The broad, long-term objective of this project concerns the development of novel statistical methods, theory and computational tools for statistical modeling of large-scale multiple high-dimensional genomic data motivated by important biological questions and experiments. New high-throughput technologies and next generation sequencing are generating various types of very high-dimensional genetics, genomic, epigenomics, metabolomics data in order to obtain an integrative understanding of various complex phenotypes. As the types and complexity of the data increase and as the questions being addressed become more sophisticated, statistical methods that can both integrate these genomic data and incorporate information about gene function and pathways are required in order to draw valid statistical and biological inferences.
The specific aims of the current project are to develop new statistical models and methods for causal integrative analysis of eQTL data with genome wide genetic association data (GWAS) in order to identify the possible causal genes and pathways for disease phenotypes. Motivated by analysis of diverse genomic data, the first aim is to develop novel causal mediation analysis methods to identify the genes that mediate the effects of genetic variants on disease phenotypes by constructing gene regulatory networks based on eQTL data.
Aim 2 is to develop high-dimensional instrumental variables (HDIV) regression models in order to identify the phenotype-causing genes using eQTLs as possible instrumental variables.
Aims 3 develops methods for estimating the genetic relatedness between disease phenotype and gene expressions in order to identify the possible disease causing genes and biological pathways. Finally, Aim 4 is to develop statistical methods that can effectively integrate GTEx data with GWAS association summary statistics in order to identify possible causal disease genes and pathways. These methods hinge on novel integration of methods for multiple related high-dimensional regressions and high-dimensional causal inference. The new methods can be applied to different types of genomic data and will ideally help facilitate the identification of genes and their complex interactions as well as the biological pathways underlying various complex human diseases. The work proposed here will contribute statistical methodology and theory for modeling high-dimensional genomic data and to studying complex phenotypes and biological systems and o er insights into each of the biological areas represented by the various data sets, including Alzheimer's disease, cardiometabolic syndrome, and chronic kidney disease. All algorithms and software tools developed under this grant and detailed documentation will be made available free-of-charge to interested researchers.

Public Health Relevance

and Relevance to Public Health This project aims to develop powerful statistical and computational methods for integrative analysis of diverse genomic data. The novel statistical methods are expected to gain more insights into how genomic perturbation and pathways dysfunction can lead to development of complex diseases such as Alzheimer's disease, cardiometabolic syndrome, and chronic kidney disease.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM129781-02
Application #
9752369
Study Section
Biostatistical Methods and Research Design Study Section (BMRD)
Program Officer
Brazhnik, Paul
Project Start
2018-09-01
Project End
2022-06-30
Budget Start
2019-07-01
Budget End
2020-06-30
Support Year
2
Fiscal Year
2019
Total Cost
Indirect Cost
Name
University of Pennsylvania
Department
Biostatistics & Other Math Sci
Type
Schools of Medicine
DUNS #
042250712
City
Philadelphia
State
PA
Country
United States
Zip Code
19104