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Kullback–Leibler divergence for detection of rare haplotype common disease association
Rare haplotypes may tag rare causal variants of common diseases; hence, detection of such rare haplotypes may also contribute to our understanding of complex disease etiology. Because rare haplotypes frequently result from common single-nucleotide polymorphisms (SNPs), focusing on rare haplotypes is...
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| Udgivet i: | Eur J Hum Genet |
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| Hovedforfatter: | |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Nature Publishing Group
2015
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4613467/ https://ncbi.nlm.nih.gov/pubmed/25735482 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2015.25 |
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