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ABSTRACT: Motivation
Single-cell RNA-sequencing (scRNA-seq) has enabled the molecular profiling of thousands to millions of cells simultaneously in biologically heterogenous samples. Currently, the common practice in scRNA-seq is to determine cell type labels through unsupervised clustering and the examination of cluster-specific genes. However, even small differences in analysis and parameter choosing can greatly alter clustering results and thus impose great influence on which cell types are identified. Existing methods largely focus on determining the optimal number of robust clusters, which can be problematic for identifying cells of extremely low abundance due to their subtle contributions toward overall patterns of gene expression.Results
Here, we present a carefully designed f
SUBMITTER: Leary JR
PROVIDER: S-EPMC10412410 | biostudies-literature | 2023 Aug
REPOSITORIES: biostudies-literature