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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...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | Bioinformatics |
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| Κύριοι συγγραφείς: | , , , , , , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
Oxford University Press
2017
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5870554/ https://ncbi.nlm.nih.gov/pubmed/28882004 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btx272 |
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