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Methods for Collapsing Multiple Rare Variants in Whole-Genome Sequence Data
Genetic Analysis Workshop 18 provided whole-genome sequence data in a pedigree-based sample and longitudinal phenotype data for hypertension and related traits, presenting an excellent opportunity for evaluating analysis choices. We summarize the nine contributions to the working group on collapsing...
Gorde:
| Argitaratua izan da: | Genet Epidemiol |
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| Egile Nagusiak: | , , , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
2014
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4558905/ https://ncbi.nlm.nih.gov/pubmed/25112183 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/gepi.21820 |
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