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The human gene damage index as a gene-level approach to prioritizing exome variants
The protein-coding exome of a patient with a monogenic disease contains about 20,000 variants, only one or two of which are disease causing. We found that 58% of rare variants in the protein-coding exome of the general population are located in only 2% of the genes. Prompted by this observation, we...
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Foilsithe in: | Proc Natl Acad Sci U S A |
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Main Authors: | , , , , , , , , , , , , , , , , , , , , , , , , , |
Formáid: | Artigo |
Teanga: | Inglês |
Foilsithe: |
National Academy of Sciences
2015
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Ábhair: | |
Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4640721/ https://ncbi.nlm.nih.gov/pubmed/26483451 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1518646112 |
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