Major
Bioinformatics
Anticipated Graduation Year
2021
Access Type
Open Access
Abstract
The central dogma of biology describes how an individual's genome contributes to their unique phenotypes: genes encoded in DNA get transcribed into mRNA molecules, which get translated into proteins. Nevertheless, the path from genotype to phenotype is not straightforward, and unraveling the specific molecular mechanisms by which a genotype results in a phenotype is particularly challenging. Multi-omics approaches seek to combat this issue by integrating a variety of omics data into genetic analyses. The combination of genome-wide association studies, which calculate associations between SNPs and traits, transcriptome-wide association studies, which calculate associations between transcripts and traits, and expression quantitative trait loci, which identify SNPs associated with varying expression levels, can help further elucidate causative variants with respect to a phenotype. This project aims at bringing another omics relationship into the fold - associations between transcripts and protein levels by performing TWAS for proteins using protein level data from individuals in the Trans-Omics for Precision Medicine cohort and predicted expression levels from the PrediXcan software, calculated with Genotype-Tissue Expression Project expression models.
Faculty Mentors & Instructors
Dr. Heather Wheeler, Loyola University Chicago Department of Biology
Creative Commons License
This work is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 License.
Determining the Genetic Component of Protein Levels Using TWAS
The central dogma of biology describes how an individual's genome contributes to their unique phenotypes: genes encoded in DNA get transcribed into mRNA molecules, which get translated into proteins. Nevertheless, the path from genotype to phenotype is not straightforward, and unraveling the specific molecular mechanisms by which a genotype results in a phenotype is particularly challenging. Multi-omics approaches seek to combat this issue by integrating a variety of omics data into genetic analyses. The combination of genome-wide association studies, which calculate associations between SNPs and traits, transcriptome-wide association studies, which calculate associations between transcripts and traits, and expression quantitative trait loci, which identify SNPs associated with varying expression levels, can help further elucidate causative variants with respect to a phenotype. This project aims at bringing another omics relationship into the fold - associations between transcripts and protein levels by performing TWAS for proteins using protein level data from individuals in the Trans-Omics for Precision Medicine cohort and predicted expression levels from the PrediXcan software, calculated with Genotype-Tissue Expression Project expression models.