scPred

scPred classifies cells from single-cell RNA sequencing (scRNA-seq) data by extracting informative principal components via singular value decomposition and applying machine learning to identify cell-type transcriptional signatures.


Key Features:

  • Variance Structure Decomposition: Uses singular value decomposition and principal component analysis to identify principal components that capture variance informative of cell type and reduce dimensionality.
  • Unbiased Feature Selection: Selects features from the reduced-dimension space to retain only the most relevant components for classification.
  • Machine Learning Classification: Trains probability-based machine learning models on selected principal components to predict cell types.
  • Generalizability Across Datasets: Applies the same variance-driven dimensionality reduction and classifier framework across diverse scRNA-seq datasets and biological contexts.

Scientific Applications:

  • Cell Type Identification: Classifies individual cells by transcriptional profile to characterize specific cell types within complex tissues.
  • Transcriptional Signature Analysis: Identifies defining transcriptional signatures for studies of cellular differentiation and state transitions.
  • Cross-tissue and Condition Studies: Applied to diverse datasets including pancreatic tissue, mononuclear cells, colorectal tumor biopsies, and circulating dendritic cells.

Methodology:

Data preprocessing; variance-structure decomposition via singular value decomposition/principal component analysis; unbiased feature selection from the reduced-dimension space; machine learning model training on selected PCs; probability-based prediction and classification of cells in new datasets.

Topics

Details

License:
MIT
Programming Languages:
R
Added:
1/14/2020
Last Updated:
11/5/2024

Operations

Publications

Alquicira-Hernandez J, Sathe A, Ji HP, Nguyen Q, Powell JE. scPred: accurate supervised method for cell-type classification from single-cell RNA-seq data. Genome Biology. 2019;20(1). doi:10.1186/s13059-019-1862-5. PMID:31829268. PMCID:PMC6907144.