Back to results

Massachusetts Institute of Technology

Towards causality in gene regulatory network inference

Abstract

dc:description.abstract

Understanding the coordination of biomolecules that underlies gene regulation is key to gaining mechanistic insights into cellular functions, phenotypes, and diseases. Advances in single-cell technologies promise to unveil mechanisms of gene regulation at unprecedented resolution by enabling measurements of genomic and/or epigenetic features for individual cells. However, unlocking insights from single-cell data requires algorithmic innovations. This thesis introduces a series of methods for uncovering gene regulatory relationships underlying cellular identity and function from single-cell data. Firstly, we present a framework for enhancing the detection of statistical associations in small sample size settings for gene regulatory network inference. We then describe the use of single-cell genetic perturbation screens for determining the causal roles of critical regulatory complexes, focusing specifically on its applications for revealing mechanistic insights about the mammalian SWI/SNF family of chromatin remodeling complexes. To bridge the gap between methods that identify statistical associations from observational data and those that infer causal relationships using interventions, we also introduce a new category of techniques that extends the econometric concept of Granger causality to complex graph-based dynamical systems, such as those found in single-cell trajectories. In particular, we describe a graph neural network-based generalization of Granger causality for single-cell multimodal data that enables the detection of noncoding genomic loci implicated in the regulation of specific genes. We then demonstrate how we use this approach to link genetic variants to gene dysregulation in disease, focusing on its applications to schizophrenia etiology. Lastly, we present an extension of this graph-based Granger causal framework that leverages RNA velocity dynamics for causal gene regulatory network inference and enables inquiries into the role of temporal control in gene regulatory function and disease.

Degree

thesis:*
Name thesis:degree_name
Doctoral
Department dc:contributor.department
Massachusetts Institute of Technology. Computational and Systems Biology Program
Grantor dc:publisher
Massachusetts Institute of Technology
Year dc:date.issued
2023

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Wu, Alexander Po-Yen
Advisor dc:contributor.advisor
  • Berger, Bonnie A.

Rights

dc:rights
Statement dc:rights
  • In Copyright - Educational Use Permitted
  • Copyright retained by author(s)

Identifiers

dc:identifier.*
Handle dc:identifier.uri
https://hdl.handle.net/1721.1/151203
OAI identifier oai:identifier
oai:dspace.mit.edu:1721.1/151203

Chain of custody

source
Harvested from
MIT
Base URL
dspace.mit.edu/oai/request
Last updated
2026-07-22
Source record
OAI-PMH GetRecord
related terms
citation

Wu, Alexander Po-Yen. Towards causality in gene regulatory network inference. Massachusetts Institute of Technology, 2023. https://hdl.handle.net/1721.1/151203