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A web-based interactive framework to assist in the prioritization of disease candidate genes in whole-exome sequencing studies
Whole-exome sequencing has become a fundamental tool for the discovery of disease-related genes of familial diseases and the identification of somatic driver variants in cancer. However, finding the causal mutation among the enormous background of individual variability in a small number of samples...
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Oxford University Press
2014
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4086071/ https://www.ncbi.nlm.nih.gov/pubmed/24803668 http://dx.doi.org/10.1093/nar/gku407 |