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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...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Public Library of Science
2018
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| Materias: | |
| 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 |