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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...
שמור ב:
| הוצא לאור ב: | PLoS One |
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| Main Authors: | , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Public Library of Science
2018
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5933770/ https://ncbi.nlm.nih.gov/pubmed/29723276 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0196849 |
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