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GeneTalk: an expert exchange platform for assessing rare sequence variants in personal genomes
Summary: Next-generation sequencing has become a powerful tool in personalized medicine. Exomes or even whole genomes of patients suffering from rare diseases are screened for sequence variants. After filtering out common polymorphisms, the assessment and interpretation of detected personal variants...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Oxford University Press
2012
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3463119/ https://www.ncbi.nlm.nih.gov/pubmed/22826540 http://dx.doi.org/10.1093/bioinformatics/bts462 |