VaRank: a simple and powerful tool for ranking genetic variants

Background. Most genetic disorders are caused by single nucleotide variations (SNVs) or small insertion/deletions (indels). High throughput sequencing has broadened the catalogue of human variation, including common polymorphisms, rare variations or disease causing mutations. However, identifying on...

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Detalles Bibliográficos
Autores principales: Geoffroy, Véronique, Pizot, Cécile, Redin, Claire, Piton, Amélie, Vasli, Nasim, Stoetzel, Corinne, Blavier, André, Laporte, Jocelyn, Muller, Jean
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2015
Materias:
Bioinformatics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4358652/
https://www.ncbi.nlm.nih.gov/pubmed/25780760
http://dx.doi.org/10.7717/peerj.796

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4358652/
https://www.ncbi.nlm.nih.gov/pubmed/25780760
http://dx.doi.org/10.7717/peerj.796

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