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Inferring rare disease risk variants based on exact probabilities of sharing by multiple affected relatives
Motivation: Family-based designs are regaining popularity for genomic sequencing studies because they provide a way to test cosegregation with disease of variants that are too rare in the population to be tested individually in a conventional case–control study. Results: Where only a few affected su...
Gorde:
| Egile Nagusiak: | , , , , , , , , , |
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| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
Oxford University Press
2014
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4103601/ https://ncbi.nlm.nih.gov/pubmed/24740360 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btu198 |
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