Back to search

Article

Disease and phenotype relevant genetic variants identified from histone acetylomes in human hearts

2019-01-31

Abstract excerpt

Identifying genetic markers for heterogeneous complex diseases such as heart failure has been challenging, and may require prohibitively large cohort sizes in genome-wide association studies (GWAS) in order to demonstrate statistical significance 1 . On the other hand, chromatin quantitative trait loci (QTL), elucidated by direct epigenetic profiling of specific human tissues, may contribute towards prioritising...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work
f1d1151c-a3bc-5e4f-a56d-b53dda0e8c7c
DOI
10.1101/536763
Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest
Interactive article relationship graphSelect a related publication card to move it into the centre and load its closest explainable connections. Solid lines are source-backed structured connections. Dashed lines are semantic discovery signals and are not scientific evidence.
Disease and phenotype relevant genetic variants identified from histone acetylomes in human heartsDOI 10.1101/536763
Select a neighboring publication to make it the new centre.