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ABSTRACT: Background
Single-cell RNA-sequencing (scRNA) datasets are becoming increasingly popular in clinical and cohort studies, but there is a lack of methods to investigate differentially expressed (DE) genes among such datasets with numerous individuals. While numerous methods exist to find DE genes for scRNA data from limited individuals, differential-expression testing for large cohorts of case and control individuals using scRNA data poses unique challenges due to substantial effects of human variation, i.e., individual-level confounding covariates that are difficult to account for in the presence of sparsely-observed genes.Results
We develop the eSVD-DE, a matrix factorization that pools information across genes and removes confounding covariate effects, followed by a novel
SUBMITTER: Lin KZ
PROVIDER: S-EPMC10690270 | biostudies-literature | 2024 Mar
REPOSITORIES: biostudies-literature