scLRTC

scLRTC applies low-rank tensor completion to impute dropout events in single-cell RNA sequencing (scRNA-seq) data, restoring gene–cell expression matrices and preserving gene-to-gene and cell-to-cell correlations for downstream analyses.


Key Features:

  • Imputation Accuracy: Imputes dropout entries and quantifies accuracy using sum of squared error (SSE) and Pearson correlation coefficient (PCC).
  • Performance on Simulated Datasets: Outperforms other state-of-the-art methods on simulated scRNA-seq datasets in imputation fidelity.
  • Effectiveness on Real Datasets: Improves cell classification on real scRNA-seq datasets across clustering approaches such as SC3 or t-SNE followed by K-means, evaluated by adjusted rand index (ARI) and normalized mutual information (NMI).
  • Correlation Preservation: Restores both gene-to-gene and cell-to-cell correlations through reconstruction of expression values.
  • Versatility in Applications: Supports downstream tasks including cell visualization and inference of cell lineage trajectories.

Scientific Applications:

  • Cell Type Clustering: Provides an imputed expression matrix as input for cell type clustering analyses.
  • Dimension Reduction and Visualization: Reduces dropout-induced noise to improve dimension reduction and visualization methods such as t-SNE.
  • Cell Lineage Trajectory Inference: Supplies denoised expression data for inferring cell lineage trajectories.

Methodology:

Constructs a third-order low-rank tensor leveraging similarities among single cells, applies tensor decomposition to denoise the data, and uses a low-rank tensor completion algorithm to reconstruct cell expression levels.

Topics

Details

License:
Not licensed
Cost:
Free of charge
Tool Type:
library
Operating Systems:
Mac, Linux, Windows
Programming Languages:
MATLAB, R, Python
Added:
1/28/2022
Last Updated:
1/28/2022

Operations

Data Inputs & Outputs

Publications

Pan X, Li Z, Qin S, Yu M, Hu H. ScLRTC: imputation for single-cell RNA-seq data via low-rank tensor completion. BMC Genomics. 2021;22(1). doi:10.1186/s12864-021-08101-3. PMID:34844559. PMCID:PMC8628418.