PROMO: an interactive tool for analyzing clinically-labeled multi-omic cancer datasets

Abstract Background Analysis of large genomic datasets along with their accompanying clinical information has shown great promise in cancer research over the last decade. Such datasets typically include thousands of samples, each measured by one or several high-throughput technologies (‘omics’) and...

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Main Authors: Dvir Netanely, Neta Stern, Itay Laufer, Ron Shamir
Format: Article
Language:English
Published: BMC 2019-12-01
Series:BMC Bioinformatics
Subjects:
Online Access:https://doi.org/10.1186/s12859-019-3142-5
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spelling doaj-9fcc66a33aa14874ad3add54abd3f8752020-12-27T12:21:49ZengBMCBMC Bioinformatics1471-21052019-12-0120111010.1186/s12859-019-3142-5PROMO: an interactive tool for analyzing clinically-labeled multi-omic cancer datasetsDvir Netanely0Neta Stern1Itay Laufer2Ron Shamir3Blavatnik School of Computer Science, Tel Aviv UniversityBlavatnik School of Computer Science, Tel Aviv UniversityBlavatnik School of Computer Science, Tel Aviv UniversityBlavatnik School of Computer Science, Tel Aviv UniversityAbstract Background Analysis of large genomic datasets along with their accompanying clinical information has shown great promise in cancer research over the last decade. Such datasets typically include thousands of samples, each measured by one or several high-throughput technologies (‘omics’) and annotated with extensive clinical information. While instrumental for fulfilling the promise of personalized medicine, the analysis and visualization of such large datasets is challenging and necessitates programming skills and familiarity with a large array of software tools to be used for the various steps of the analysis. Results We developed PROMO (Profiler of Multi-Omic data), a friendly, fully interactive stand-alone software for analyzing large genomic cancer datasets together with their associated clinical information. The tool provides an array of built-in methods and algorithms for importing, preprocessing, visualizing, clustering, clinical label enrichment testing, and survival analysis that can be performed on a single or multi-omic dataset. The tool can be used for quick exploration and stratification of tumor samples taken from patients into clinically significant molecular subtypes. Identification of prognostic biomarkers and generation of simple subtype classifiers are additional important features. We review PROMO’s main features and demonstrate its analysis capabilities on a breast cancer cohort from TCGA. Conclusions PROMO provides a single integrated solution for swiftly performing a complete analysis of cancer genomic data for subtype discovery and biomarker identification without writing a single line of code, and can, therefore, make the analysis of these data much easier for cancer biologists and biomedical researchers. PROMO is freely available for download at http://acgt.cs.tau.ac.il/promo/.https://doi.org/10.1186/s12859-019-3142-5Cancer genomicsPersonalized medicineCancer subtypesMulti-omicsCancer biomarkersMulti-omic clustering
collection DOAJ
language English
format Article
sources DOAJ
author Dvir Netanely
Neta Stern
Itay Laufer
Ron Shamir
spellingShingle Dvir Netanely
Neta Stern
Itay Laufer
Ron Shamir
PROMO: an interactive tool for analyzing clinically-labeled multi-omic cancer datasets
BMC Bioinformatics
Cancer genomics
Personalized medicine
Cancer subtypes
Multi-omics
Cancer biomarkers
Multi-omic clustering
author_facet Dvir Netanely
Neta Stern
Itay Laufer
Ron Shamir
author_sort Dvir Netanely
title PROMO: an interactive tool for analyzing clinically-labeled multi-omic cancer datasets
title_short PROMO: an interactive tool for analyzing clinically-labeled multi-omic cancer datasets
title_full PROMO: an interactive tool for analyzing clinically-labeled multi-omic cancer datasets
title_fullStr PROMO: an interactive tool for analyzing clinically-labeled multi-omic cancer datasets
title_full_unstemmed PROMO: an interactive tool for analyzing clinically-labeled multi-omic cancer datasets
title_sort promo: an interactive tool for analyzing clinically-labeled multi-omic cancer datasets
publisher BMC
series BMC Bioinformatics
issn 1471-2105
publishDate 2019-12-01
description Abstract Background Analysis of large genomic datasets along with their accompanying clinical information has shown great promise in cancer research over the last decade. Such datasets typically include thousands of samples, each measured by one or several high-throughput technologies (‘omics’) and annotated with extensive clinical information. While instrumental for fulfilling the promise of personalized medicine, the analysis and visualization of such large datasets is challenging and necessitates programming skills and familiarity with a large array of software tools to be used for the various steps of the analysis. Results We developed PROMO (Profiler of Multi-Omic data), a friendly, fully interactive stand-alone software for analyzing large genomic cancer datasets together with their associated clinical information. The tool provides an array of built-in methods and algorithms for importing, preprocessing, visualizing, clustering, clinical label enrichment testing, and survival analysis that can be performed on a single or multi-omic dataset. The tool can be used for quick exploration and stratification of tumor samples taken from patients into clinically significant molecular subtypes. Identification of prognostic biomarkers and generation of simple subtype classifiers are additional important features. We review PROMO’s main features and demonstrate its analysis capabilities on a breast cancer cohort from TCGA. Conclusions PROMO provides a single integrated solution for swiftly performing a complete analysis of cancer genomic data for subtype discovery and biomarker identification without writing a single line of code, and can, therefore, make the analysis of these data much easier for cancer biologists and biomedical researchers. PROMO is freely available for download at http://acgt.cs.tau.ac.il/promo/.
topic Cancer genomics
Personalized medicine
Cancer subtypes
Multi-omics
Cancer biomarkers
Multi-omic clustering
url https://doi.org/10.1186/s12859-019-3142-5
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