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McImpute: Matrix Completion Based Imputation for Single Cell RNA-seq Data
Motivation: Single-cell RNA sequencing has been proved to be revolutionary for its potential of zooming into complex biological systems. Genome-wide expression analysis at single-cell resolution provides a window into dynamics of cellular phenotypes. This facilitates the characterization of transcri...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6361810/ https://www.ncbi.nlm.nih.gov/pubmed/30761179 http://dx.doi.org/10.3389/fgene.2019.00009 |
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author | Mongia, Aanchal Sengupta, Debarka Majumdar, Angshul |
author_facet | Mongia, Aanchal Sengupta, Debarka Majumdar, Angshul |
author_sort | Mongia, Aanchal |
collection | PubMed |
description | Motivation: Single-cell RNA sequencing has been proved to be revolutionary for its potential of zooming into complex biological systems. Genome-wide expression analysis at single-cell resolution provides a window into dynamics of cellular phenotypes. This facilitates the characterization of transcriptional heterogeneity in normal and diseased tissues under various conditions. It also sheds light on the development or emergence of specific cell populations and phenotypes. However, owing to the paucity of input RNA, a typical single cell RNA sequencing data features a high number of dropout events where transcripts fail to get amplified. Results: We introduce mcImpute, a low-rank matrix completion based technique to impute dropouts in single cell expression data. On a number of real datasets, application of mcImpute yields significant improvements in the separation of true zeros from dropouts, cell-clustering, differential expression analysis, cell type separability, the performance of dimensionality reduction techniques for cell visualization, and gene distribution. Availability and Implementation: https://github.com/aanchalMongia/McImpute_scRNAseq |
format | Online Article Text |
id | pubmed-6361810 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-63618102019-02-13 McImpute: Matrix Completion Based Imputation for Single Cell RNA-seq Data Mongia, Aanchal Sengupta, Debarka Majumdar, Angshul Front Genet Genetics Motivation: Single-cell RNA sequencing has been proved to be revolutionary for its potential of zooming into complex biological systems. Genome-wide expression analysis at single-cell resolution provides a window into dynamics of cellular phenotypes. This facilitates the characterization of transcriptional heterogeneity in normal and diseased tissues under various conditions. It also sheds light on the development or emergence of specific cell populations and phenotypes. However, owing to the paucity of input RNA, a typical single cell RNA sequencing data features a high number of dropout events where transcripts fail to get amplified. Results: We introduce mcImpute, a low-rank matrix completion based technique to impute dropouts in single cell expression data. On a number of real datasets, application of mcImpute yields significant improvements in the separation of true zeros from dropouts, cell-clustering, differential expression analysis, cell type separability, the performance of dimensionality reduction techniques for cell visualization, and gene distribution. Availability and Implementation: https://github.com/aanchalMongia/McImpute_scRNAseq Frontiers Media S.A. 2019-01-29 /pmc/articles/PMC6361810/ /pubmed/30761179 http://dx.doi.org/10.3389/fgene.2019.00009 Text en Copyright © 2019 Mongia, Sengupta and Majumdar. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Genetics Mongia, Aanchal Sengupta, Debarka Majumdar, Angshul McImpute: Matrix Completion Based Imputation for Single Cell RNA-seq Data |
title | McImpute: Matrix Completion Based Imputation for Single Cell RNA-seq Data |
title_full | McImpute: Matrix Completion Based Imputation for Single Cell RNA-seq Data |
title_fullStr | McImpute: Matrix Completion Based Imputation for Single Cell RNA-seq Data |
title_full_unstemmed | McImpute: Matrix Completion Based Imputation for Single Cell RNA-seq Data |
title_short | McImpute: Matrix Completion Based Imputation for Single Cell RNA-seq Data |
title_sort | mcimpute: matrix completion based imputation for single cell rna-seq data |
topic | Genetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6361810/ https://www.ncbi.nlm.nih.gov/pubmed/30761179 http://dx.doi.org/10.3389/fgene.2019.00009 |
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