Efficient Methods for Imputation, Dimensionality Reduction, and Visualization of Single Cell RNA-Sequencing Data

NIH RePORTER · NIH · F30 · $50,520 · view on reporter.nih.gov ↗

Abstract

Project Summary: Efficient Methods for Imputation, Dimensionality Reduction, and Visualization of Single Cell RNA-Sequencing data Single cell RNA-sequencing (scRNA-seq) is revolutionizing the study of gene expression. In contrast to bulk RNA- sequencing, where the average expression of all cells in a sample is measured, scRNA-seq allows researchers to measure gene expression in each cell individually. This new technology has profound implications for both basic and clinical research but also presents unique analytic challenges. Among them is the problem of scale: scRNA- seq datasets are growing exponentially in size, with recently developed droplet-based technologies already profiling over 1 million cells in a single experiment. When applied to data of this scale, the most common methods for dimensionality reduction and visualization of scRNA-seq data, principal component analysis (PCA) and t-distributed Stochastic Neighborhood Embedding (t-SNE), require many hours of processing on servers with large amounts of memory. Furthermore, scRNA-seq technologies attempt to measure the extremely small amount of RNA in individual cells, resulting in a phenomenon called “dropout,” in which a gene is expressed but not detected and hence incorrectly measured as being unexpressed. In this fellowship, specifically tailored and highly scalable analysis methods for scRNA-seq data will be developed: 1) An ultra-fast, out-of-core implementation of randomized PCA allowing for anyone with a standard laptop to perform PCA of even the largest datasets. 2) An improved implementation of t-SNE that incorporates recent theoretical results and that will also use a numerical approximation called fast multipole methods to dramatically accelerate its runtime. 3) A method for imputing “dropped out” gene expression using recent results from the theory of low-rank matrix completion. In summary, this research will provide practical tools for analysis and visualization of scRNA-seq data. The fellowship also includes a training plan with valuable learning experiences for the applicant’s development as a physician-scientist who can apply computational and mathematical methods to solving biomedical problems.

Key facts

NIH application ID
9876960
Project number
5F30HG010102-03
Recipient
YALE UNIVERSITY
Principal Investigator
George Linderman
Activity code
F30
Funding institute
NIH
Fiscal year
2020
Award amount
$50,520
Award type
5
Project period
2018-03-01 → 2021-02-28