Decoding Brain Somatic Mosaicism with New Single-Cell Copy Number Analysis Methods
Name
zhao-zyf-phd-hst-2025-thesis.pdf
Description
Thesis PDF
Size
72.82 MB
Format
Adobe PDF
Checksum (MD5)
0b13ac63ffb18f9a2c7a20d76da54233
Author(s)
Zhao, Yifan
Advisor(s)
Park, Peter J.
Date Issued
May 2025
Publisher
Massachusetts Institute of Technology
Abstract
Copy number variants (CNVs) represent a significant but understudied form of somatic variation in the human brain, with potential implications for neurodevelopment, aging and disease. While single-cell whole-genome sequencing (scWGS) enables genome-wide profiling at single-cell resolution, existing computational methods struggle to accurately detect non-clonal CNVs, limiting our understanding of genomic mosaicism in the brain. In this thesis, I present two novel and complementary computational approaches for high-resolution CNV analysis in single cells. The first, HiScanner, is a CNV detection method that integrates single-cell assay-specific characteristics and introduces innovations in bin size optimization, read depth normalization, and joint segmentation across cells. Through extensive benchmarking experiments, I demonstrate HiScanner’s superior performance compared to existing tools. The second is a validation method that leverages unique molecular patterns from tagmentation-based scWGS, representing the first tool that exploits fragment overlap patterns to corroborate CNV predictions. I then apply these tools to investigate CNVs in three biological contexts: tumor evolution in paired initial and recurrent meningiomas, age-related genomic changes in neurotypical human brains, and developmental patterns in fetal and postnatal brain tissues. By analyzing both scWGS and multimodal single-cell data (paired RNA-seq and ATAC-seq), I characterize cell-type-specific CNV patterns and their potential functional implications. This work establishes a robust framework for studying somatic CNVs at single-cell resolution and provides insights into genomic instability in brain development, aging, and disease.
MIT Department
Harvard-MIT Program in Health Sciences and Technology
Terms of Use
In Copyright - Educational Use Permitted
Copyright retained by author(s)
Persistent DSpace Link