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VaRank: a simple and powerful tool for ranking genetic variants
Background. Most genetic disorders are caused by single nucleotide variations (SNVs) or small insertion/deletions (indels). High throughput sequencing has broadened the catalogue of human variation, including common polymorphisms, rare variations or disease causing mutations. However, identifying on...
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| Publicado en: | PeerJ |
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| Main Authors: | , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
PeerJ Inc.
2015
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4358652/ https://ncbi.nlm.nih.gov/pubmed/25780760 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7717/peerj.796 |
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