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OmicsVis: an interactive tool for visually analyzing metabolomics data
When analyzing metabolomics data, cancer care researchers are searching for differences between known healthy samples and unhealthy samples. By analyzing and understanding these differences, researchers hope to identify cancer biomarkers. Due to the size and complexity of the data produced, however,...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3355336/ https://www.ncbi.nlm.nih.gov/pubmed/22607515 http://dx.doi.org/10.1186/1471-2105-13-S8-S6 |
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author | Livengood, Philip Maciejewski, Ross Chen, Wei Ebert, David S |
author_facet | Livengood, Philip Maciejewski, Ross Chen, Wei Ebert, David S |
author_sort | Livengood, Philip |
collection | PubMed |
description | When analyzing metabolomics data, cancer care researchers are searching for differences between known healthy samples and unhealthy samples. By analyzing and understanding these differences, researchers hope to identify cancer biomarkers. Due to the size and complexity of the data produced, however, analysis can still be very slow and time consuming. This is further complicated by the fact that datasets obtained will exhibit incidental differences in intensity and retention time, not related to actual chemical differences in the samples being evaluated. Additionally, automated tools to correct these errors do not always produce reliable results. This work presents a new analytics system that enables interactive comparative visualization and analytics of metabolomics data obtained by two-dimensional gas chromatography-mass spectrometry (GC × GC-MS). The key features of this system are the ability to produce visualizations of multiple GC × GC-MS data sets, and to explore those data sets interactively, allowing a user to discover differences and features in real time. The system provides statistical support in the form of difference, standard deviation, and kernel density estimation calculations to aid users in identifying meaningful differences between samples. These are combined with novel transfer functions and multiform, linked visualizations in order to provide researchers with a powerful new tool for GC × GC-MS exploration and bio-marker discovery. |
format | Online Article Text |
id | pubmed-3355336 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-33553362012-05-18 OmicsVis: an interactive tool for visually analyzing metabolomics data Livengood, Philip Maciejewski, Ross Chen, Wei Ebert, David S BMC Bioinformatics Research When analyzing metabolomics data, cancer care researchers are searching for differences between known healthy samples and unhealthy samples. By analyzing and understanding these differences, researchers hope to identify cancer biomarkers. Due to the size and complexity of the data produced, however, analysis can still be very slow and time consuming. This is further complicated by the fact that datasets obtained will exhibit incidental differences in intensity and retention time, not related to actual chemical differences in the samples being evaluated. Additionally, automated tools to correct these errors do not always produce reliable results. This work presents a new analytics system that enables interactive comparative visualization and analytics of metabolomics data obtained by two-dimensional gas chromatography-mass spectrometry (GC × GC-MS). The key features of this system are the ability to produce visualizations of multiple GC × GC-MS data sets, and to explore those data sets interactively, allowing a user to discover differences and features in real time. The system provides statistical support in the form of difference, standard deviation, and kernel density estimation calculations to aid users in identifying meaningful differences between samples. These are combined with novel transfer functions and multiform, linked visualizations in order to provide researchers with a powerful new tool for GC × GC-MS exploration and bio-marker discovery. BioMed Central 2012-05-18 /pmc/articles/PMC3355336/ /pubmed/22607515 http://dx.doi.org/10.1186/1471-2105-13-S8-S6 Text en Copyright ©2012 Livengood et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Livengood, Philip Maciejewski, Ross Chen, Wei Ebert, David S OmicsVis: an interactive tool for visually analyzing metabolomics data |
title | OmicsVis: an interactive tool for visually analyzing metabolomics data |
title_full | OmicsVis: an interactive tool for visually analyzing metabolomics data |
title_fullStr | OmicsVis: an interactive tool for visually analyzing metabolomics data |
title_full_unstemmed | OmicsVis: an interactive tool for visually analyzing metabolomics data |
title_short | OmicsVis: an interactive tool for visually analyzing metabolomics data |
title_sort | omicsvis: an interactive tool for visually analyzing metabolomics data |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3355336/ https://www.ncbi.nlm.nih.gov/pubmed/22607515 http://dx.doi.org/10.1186/1471-2105-13-S8-S6 |
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