CRAVAT: cancer-related analysis of variants toolkit

Summary: Advances in sequencing technology have greatly reduced the costs incurred in collecting raw sequencing data. Academic laboratories and researchers therefore now have access to very large datasets of genomic alterations but limited time and computational resources to analyse their potential...

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Detalles Bibliográficos
Autores principales: Douville, Christopher, Carter, Hannah, Kim, Rick, Niknafs, Noushin, Diekhans, Mark, Stenson, Peter D., Cooper, David N., Ryan, Michael, Karchin, Rachel
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/PMC3582272/
https://www.ncbi.nlm.nih.gov/pubmed/23325621
http://dx.doi.org/10.1093/bioinformatics/btt017

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3582272/
https://www.ncbi.nlm.nih.gov/pubmed/23325621
http://dx.doi.org/10.1093/bioinformatics/btt017

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