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Joint Bayesian inference of risk variants and tissue-specific epigenomic enrichments across multiple complex human diseases

Genome wide association studies (GWAS) provide a powerful approach for uncovering disease-associated variants in human, but fine-mapping the causal variants remains a challenge. This is partly remedied by prioritization of disease-associated variants that overlap GWAS-enriched epigenomic annotations...

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Bibliografske podrobnosti
izdano v:Nucleic Acids Res
Main Authors: Li, Yue, Kellis, Manolis
Format: Artigo
Jezik:Inglês
Izdano: Oxford University Press 2016
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC5062982/
https://ncbi.nlm.nih.gov/pubmed/27407109
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gkw627
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