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Meta-analysis of crowdsourced data compendia suggests pan-disease transcriptional signatures of autoimmunity
Background: The proliferation of publicly accessible large-scale biological data together with increasing availability of bioinformatics tools have the potential to transform biomedical research. Here we report a crowdsourcing Jamboree that explored whether a team of volunteer biologists without for...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
F1000Research
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5399965/ https://www.ncbi.nlm.nih.gov/pubmed/28491277 http://dx.doi.org/10.12688/f1000research.10465.1 |
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author | Lau, William W. Sparks, Rachel Tsang, John S. |
author_facet | Lau, William W. Sparks, Rachel Tsang, John S. |
author_sort | Lau, William W. |
collection | PubMed |
description | Background: The proliferation of publicly accessible large-scale biological data together with increasing availability of bioinformatics tools have the potential to transform biomedical research. Here we report a crowdsourcing Jamboree that explored whether a team of volunteer biologists without formal bioinformatics training could use OMiCC, a crowdsourcing web platform that facilitates the reuse and (meta-) analysis of public gene expression data, to compile and annotate gene expression data, and design comparisons between disease and control sample groups. Methods: The Jamboree focused on several common human autoimmune diseases, including systemic lupus erythematosus (SLE), multiple sclerosis (MS), type I diabetes (DM1), and rheumatoid arthritis (RA), and the corresponding mouse models. Meta-analyses were performed in OMiCC using comparisons constructed by the participants to identify 1) gene expression signatures for each disease (disease versus healthy controls at the gene expression and biological pathway levels), 2) conserved signatures across all diseases within each species (pan-disease signatures), and 3) conserved signatures between species for each disease and across all diseases (cross-species signatures). Results: A large number of differentially expressed genes were identified for each disease based on meta-analysis, with observed overlap among diseases both within and across species. Gene set/pathway enrichment of upregulated genes suggested conserved signatures (e.g., interferon) across all human and mouse conditions. Conclusions: Our Jamboree exercise provides evidence that when enabled by appropriate tools, a "crowd" of biologists can work together to accelerate the pace by which the increasingly large amounts of public data can be reused and meta-analyzed for generating and testing hypotheses. Our encouraging experience suggests that a similar crowdsourcing approach can be used to explore other biological questions. |
format | Online Article Text |
id | pubmed-5399965 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | F1000Research |
record_format | MEDLINE/PubMed |
spelling | pubmed-53999652017-05-09 Meta-analysis of crowdsourced data compendia suggests pan-disease transcriptional signatures of autoimmunity Lau, William W. Sparks, Rachel Tsang, John S. F1000Res Research Note Background: The proliferation of publicly accessible large-scale biological data together with increasing availability of bioinformatics tools have the potential to transform biomedical research. Here we report a crowdsourcing Jamboree that explored whether a team of volunteer biologists without formal bioinformatics training could use OMiCC, a crowdsourcing web platform that facilitates the reuse and (meta-) analysis of public gene expression data, to compile and annotate gene expression data, and design comparisons between disease and control sample groups. Methods: The Jamboree focused on several common human autoimmune diseases, including systemic lupus erythematosus (SLE), multiple sclerosis (MS), type I diabetes (DM1), and rheumatoid arthritis (RA), and the corresponding mouse models. Meta-analyses were performed in OMiCC using comparisons constructed by the participants to identify 1) gene expression signatures for each disease (disease versus healthy controls at the gene expression and biological pathway levels), 2) conserved signatures across all diseases within each species (pan-disease signatures), and 3) conserved signatures between species for each disease and across all diseases (cross-species signatures). Results: A large number of differentially expressed genes were identified for each disease based on meta-analysis, with observed overlap among diseases both within and across species. Gene set/pathway enrichment of upregulated genes suggested conserved signatures (e.g., interferon) across all human and mouse conditions. Conclusions: Our Jamboree exercise provides evidence that when enabled by appropriate tools, a "crowd" of biologists can work together to accelerate the pace by which the increasingly large amounts of public data can be reused and meta-analyzed for generating and testing hypotheses. Our encouraging experience suggests that a similar crowdsourcing approach can be used to explore other biological questions. F1000Research 2016-12-20 /pmc/articles/PMC5399965/ /pubmed/28491277 http://dx.doi.org/10.12688/f1000research.10465.1 Text en Copyright: © 2016 Lau WW et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The author(s) is/are employees of the US Government and therefore domestic copyright protection in USA does not apply to this work. The work may be protected under the copyright laws of other jurisdictions when used in those jurisdictions. |
spellingShingle | Research Note Lau, William W. Sparks, Rachel Tsang, John S. Meta-analysis of crowdsourced data compendia suggests pan-disease transcriptional signatures of autoimmunity |
title | Meta-analysis of crowdsourced data compendia suggests pan-disease transcriptional signatures of autoimmunity |
title_full | Meta-analysis of crowdsourced data compendia suggests pan-disease transcriptional signatures of autoimmunity |
title_fullStr | Meta-analysis of crowdsourced data compendia suggests pan-disease transcriptional signatures of autoimmunity |
title_full_unstemmed | Meta-analysis of crowdsourced data compendia suggests pan-disease transcriptional signatures of autoimmunity |
title_short | Meta-analysis of crowdsourced data compendia suggests pan-disease transcriptional signatures of autoimmunity |
title_sort | meta-analysis of crowdsourced data compendia suggests pan-disease transcriptional signatures of autoimmunity |
topic | Research Note |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5399965/ https://www.ncbi.nlm.nih.gov/pubmed/28491277 http://dx.doi.org/10.12688/f1000research.10465.1 |
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