Joint Analysis of Microbiome and Other Genomic Data Types

NIH RePORTER · NIH · R01 · $175,629 · view on reporter.nih.gov ↗

Abstract

PROJECT SUMMARY In the same way that the human genome project created invaluable genomic maps, the objective of this project is to develop methods for eventual construction of comprehensive genetic and metabolomic by microbome relationship maps. Such maps would be an invaluable resource for improving our understanding as to the underlying mechanisms by which microbes and –omics features influence human diseases and conditions, potentially leading to identification of novel therapeutic targets. To these ends, this proposal seeks to develop statistical and computational tools for mapping associations and interactions between microbes and other – omic features and for further utilizing other –omics to improve microbiome based prediction models. Specifically, motivated by studies examining the role of the vaginal microbiome and other –omics in birth outcomes and menopause, we aim to develop statistical methodology for (1) mapping genetic variants that influence microbiome composition so as to understand the innate component of the microbiome as well as learn mechanisms by which genetics influence outcomes; (2) creating global metabolic maps integrating both microbes and metabolites which will enable understanding of how perturbations might influence the system and identify key pathways for therapeutic target; (3) exploiting other –omics in constructing more accurate microbiome based prediction models for preterm birth; (4) developing, distributing and supporting software packages for the proposed methods. The methods are based on frameworks in which we have considerable experience, but novel technical contributions are made to accommodate features of the data such as population stratification and relatedness in genetics, phylogenetic structure, and compositionality, as well as practical considerations such as availability of samples and other –omics data. Consequently, these new methods have the potential for accelerating mechanistic and translational microbiome studies, developing vital resources for enabling systematic achievement of many biological, clinical, and public health problems that have eluded researchers for decades.

Key facts

NIH application ID
10172929
Project number
5R01GM129512-04
Recipient
FRED HUTCHINSON CANCER RESEARCH CENTER
Principal Investigator
MICHAEL Chiao-An WU
Activity code
R01
Funding institute
NIH
Fiscal year
2021
Award amount
$175,629
Award type
5
Project period
2018-09-01 → 2022-03-31