ENTPRISE-X: Predicting disease-associated frameshift and nonsense mutations

To exploit the plethora of information provided by Next Generation Sequencing, the identification of the genetic mutations responsible for disease in general or cancer in particular, among the thousands of neutral germline or somatic variations is a crucial task. Genome-wide association studies for...

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Detalles Bibliográficos
Autores principales: Zhou, Hongyi, Gao, Mu, Skolnick, Jeffrey
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5933770/
https://www.ncbi.nlm.nih.gov/pubmed/29723276
http://dx.doi.org/10.1371/journal.pone.0196849

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5933770/
https://www.ncbi.nlm.nih.gov/pubmed/29723276
http://dx.doi.org/10.1371/journal.pone.0196849

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