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FamLBL: detecting rare haplotype disease association based on common SNPs using case-parent triads
Motivation: In recent years, there has been an increasing interest in using common single-nucleotide polymorphisms (SNPs) amassed in genome-wide association studies to investigate rare haplotype effects on complex diseases. Evidence has suggested that rare haplotypes may tag rare causal single-nucle...
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| Hlavní autoři: | , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Oxford University Press
2014
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| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4155250/ https://ncbi.nlm.nih.gov/pubmed/24849576 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btu347 |
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