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VarAFT: a variant annotation and filtration system for human next generation sequencing data
With the rapidly developing high-throughput sequencing technologies known as next generation sequencing or NGS, our approach to gene hunting and diagnosis has drastically changed. In <10 years, these technologies have moved from gene panel to whole genome sequencing and from an exclusively resear...
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| Foilsithe in: | Nucleic Acids Res |
|---|---|
| Main Authors: | , , , , , , |
| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
Oxford University Press
2018
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6030844/ https://ncbi.nlm.nih.gov/pubmed/29860484 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gky471 |
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