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AluScanCNV2: An R package for copy number variation calling and cancer risk prediction with next-generation sequencing data
The usage of next-generation sequencing (NGS) to detect copy number variation (CNV) is widely accepted in cancer research. Based on an AluScanCNV software developed by us previously, an AluScanCNV2 software has been developed in the present study as an R package that performs CNV detection from NGS...
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| Yayımlandı: | Genes Dis |
|---|---|
| Asıl Yazarlar: | , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Chongqing Medical University
2018
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6411622/ https://ncbi.nlm.nih.gov/pubmed/30906832 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.gendis.2018.09.001 |
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