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Gene-based comparative analysis of tools for estimating copy number alterations using whole-exome sequencing data
Accurate detection of copy number alterations (CNAs) using next-generation sequencing technology is essential for the development and application of more precise medical treatments for human cancer. Here, we evaluated seven CNA estimation tools (ExomeCNV, CoNIFER, VarScan2, CODEX, ngCGH, saasCNV, an...
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| Pubblicato in: | Oncotarget |
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| Autori principali: | , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Impact Journals LLC
2017
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5432334/ https://ncbi.nlm.nih.gov/pubmed/28460482 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.18632/oncotarget.15932 |
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