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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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Bibliografiske detaljer
Udgivet i:Eur J Hum Genet
Hovedforfatter: Lin, Shili
Format: Artigo
Sprog:Inglês
Udgivet: Nature Publishing Group 2015
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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