When loss-of-function is loss of function: assessing mutational signatures and impact of loss-of-function genetic variants

MOTIVATION: Loss-of-function genetic variants are frequently associated with severe clinical phenotypes, yet many are present in the genomes of healthy individuals. The available methods to assess the impact of these variants rely primarily upon evolutionary conservation with little to no considerat...

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Detalles Bibliográficos
Autores principales: Pagel, Kymberleigh A, Pejaver, Vikas, Lin, Guan Ning, Nam, Hyun-Jun, Mort, Matthew, Cooper, David N, Sebat, Jonathan, Iakoucheva, Lilia M, Mooney, Sean D, Radivojac, Predrag
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Ismb/Eccb 2017: The 25th Annual Conference Intelligent Systems for Molecular Biology Held Jointly with the 16th Annual European Conference on Computational Biology, Prague, Czech Republic, July 21–25, 2017
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5870554/
https://www.ncbi.nlm.nih.gov/pubmed/28882004
http://dx.doi.org/10.1093/bioinformatics/btx272

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5870554/
https://www.ncbi.nlm.nih.gov/pubmed/28882004
http://dx.doi.org/10.1093/bioinformatics/btx272

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