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DeAnnCNV: a tool for online detection and annotation of copy number variations from whole-exome sequencing data
With the decrease in costs, whole-exome sequencing (WES) has become a very popular and powerful tool for the identification of genetic variants underlying human diseases. However, integrated tools to precisely detect and systematically annotate copy number variations (CNVs) from WES data are still i...
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| Vydáno v: | Nucleic Acids Res |
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| Hlavní autoři: | , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Oxford University Press
2015
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4489280/ https://ncbi.nlm.nih.gov/pubmed/26013811 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gkv556 |
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