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iGPSe: A visual analytic system for integrative genomic based cancer patient stratification
BACKGROUND: Cancers are highly heterogeneous with different subtypes. These subtypes often possess different genetic variants, present different pathological phenotypes, and most importantly, show various clinical outcomes such as varied prognosis and response to treatment and likelihood for recurre...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4227100/ https://www.ncbi.nlm.nih.gov/pubmed/25000928 http://dx.doi.org/10.1186/1471-2105-15-203 |
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author | Ding, Hao Wang, Chao Huang, Kun Machiraju, Raghu |
author_facet | Ding, Hao Wang, Chao Huang, Kun Machiraju, Raghu |
author_sort | Ding, Hao |
collection | PubMed |
description | BACKGROUND: Cancers are highly heterogeneous with different subtypes. These subtypes often possess different genetic variants, present different pathological phenotypes, and most importantly, show various clinical outcomes such as varied prognosis and response to treatment and likelihood for recurrence and metastasis. Recently, integrative genomics (or panomics) approaches are often adopted with the goal of combining multiple types of omics data to identify integrative biomarkers for stratification of patients into groups with different clinical outcomes. RESULTS: In this paper we present a visual analytic system called Interactive Genomics Patient Stratification explorer (iGPSe) which significantly reduces the computing burden for biomedical researchers in the process of exploring complicated integrative genomics data. Our system integrates unsupervised clustering with graph and parallel sets visualization and allows direct comparison of clinical outcomes via survival analysis. Using a breast cancer dataset obtained from the The Cancer Genome Atlas (TCGA) project, we are able to quickly explore different combinations of gene expression (mRNA) and microRNA features and identify potential combined markers for survival prediction. CONCLUSIONS: Visualization plays an important role in the process of stratifying given population patients. Visual tools allowed for the selection of possibly features across various datasets for the given patient population. We essentially made a case for visualization for a very important problem in translational informatics. |
format | Online Article Text |
id | pubmed-4227100 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42271002014-11-12 iGPSe: A visual analytic system for integrative genomic based cancer patient stratification Ding, Hao Wang, Chao Huang, Kun Machiraju, Raghu BMC Bioinformatics Research Article BACKGROUND: Cancers are highly heterogeneous with different subtypes. These subtypes often possess different genetic variants, present different pathological phenotypes, and most importantly, show various clinical outcomes such as varied prognosis and response to treatment and likelihood for recurrence and metastasis. Recently, integrative genomics (or panomics) approaches are often adopted with the goal of combining multiple types of omics data to identify integrative biomarkers for stratification of patients into groups with different clinical outcomes. RESULTS: In this paper we present a visual analytic system called Interactive Genomics Patient Stratification explorer (iGPSe) which significantly reduces the computing burden for biomedical researchers in the process of exploring complicated integrative genomics data. Our system integrates unsupervised clustering with graph and parallel sets visualization and allows direct comparison of clinical outcomes via survival analysis. Using a breast cancer dataset obtained from the The Cancer Genome Atlas (TCGA) project, we are able to quickly explore different combinations of gene expression (mRNA) and microRNA features and identify potential combined markers for survival prediction. CONCLUSIONS: Visualization plays an important role in the process of stratifying given population patients. Visual tools allowed for the selection of possibly features across various datasets for the given patient population. We essentially made a case for visualization for a very important problem in translational informatics. BioMed Central 2014-07-07 /pmc/articles/PMC4227100/ /pubmed/25000928 http://dx.doi.org/10.1186/1471-2105-15-203 Text en Copyright © 2014 Ding et al.; licensee BioMed Central Ltd. 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 use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Ding, Hao Wang, Chao Huang, Kun Machiraju, Raghu iGPSe: A visual analytic system for integrative genomic based cancer patient stratification |
title | iGPSe: A visual analytic system for integrative genomic based cancer patient stratification |
title_full | iGPSe: A visual analytic system for integrative genomic based cancer patient stratification |
title_fullStr | iGPSe: A visual analytic system for integrative genomic based cancer patient stratification |
title_full_unstemmed | iGPSe: A visual analytic system for integrative genomic based cancer patient stratification |
title_short | iGPSe: A visual analytic system for integrative genomic based cancer patient stratification |
title_sort | igpse: a visual analytic system for integrative genomic based cancer patient stratification |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4227100/ https://www.ncbi.nlm.nih.gov/pubmed/25000928 http://dx.doi.org/10.1186/1471-2105-15-203 |
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