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CanVar: A resource for sharing germline variation in cancer patients
The advent of high-throughput sequencing has accelerated our ability to discover genes predisposing to disease and is transforming clinical genomic sequencing. In both contexts knowledge of the spectrum and frequency of genetic variation in the general population and in disease cohorts is vital to t...
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| Publicado no: | F1000Res |
|---|---|
| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
F1000Research
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5200944/ https://ncbi.nlm.nih.gov/pubmed/28105316 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12688/f1000research.10058.1 |
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