Cargando…
Detecting genome-wide directional effects of transcription factor binding on polygenic disease risk
Biological interpretation of GWAS data frequently involves assessing whether SNPs linked to a biological process, e.g., binding of a transcription factor (TF), show unsigned enrichment for disease signal. However, signed annotations quantifying whether each SNP allele promotes or hinders the biologi...
Autores principales: | Reshef, Yakir A, Finucane, Hilary K, Kelley, David R, Gusev, Alexander, Kotliar, Dylan, Ulirsch, Jacob C, Hormozdiari, Farhad, Nasser, Joseph, O’Connor, Luke, van de Geijn, Bryce, Loh, Po-Ru, Grossman, Sharon R, Bhatia, Gaurav, Gazal, Steven, Palamara, Pier Francesco, Pinello, Luca, Patterson, Nick, Adams, Ryan P, Price, Alkes L |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6202062/ https://www.ncbi.nlm.nih.gov/pubmed/30177862 http://dx.doi.org/10.1038/s41588-018-0196-7 |
Ejemplares similares
-
Functionally-informed fine-mapping and polygenic localization of complex trait heritability
por: Weissbrod, Omer, et al.
Publicado: (2020) -
Leveraging molecular quantitative trait loci to understand the genetic architecture of diseases and complex traits
por: Hormozdiari, Farhad, et al.
Publicado: (2018) -
Functional disease architectures reveal unique biological role of transposable elements
por: Hormozdiari, Farhad, et al.
Publicado: (2019) -
Evaluating the informativeness of deep learning annotations for human complex diseases
por: Dey, Kushal K., et al.
Publicado: (2020) -
Reference-based phasing using the Haplotype Reference Consortium panel
por: Loh, Po-Ru, et al.
Publicado: (2016)