Cargando…
DrImpute: imputing dropout events in single cell RNA sequencing data
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...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5994079/ https://www.ncbi.nlm.nih.gov/pubmed/29884114 http://dx.doi.org/10.1186/s12859-018-2226-y |
_version_ | 1783330352519970816 |
---|---|
author | Gong, Wuming Kwak, Il-Youp Pota, Pruthvi Koyano-Nakagawa, Naoko Garry, Daniel J. |
author_facet | Gong, Wuming Kwak, Il-Youp Pota, Pruthvi Koyano-Nakagawa, Naoko Garry, Daniel J. |
author_sort | Gong, Wuming |
collection | PubMed |
description | 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. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12859-018-2226-y) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5994079 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-59940792018-06-21 DrImpute: imputing dropout events in single cell RNA sequencing data Gong, Wuming Kwak, Il-Youp Pota, Pruthvi Koyano-Nakagawa, Naoko Garry, Daniel J. BMC Bioinformatics Methodology Article 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. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12859-018-2226-y) contains supplementary material, which is available to authorized users. BioMed Central 2018-06-08 /pmc/articles/PMC5994079/ /pubmed/29884114 http://dx.doi.org/10.1186/s12859-018-2226-y Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Methodology Article Gong, Wuming Kwak, Il-Youp Pota, Pruthvi Koyano-Nakagawa, Naoko Garry, Daniel J. DrImpute: imputing dropout events in single cell RNA sequencing data |
title | DrImpute: imputing dropout events in single cell RNA sequencing data |
title_full | DrImpute: imputing dropout events in single cell RNA sequencing data |
title_fullStr | DrImpute: imputing dropout events in single cell RNA sequencing data |
title_full_unstemmed | DrImpute: imputing dropout events in single cell RNA sequencing data |
title_short | DrImpute: imputing dropout events in single cell RNA sequencing data |
title_sort | drimpute: imputing dropout events in single cell rna sequencing data |
topic | Methodology Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5994079/ https://www.ncbi.nlm.nih.gov/pubmed/29884114 http://dx.doi.org/10.1186/s12859-018-2226-y |
work_keys_str_mv | AT gongwuming drimputeimputingdropouteventsinsinglecellrnasequencingdata AT kwakilyoup drimputeimputingdropouteventsinsinglecellrnasequencingdata AT potapruthvi drimputeimputingdropouteventsinsinglecellrnasequencingdata AT koyanonakagawanaoko drimputeimputingdropouteventsinsinglecellrnasequencingdata AT garrydanielj drimputeimputingdropouteventsinsinglecellrnasequencingdata |