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M3Drop: dropout-based feature selection for scRNASeq
MOTIVATION: Most genomes contain thousands of genes, but for most functional responses, only a subset of those genes are relevant. To facilitate many single-cell RNASeq (scRNASeq) analyses the set of genes is often reduced through feature selection, i.e. by removing genes only subject to technical n...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6691329/ https://www.ncbi.nlm.nih.gov/pubmed/30590489 http://dx.doi.org/10.1093/bioinformatics/bty1044 |
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author | Andrews, Tallulah S Hemberg, Martin |
author_facet | Andrews, Tallulah S Hemberg, Martin |
author_sort | Andrews, Tallulah S |
collection | PubMed |
description | MOTIVATION: Most genomes contain thousands of genes, but for most functional responses, only a subset of those genes are relevant. To facilitate many single-cell RNASeq (scRNASeq) analyses the set of genes is often reduced through feature selection, i.e. by removing genes only subject to technical noise. RESULTS: We present M3Drop, an R package that implements popular existing feature selection methods and two novel methods which take advantage of the prevalence of zeros (dropouts) in scRNASeq data to identify features. We show these new methods outperform existing methods on simulated and real datasets. AVAILABILITY AND IMPLEMENTATION: M3Drop is freely available on github as an R package and is compatible with other popular scRNASeq tools: https://github.com/tallulandrews/M3Drop. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. |
format | Online Article Text |
id | pubmed-6691329 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-66913292019-08-16 M3Drop: dropout-based feature selection for scRNASeq Andrews, Tallulah S Hemberg, Martin Bioinformatics Applications Notes MOTIVATION: Most genomes contain thousands of genes, but for most functional responses, only a subset of those genes are relevant. To facilitate many single-cell RNASeq (scRNASeq) analyses the set of genes is often reduced through feature selection, i.e. by removing genes only subject to technical noise. RESULTS: We present M3Drop, an R package that implements popular existing feature selection methods and two novel methods which take advantage of the prevalence of zeros (dropouts) in scRNASeq data to identify features. We show these new methods outperform existing methods on simulated and real datasets. AVAILABILITY AND IMPLEMENTATION: M3Drop is freely available on github as an R package and is compatible with other popular scRNASeq tools: https://github.com/tallulandrews/M3Drop. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. Oxford University Press 2019-08-15 2018-12-24 /pmc/articles/PMC6691329/ /pubmed/30590489 http://dx.doi.org/10.1093/bioinformatics/bty1044 Text en © The Author(s) 2018. Published by Oxford University Press. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Applications Notes Andrews, Tallulah S Hemberg, Martin M3Drop: dropout-based feature selection for scRNASeq |
title | M3Drop: dropout-based feature selection for scRNASeq |
title_full | M3Drop: dropout-based feature selection for scRNASeq |
title_fullStr | M3Drop: dropout-based feature selection for scRNASeq |
title_full_unstemmed | M3Drop: dropout-based feature selection for scRNASeq |
title_short | M3Drop: dropout-based feature selection for scRNASeq |
title_sort | m3drop: dropout-based feature selection for scrnaseq |
topic | Applications Notes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6691329/ https://www.ncbi.nlm.nih.gov/pubmed/30590489 http://dx.doi.org/10.1093/bioinformatics/bty1044 |
work_keys_str_mv | AT andrewstallulahs m3dropdropoutbasedfeatureselectionforscrnaseq AT hembergmartin m3dropdropoutbasedfeatureselectionforscrnaseq |