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The admixture maximum likelihood test to test for association between rare variants and disease phenotypes
BACKGROUND: The development of genotyping arrays containing hundreds of thousands of rare variants across the genome and advances in high-throughput sequencing technologies have made feasible empirical genetic association studies to search for rare disease susceptibility alleles. As single variant t...
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| Main Authors: | , , , |
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| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
BioMed Central
2013
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3698090/ https://ncbi.nlm.nih.gov/pubmed/23738568 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2105-14-177 |
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