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Collective judgment predicts disease-associated single nucleotide variants
BACKGROUND: In recent years the number of human genetic variants deposited into the publicly available databases has been increasing exponentially. The latest version of dbSNP, for example, contains ~50 million validated Single Nucleotide Variants (SNVs). SNVs make up most of human variation and are...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2013
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3839641/ https://www.ncbi.nlm.nih.gov/pubmed/23819846 http://dx.doi.org/10.1186/1471-2164-14-S3-S2 |