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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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| 出版年: | Genes Dis |
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| 主要な著者: | , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Chongqing Medical University
2018
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| 主題: | |
| オンライン･アクセス: | 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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