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Exome sequencing-based copy-number variation and loss of heterozygosity detection: ExomeCNV
Motivation: The ability to detect copy-number variation (CNV) and loss of heterozygosity (LOH) from exome sequencing data extends the utility of this powerful approach that has mainly been used for point or small insertion/deletion detection. Results: We present ExomeCNV, a statistical method to det...
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| Asıl Yazarlar: | , , , , , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Oxford University Press
2011
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3179661/ https://ncbi.nlm.nih.gov/pubmed/21828086 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btr462 |
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