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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...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | Eur J Hum Genet |
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| Κύριος συγγραφέας: | |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
Nature Publishing Group
2015
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| Θέματα: | |
| Διαθέσιμο Online: | 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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