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Tools for Predicting the Functional Impact of Nonsynonymous Genetic Variation
As personal genome sequencing becomes a reality, understanding the effects of genetic variants on phenotype—particularly the impact of germline variants on disease risk and the impact of somatic variants on cancer development and treatment—continues to increase in importance. Because of their clear...
Tallennettuna:
| Julkaisussa: | Genetics |
|---|---|
| Päätekijät: | , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Genetics Society of America
2016
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4896183/ https://ncbi.nlm.nih.gov/pubmed/27270698 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1534/genetics.116.190033 |
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