Assessing the impact of mutations found in next generation sequencing data over human signaling pathways

Modern sequencing technologies produce increasingly detailed data on genomic variation. However, conventional methods for relating either individual variants or mutated genes to phenotypes present known limitations given the complex, multigenic nature of many diseases or traits. Here we present PATH...

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Detalles Bibliográficos
Autores principales: Hernansaiz-Ballesteros, Rosa D., Salavert, Francisco, Sebastián-León, Patricia, Alemán, Alejandro, Medina, Ignacio, Dopazo, Joaquín
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Web Server issue
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4489259/
https://www.ncbi.nlm.nih.gov/pubmed/25883139
http://dx.doi.org/10.1093/nar/gkv349

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4489259/
https://www.ncbi.nlm.nih.gov/pubmed/25883139
http://dx.doi.org/10.1093/nar/gkv349

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