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ASAP: a web-based platform for the analysis and interactive visualization of single-cell RNA-seq data

MOTIVATION: Single-cell RNA-sequencing (scRNA-seq) allows whole transcriptome profiling of thousands of individual cells, enabling the molecular exploration of tissues at the cellular level. Such analytical capacity is of great interest to many research groups in the world, yet these groups often la...

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Autores principales: Gardeux, Vincent, David, Fabrice P A, Shajkofci, Adrian, Schwalie, Petra C, Deplancke, Bart
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5870842/
https://www.ncbi.nlm.nih.gov/pubmed/28541377
http://dx.doi.org/10.1093/bioinformatics/btx337
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author Gardeux, Vincent
David, Fabrice P A
Shajkofci, Adrian
Schwalie, Petra C
Deplancke, Bart
author_facet Gardeux, Vincent
David, Fabrice P A
Shajkofci, Adrian
Schwalie, Petra C
Deplancke, Bart
author_sort Gardeux, Vincent
collection PubMed
description MOTIVATION: Single-cell RNA-sequencing (scRNA-seq) allows whole transcriptome profiling of thousands of individual cells, enabling the molecular exploration of tissues at the cellular level. Such analytical capacity is of great interest to many research groups in the world, yet these groups often lack the expertise to handle complex scRNA-seq datasets. RESULTS: We developed a fully integrated, web-based platform aimed at the complete analysis of scRNA-seq data post genome alignment: from the parsing, filtering and normalization of the input count data files, to the visual representation of the data, identification of cell clusters, differentially expressed genes (including cluster-specific marker genes), and functional gene set enrichment. This Automated Single-cell Analysis Pipeline (ASAP) combines a wide range of commonly used algorithms with sophisticated visualization tools. Compared with existing scRNA-seq analysis platforms, researchers (including those lacking computational expertise) are able to interact with the data in a straightforward fashion and in real time. Furthermore, given the overlap between scRNA-seq and bulk RNA-seq analysis workflows, ASAP should conceptually be broadly applicable to any RNA-seq dataset. As a validation, we demonstrate how we can use ASAP to simply reproduce the results from a single-cell study of 91 mouse cells involving five distinct cell types. AVAILABILITY AND IMPLEMENTATION: The tool is freely available at asap.epfl.ch and R/Python scripts are available at github.com/DeplanckeLab/ASAP. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
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spelling pubmed-58708422018-03-29 ASAP: a web-based platform for the analysis and interactive visualization of single-cell RNA-seq data Gardeux, Vincent David, Fabrice P A Shajkofci, Adrian Schwalie, Petra C Deplancke, Bart Bioinformatics Applications Notes MOTIVATION: Single-cell RNA-sequencing (scRNA-seq) allows whole transcriptome profiling of thousands of individual cells, enabling the molecular exploration of tissues at the cellular level. Such analytical capacity is of great interest to many research groups in the world, yet these groups often lack the expertise to handle complex scRNA-seq datasets. RESULTS: We developed a fully integrated, web-based platform aimed at the complete analysis of scRNA-seq data post genome alignment: from the parsing, filtering and normalization of the input count data files, to the visual representation of the data, identification of cell clusters, differentially expressed genes (including cluster-specific marker genes), and functional gene set enrichment. This Automated Single-cell Analysis Pipeline (ASAP) combines a wide range of commonly used algorithms with sophisticated visualization tools. Compared with existing scRNA-seq analysis platforms, researchers (including those lacking computational expertise) are able to interact with the data in a straightforward fashion and in real time. Furthermore, given the overlap between scRNA-seq and bulk RNA-seq analysis workflows, ASAP should conceptually be broadly applicable to any RNA-seq dataset. As a validation, we demonstrate how we can use ASAP to simply reproduce the results from a single-cell study of 91 mouse cells involving five distinct cell types. AVAILABILITY AND IMPLEMENTATION: The tool is freely available at asap.epfl.ch and R/Python scripts are available at github.com/DeplanckeLab/ASAP. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. Oxford University Press 2017-10-01 2017-05-24 /pmc/articles/PMC5870842/ /pubmed/28541377 http://dx.doi.org/10.1093/bioinformatics/btx337 Text en © The Author 2017. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Applications Notes
Gardeux, Vincent
David, Fabrice P A
Shajkofci, Adrian
Schwalie, Petra C
Deplancke, Bart
ASAP: a web-based platform for the analysis and interactive visualization of single-cell RNA-seq data
title ASAP: a web-based platform for the analysis and interactive visualization of single-cell RNA-seq data
title_full ASAP: a web-based platform for the analysis and interactive visualization of single-cell RNA-seq data
title_fullStr ASAP: a web-based platform for the analysis and interactive visualization of single-cell RNA-seq data
title_full_unstemmed ASAP: a web-based platform for the analysis and interactive visualization of single-cell RNA-seq data
title_short ASAP: a web-based platform for the analysis and interactive visualization of single-cell RNA-seq data
title_sort asap: a web-based platform for the analysis and interactive visualization of single-cell rna-seq data
topic Applications Notes
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5870842/
https://www.ncbi.nlm.nih.gov/pubmed/28541377
http://dx.doi.org/10.1093/bioinformatics/btx337
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