Načítá se...
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...
Uloženo v:
| Vydáno v: | Eur J Hum Genet |
|---|---|
| Hlavní autor: | |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Nature Publishing Group
2015
|
| Témata: | |
| On-line přístup: | 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 |
| Tagy: |
Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!
|