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wANNOVAR: annotating genetic variants for personal genomes via the web
BACKGROUND: High-throughput DNA sequencing platforms have become widely available. As a result, personal genomes are increasingly being sequenced in research and clinical settings. However, the resulting massive amounts of variants data pose significant challenges to the average biologists and clini...
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| Main Authors: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2012
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3556337/ https://ncbi.nlm.nih.gov/pubmed/22717648 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmedgenet-2012-100918 |
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