HitWalker: variant prioritization for personalized functional cancer genomics

Summary: Determining the functional relevance of identified sequence variants in cancer is a prerequisite to ultimately matching specific therapies with individual patients. This level of mechanistic understanding requires integration of genomic information with complementary functional analyses to...

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Detalles Bibliográficos
Autores principales: Bottomly, Daniel, Wilmot, Beth, Tyner, Jeffrey W., Eide, Christopher A., Loriaux, Marc M., Druker, Brian J., McWeeney, Shannon K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2013
Materias:
Applications Notes
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3570211/
https://www.ncbi.nlm.nih.gov/pubmed/23303510
http://dx.doi.org/10.1093/bioinformatics/btt003

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3570211/
https://www.ncbi.nlm.nih.gov/pubmed/23303510
http://dx.doi.org/10.1093/bioinformatics/btt003

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