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MiSTIC, an integrated platform for the analysis of heterogeneity in large tumour transcriptome datasets
Genome-wide transcriptome profiling has enabled non-supervised classification of tumours, revealing different sub-groups characterized by specific gene expression features. However, the biological significance of these subtypes remains for the most part unclear. We describe herein an interactive pla...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5570030/ https://www.ncbi.nlm.nih.gov/pubmed/28472340 http://dx.doi.org/10.1093/nar/gkx338 |
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author | Lemieux, Sebastien Sargeant, Tobias Laperrière, David Ismail, Houssam Boucher, Geneviève Rozendaal, Marieke Lavallée, Vincent-Philippe Ashton-Beaucage, Dariel Wilhelm, Brian Hébert, Josée Hilton, Douglas J. Mader, Sylvie Sauvageau, Guy |
author_facet | Lemieux, Sebastien Sargeant, Tobias Laperrière, David Ismail, Houssam Boucher, Geneviève Rozendaal, Marieke Lavallée, Vincent-Philippe Ashton-Beaucage, Dariel Wilhelm, Brian Hébert, Josée Hilton, Douglas J. Mader, Sylvie Sauvageau, Guy |
author_sort | Lemieux, Sebastien |
collection | PubMed |
description | Genome-wide transcriptome profiling has enabled non-supervised classification of tumours, revealing different sub-groups characterized by specific gene expression features. However, the biological significance of these subtypes remains for the most part unclear. We describe herein an interactive platform, Minimum Spanning Trees Inferred Clustering (MiSTIC), that integrates the direct visualization and comparison of the gene correlation structure between datasets, the analysis of the molecular causes underlying co-variations in gene expression in cancer samples, and the clinical annotation of tumour sets defined by the combined expression of selected biomarkers. We have used MiSTIC to highlight the roles of specific transcription factors in breast cancer subtype specification, to compare the aspects of tumour heterogeneity targeted by different prognostic signatures, and to highlight biomarker interactions in AML. A version of MiSTIC preloaded with datasets described herein can be accessed through a public web server (http://mistic.iric.ca); in addition, the MiSTIC software package can be obtained (github.com/iric-soft/MiSTIC) for local use with personalized datasets. |
format | Online Article Text |
id | pubmed-5570030 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-55700302017-08-29 MiSTIC, an integrated platform for the analysis of heterogeneity in large tumour transcriptome datasets Lemieux, Sebastien Sargeant, Tobias Laperrière, David Ismail, Houssam Boucher, Geneviève Rozendaal, Marieke Lavallée, Vincent-Philippe Ashton-Beaucage, Dariel Wilhelm, Brian Hébert, Josée Hilton, Douglas J. Mader, Sylvie Sauvageau, Guy Nucleic Acids Res Methods Online Genome-wide transcriptome profiling has enabled non-supervised classification of tumours, revealing different sub-groups characterized by specific gene expression features. However, the biological significance of these subtypes remains for the most part unclear. We describe herein an interactive platform, Minimum Spanning Trees Inferred Clustering (MiSTIC), that integrates the direct visualization and comparison of the gene correlation structure between datasets, the analysis of the molecular causes underlying co-variations in gene expression in cancer samples, and the clinical annotation of tumour sets defined by the combined expression of selected biomarkers. We have used MiSTIC to highlight the roles of specific transcription factors in breast cancer subtype specification, to compare the aspects of tumour heterogeneity targeted by different prognostic signatures, and to highlight biomarker interactions in AML. A version of MiSTIC preloaded with datasets described herein can be accessed through a public web server (http://mistic.iric.ca); in addition, the MiSTIC software package can be obtained (github.com/iric-soft/MiSTIC) for local use with personalized datasets. Oxford University Press 2017-07-27 2017-05-04 /pmc/articles/PMC5570030/ /pubmed/28472340 http://dx.doi.org/10.1093/nar/gkx338 Text en © The Author(s) 2017. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution 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 | Methods Online Lemieux, Sebastien Sargeant, Tobias Laperrière, David Ismail, Houssam Boucher, Geneviève Rozendaal, Marieke Lavallée, Vincent-Philippe Ashton-Beaucage, Dariel Wilhelm, Brian Hébert, Josée Hilton, Douglas J. Mader, Sylvie Sauvageau, Guy MiSTIC, an integrated platform for the analysis of heterogeneity in large tumour transcriptome datasets |
title | MiSTIC, an integrated platform for the analysis of heterogeneity in large tumour transcriptome datasets |
title_full | MiSTIC, an integrated platform for the analysis of heterogeneity in large tumour transcriptome datasets |
title_fullStr | MiSTIC, an integrated platform for the analysis of heterogeneity in large tumour transcriptome datasets |
title_full_unstemmed | MiSTIC, an integrated platform for the analysis of heterogeneity in large tumour transcriptome datasets |
title_short | MiSTIC, an integrated platform for the analysis of heterogeneity in large tumour transcriptome datasets |
title_sort | mistic, an integrated platform for the analysis of heterogeneity in large tumour transcriptome datasets |
topic | Methods Online |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5570030/ https://www.ncbi.nlm.nih.gov/pubmed/28472340 http://dx.doi.org/10.1093/nar/gkx338 |
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