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MARV: a tool for genome-wide multi-phenotype analysis of rare variants
BACKGROUND: Genome-wide association studies have enabled identification of thousands of loci for hundreds of traits. Yet, for most human traits a substantial part of the estimated heritability is unexplained. This and recent advances in technology to produce high-dimensional data cost-effectively ha...
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| Publicado no: | BMC Bioinformatics |
|---|---|
| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5311849/ https://ncbi.nlm.nih.gov/pubmed/28209135 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-017-1530-2 |
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