrations (CNA) from targeted sequencing data are based on the depth of coverage of captured exons. Accurate CNA determination is complicated by uneven genomic distribution and non-uniform capture efficiency of targeted exons. Here we...
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| Publicado no: | Genome Biol |
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| Main Authors: | , , , , , , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4396974/ https://ncbi.nlm.nih.gov/pubmed/25887352 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13059-015-0617-1 |
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