SDImpute

SDImpute is a statistical software tool specifically designed to address one of the main challenges in single-cell RNA sequencing (scRNA-seq) data analysis: the presence of dropouts. Dropouts, or missing data points, occur frequently in scRNA-seq datasets due to the low amount of mRNA extracted from each cell, leading to false zeros in gene expression measurements. These dropouts can significantly impair downstream analysis, such as clustering, visualization, and differential gene expression analysis, by obscuring the true heterogeneity and complexity of cell types in the sample.

SDImpute tackles this issue through a process called block imputation. The method intelligently identifies dropout events by analyzing gene expression levels and the variability of these expressions across similar cells and genes. Once dropouts are identified, SDImpute performs imputation by leveraging gene expression data from similar cells unaffected by dropouts. This approach allows for the recovery of missing data in a way that maintains the inherent heterogeneity of gene expression across different cells.

Topic

RNA-Seq;Gene transcripts;Gene expression;Cell biology

Detail

  • Operation: Imputation;Differential gene expression profiling;Visualisation;Principal component analysis;Essential dynamics

  • Software interface: Library,Command-line tool

  • Language: R

  • License: The GNU General Public License v3.0

  • Cost: Free with restrictions

  • Version name: -

  • Credit: National Natural Science Foundation of China.

  • Input: -

  • Output: -

  • Contact: Jing Qi jinsl@hit.edu.cn

  • Collection: -

  • Maturity: -

Publications

  • SDImpute: A statistical block imputation method based on cell-level and gene-level information for dropouts in single-cell RNA-seq data.
  • Qi J, et al. SDImpute: A statistical block imputation method based on cell-level and gene-level information for dropouts in single-cell RNA-seq data. SDImpute: A statistical block imputation method based on cell-level and gene-level information for dropouts in single-cell RNA-seq data. 2021; 17:e1009118. doi: 10.1371/journal.pcbi.1009118
  • https://doi.org/10.1371/JOURNAL.PCBI.1009118
  • PMID: 34138847
  • PMC: PMC8266063

Download and documentation


< Back to DB search