Principled "convergence" non-coding rare variant association testing in complex disease

Although many genetic loci pertinent to complex diseases have been identified and despite the fact that complex diseases remain an immense burden to healthcare globally, many details about the mechanism of these diseases are still unknown. Thus far, genome-wide association studies (GWAS) have only explained a small proportion of disease heritability, indicating that there is a large number of additional loci that contribute to complex diseases like type 2 diabetes (T2D), which is the primary case study in this work. We overcome some of the limitations of rare variant studies by conducting weighted aggregate association tests in a framework we call "Convergence". We compare potential cell type specific regulatory loci assigned to genes, which serve as the basis for grouping variants and integrated predictors of functional consequence of variants, which serve as variant weights. We demonstrate that this methodology is able to detect significant association to T2D for genes relevant for body weight homeostasis, adipocyte proliferation, and inflammation. As a result, this work provides a principled framework for improving the efficacy of RVAS by successfully converging the abundant epigenetic information available to understand complex disease.

Department dc:contributor.department

Massachusetts Institute of Technology. Department of Electrical Engineering and Computer Science

Grantor dc:publisher

Massachusetts Institute of Technology

Year dc:date.issued

2017

Author dc:creator

• Sosa, Daniel N.

Advisor dc:contributor.advisor

• Manolis Kellis.

• Electrical Engineering and Computer Science.

Statement dc:rights

• MIT theses are protected by copyright. They may be viewed, downloaded, or printed from this source but further reproduction or distribution in any format is prohibited without written permission.

Licence dc:rights.uri

• http://dspace.mit.edu/handle/1721.1/7582

Language dc:language.iso

eng

Handle dc:identifier.uri

http://hdl.handle.net/1721.1/113171

OAI identifier oai:identifier

oai:dspace.mit.edu:1721.1/113171