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Annotating pathogenic non-coding variants in genic regions
Identifying the underlying causes of disease requires accurate interpretation of genetic variants. Current methods ineffectively capture pathogenic non-coding variants in genic regions, resulting in overlooking synonymous and intronic variants when searching for disease risk. Here we present the Tra...
Uloženo v:
| Vydáno v: | Nat Commun |
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| Hlavní autoři: | , , , , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Nature Publishing Group UK
2017
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5550444/ https://ncbi.nlm.nih.gov/pubmed/28794409 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41467-017-00141-2 |
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