G-DOC Plus – an integrative bioinformatics platform for precision medicine. Issue 1 (December 2016)
- Record Type:
- Journal Article
- Title:
- G-DOC Plus – an integrative bioinformatics platform for precision medicine. Issue 1 (December 2016)
- Main Title:
- G-DOC Plus – an integrative bioinformatics platform for precision medicine
- Authors:
- Bhuvaneshwar, Krithika
Belouali, Anas
Singh, Varun
Johnson, Robert
Song, Lei
Alaoui, Adil
Harris, Michael
Clarke, Robert
Weiner, Louis
Gusev, Yuriy
Madhavan, Subha - Abstract:
- Abstract Background G-DOCPlus is a data integration and bioinformatics platform that uses cloud computing and other advanced computational tools to handle a variety of biomedical BIG DATA including gene expression arrays, NGS and medical images so that they can be analyzed in the full context of other omics and clinical information. Results G-DOCPlus currently holds data from over 10, 000 patients selected from private and public resources including Gene Expression Omnibus (GEO), The Cancer Genome Atlas (TCGA) and the recently added datasets from REpository for Molecular BRAin Neoplasia DaTa (REMBRANDT), caArray studies of lung and colon cancer, ImmPort and the 1000 genomes data sets. The system allows researchers to explore clinical-omic data one sample at a time, as a cohort of samples; or at the level of population, providing the user with a comprehensive view of the data. G-DOCPlus tools have been leveraged in cancer and non-cancer studies for hypothesis generation and validation; biomarker discovery and multi-omics analysis, to explore somatic mutations and cancer MRI images; as well as for training and graduate education in bioinformatics, data and computational sciences. Several of these use cases are described in this paper to demonstrate its multifaceted usability. Conclusion G-DOCPlus can be used to support a variety of user groups in multiple domains to enable hypothesis generation for precision medicine research. The long-term vision of G-DOCPlus is to extendAbstract Background G-DOCPlus is a data integration and bioinformatics platform that uses cloud computing and other advanced computational tools to handle a variety of biomedical BIG DATA including gene expression arrays, NGS and medical images so that they can be analyzed in the full context of other omics and clinical information. Results G-DOCPlus currently holds data from over 10, 000 patients selected from private and public resources including Gene Expression Omnibus (GEO), The Cancer Genome Atlas (TCGA) and the recently added datasets from REpository for Molecular BRAin Neoplasia DaTa (REMBRANDT), caArray studies of lung and colon cancer, ImmPort and the 1000 genomes data sets. The system allows researchers to explore clinical-omic data one sample at a time, as a cohort of samples; or at the level of population, providing the user with a comprehensive view of the data. G-DOCPlus tools have been leveraged in cancer and non-cancer studies for hypothesis generation and validation; biomarker discovery and multi-omics analysis, to explore somatic mutations and cancer MRI images; as well as for training and graduate education in bioinformatics, data and computational sciences. Several of these use cases are described in this paper to demonstrate its multifaceted usability. Conclusion G-DOCPlus can be used to support a variety of user groups in multiple domains to enable hypothesis generation for precision medicine research. The long-term vision of G-DOCPlus is to extend this translational bioinformatics platform to stay current with emerging omics technologies and analysis methods to continue supporting novel hypothesis generation, analysis and validation for integrative biomedical research. By integrating several aspects of the disease and exposing various data elements, such as outpatient lab workup, pathology, radiology, current treatments, molecular signatures and expected outcomes over a web interface, G-DOCPlus will continue to strengthen precision medicine research. G-DOCPlus is available at:https://gdoc.georgetown.edu . … (more)
- Is Part Of:
- BMC bioinformatics. Volume 17:Issue 1(2016)
- Journal:
- BMC bioinformatics
- Issue:
- Volume 17:Issue 1(2016)
- Issue Display:
- Volume 17, Issue 1 (2016)
- Year:
- 2016
- Volume:
- 17
- Issue:
- 1
- Issue Sort Value:
- 2016-0017-0001-0000
- Page Start:
- 1
- Page End:
- 13
- Publication Date:
- 2016-12
- Subjects:
- Bioinformatics -- Translational research -- Precision medicine -- Cloud computing -- Variant analysis -- Next generation sequencing -- Outcomes research -- Genotype-phenotype integration
Bioinformatics -- Periodicals
Computational biology -- Periodicals
570.285 - Journal URLs:
- http://www.biomedcentral.com/bmcbioinformatics/ ↗
http://www.pubmedcentral.nih.gov/tocrender.fcgi?journal=13 ↗
http://link.springer.com/ ↗ - DOI:
- 10.1186/s12859-016-1010-0 ↗
- Languages:
- English
- ISSNs:
- 1471-2105
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
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- 9952.xml