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...

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Detalles Bibliográficos
Autores principales: Capriotti, Emidio, Altman, Russ B, Bromberg, Yana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Research
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

Internet

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

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