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CoNVEX: copy number variation estimation in exome sequencing data using HMM
BACKGROUND: One of the main types of genetic variations in cancer is Copy Number Variations (CNV). Whole exome sequenicng (WES) is a popular alternative to whole genome sequencing (WGS) to study disease specific genomic variations. However, finding CNV in Cancer samples using WES data has not been f...
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| Glavni autori: | , , |
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| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
BioMed Central
2013
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3549847/ https://ncbi.nlm.nih.gov/pubmed/23368785 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2105-14-S2-S2 |
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