DrImpute: imputing dropout events in single cell RNA sequencing data.

BMC Bioinformatics

Lillehei Heart Institute, University of Minnesota, 2231 6th St S.E, 4-165 CCRB, Minneapolis, MN, 55114, USA.

Published: June 2018

AI Article Synopsis

  • scRNA-seq allows researchers to study gene expression at the single cell level, but it faces challenges due to technical and biological noise, including dropout events where true gene expressions are missed.
  • DrImpute is a newly developed tool designed to impute (fill in) these dropout events, proving to be more effective than other existing algorithms in differentiating between dropout zeros and actual zeros.
  • By enhancing data analysis, DrImpute improves clustering, visualization, and lineage reconstruction across multiple datasets and is available for use on R at its GitHub page.

Article Abstract

Background: The single cell RNA sequencing (scRNA-seq) technique begin a new era by allowing the observation of gene expression at the single cell level. However, there is also a large amount of technical and biological noise. Because of the low number of RNA transcriptomes and the stochastic nature of the gene expression pattern, there is a high chance of missing nonzero entries as zero, which are called dropout events.

Results: We develop DrImpute to impute dropout events in scRNA-seq data. We show that DrImpute has significantly better performance on the separation of the dropout zeros from true zeros than existing imputation algorithms. We also demonstrate that DrImpute can significantly improve the performance of existing tools for clustering, visualization and lineage reconstruction of nine published scRNA-seq datasets.

Conclusions: DrImpute can serve as a very useful addition to the currently existing statistical tools for single cell RNA-seq analysis. DrImpute is implemented in R and is available at https://github.com/gongx030/DrImpute .

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5994079PMC
http://dx.doi.org/10.1186/s12859-018-2226-yDOI Listing

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