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GeneAnalytics: An Integrative Gene Set Analysis Tool for Next Generation Sequencing, RNAseq and Microarray Data

Postgenomics data are produced in large volumes by life sciences and clinical applications of novel omics diagnostics and therapeutics for precision medicine. To move from “data-to-knowledge-to-innovation,” a crucial missing step in the current era is, however, our limited understanding of biologica...

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Autores principales: Ben-Ari Fuchs, Shani, Lieder, Iris, Stelzer, Gil, Mazor, Yaron, Buzhor, Ella, Kaplan, Sergey, Bogoch, Yoel, Plaschkes, Inbar, Shitrit, Alina, Rappaport, Noa, Kohn, Asher, Edgar, Ron, Shenhav, Liraz, Safran, Marilyn, Lancet, Doron, Guan-Golan, Yaron, Warshawsky, David, Shtrichman, Ronit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mary Ann Liebert, Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4799705/
https://www.ncbi.nlm.nih.gov/pubmed/26983021
http://dx.doi.org/10.1089/omi.2015.0168
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author Ben-Ari Fuchs, Shani
Lieder, Iris
Stelzer, Gil
Mazor, Yaron
Buzhor, Ella
Kaplan, Sergey
Bogoch, Yoel
Plaschkes, Inbar
Shitrit, Alina
Rappaport, Noa
Kohn, Asher
Edgar, Ron
Shenhav, Liraz
Safran, Marilyn
Lancet, Doron
Guan-Golan, Yaron
Warshawsky, David
Shtrichman, Ronit
author_facet Ben-Ari Fuchs, Shani
Lieder, Iris
Stelzer, Gil
Mazor, Yaron
Buzhor, Ella
Kaplan, Sergey
Bogoch, Yoel
Plaschkes, Inbar
Shitrit, Alina
Rappaport, Noa
Kohn, Asher
Edgar, Ron
Shenhav, Liraz
Safran, Marilyn
Lancet, Doron
Guan-Golan, Yaron
Warshawsky, David
Shtrichman, Ronit
author_sort Ben-Ari Fuchs, Shani
collection PubMed
description Postgenomics data are produced in large volumes by life sciences and clinical applications of novel omics diagnostics and therapeutics for precision medicine. To move from “data-to-knowledge-to-innovation,” a crucial missing step in the current era is, however, our limited understanding of biological and clinical contexts associated with data. Prominent among the emerging remedies to this challenge are the gene set enrichment tools. This study reports on GeneAnalytics™ (geneanalytics.genecards.org), a comprehensive and easy-to-apply gene set analysis tool for rapid contextualization of expression patterns and functional signatures embedded in the postgenomics Big Data domains, such as Next Generation Sequencing (NGS), RNAseq, and microarray experiments. GeneAnalytics' differentiating features include in-depth evidence-based scoring algorithms, an intuitive user interface and proprietary unified data. GeneAnalytics employs the LifeMap Science's GeneCards suite, including the GeneCards®—the human gene database; the MalaCards—the human diseases database; and the PathCards—the biological pathways database. Expression-based analysis in GeneAnalytics relies on the LifeMap Discovery®—the embryonic development and stem cells database, which includes manually curated expression data for normal and diseased tissues, enabling advanced matching algorithm for gene–tissue association. This assists in evaluating differentiation protocols and discovering biomarkers for tissues and cells. Results are directly linked to gene, disease, or cell “cards” in the GeneCards suite. Future developments aim to enhance the GeneAnalytics algorithm as well as visualizations, employing varied graphical display items. Such attributes make GeneAnalytics a broadly applicable postgenomics data analyses and interpretation tool for translation of data to knowledge-based innovation in various Big Data fields such as precision medicine, ecogenomics, nutrigenomics, pharmacogenomics, vaccinomics, and others yet to emerge on the postgenomics horizon.
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spelling pubmed-47997052016-03-24 GeneAnalytics: An Integrative Gene Set Analysis Tool for Next Generation Sequencing, RNAseq and Microarray Data Ben-Ari Fuchs, Shani Lieder, Iris Stelzer, Gil Mazor, Yaron Buzhor, Ella Kaplan, Sergey Bogoch, Yoel Plaschkes, Inbar Shitrit, Alina Rappaport, Noa Kohn, Asher Edgar, Ron Shenhav, Liraz Safran, Marilyn Lancet, Doron Guan-Golan, Yaron Warshawsky, David Shtrichman, Ronit OMICS Original Articles Postgenomics data are produced in large volumes by life sciences and clinical applications of novel omics diagnostics and therapeutics for precision medicine. To move from “data-to-knowledge-to-innovation,” a crucial missing step in the current era is, however, our limited understanding of biological and clinical contexts associated with data. Prominent among the emerging remedies to this challenge are the gene set enrichment tools. This study reports on GeneAnalytics™ (geneanalytics.genecards.org), a comprehensive and easy-to-apply gene set analysis tool for rapid contextualization of expression patterns and functional signatures embedded in the postgenomics Big Data domains, such as Next Generation Sequencing (NGS), RNAseq, and microarray experiments. GeneAnalytics' differentiating features include in-depth evidence-based scoring algorithms, an intuitive user interface and proprietary unified data. GeneAnalytics employs the LifeMap Science's GeneCards suite, including the GeneCards®—the human gene database; the MalaCards—the human diseases database; and the PathCards—the biological pathways database. Expression-based analysis in GeneAnalytics relies on the LifeMap Discovery®—the embryonic development and stem cells database, which includes manually curated expression data for normal and diseased tissues, enabling advanced matching algorithm for gene–tissue association. This assists in evaluating differentiation protocols and discovering biomarkers for tissues and cells. Results are directly linked to gene, disease, or cell “cards” in the GeneCards suite. Future developments aim to enhance the GeneAnalytics algorithm as well as visualizations, employing varied graphical display items. Such attributes make GeneAnalytics a broadly applicable postgenomics data analyses and interpretation tool for translation of data to knowledge-based innovation in various Big Data fields such as precision medicine, ecogenomics, nutrigenomics, pharmacogenomics, vaccinomics, and others yet to emerge on the postgenomics horizon. Mary Ann Liebert, Inc. 2016-03-01 /pmc/articles/PMC4799705/ /pubmed/26983021 http://dx.doi.org/10.1089/omi.2015.0168 Text en © Shani Ben-Ari Fuchs, et al., 2016. Published by Mary Ann Liebert, Inc. This Open Access article is distributed under the terms of the Creative Commons Attribution Noncommercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Original Articles
Ben-Ari Fuchs, Shani
Lieder, Iris
Stelzer, Gil
Mazor, Yaron
Buzhor, Ella
Kaplan, Sergey
Bogoch, Yoel
Plaschkes, Inbar
Shitrit, Alina
Rappaport, Noa
Kohn, Asher
Edgar, Ron
Shenhav, Liraz
Safran, Marilyn
Lancet, Doron
Guan-Golan, Yaron
Warshawsky, David
Shtrichman, Ronit
GeneAnalytics: An Integrative Gene Set Analysis Tool for Next Generation Sequencing, RNAseq and Microarray Data
title GeneAnalytics: An Integrative Gene Set Analysis Tool for Next Generation Sequencing, RNAseq and Microarray Data
title_full GeneAnalytics: An Integrative Gene Set Analysis Tool for Next Generation Sequencing, RNAseq and Microarray Data
title_fullStr GeneAnalytics: An Integrative Gene Set Analysis Tool for Next Generation Sequencing, RNAseq and Microarray Data
title_full_unstemmed GeneAnalytics: An Integrative Gene Set Analysis Tool for Next Generation Sequencing, RNAseq and Microarray Data
title_short GeneAnalytics: An Integrative Gene Set Analysis Tool for Next Generation Sequencing, RNAseq and Microarray Data
title_sort geneanalytics: an integrative gene set analysis tool for next generation sequencing, rnaseq and microarray data
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4799705/
https://www.ncbi.nlm.nih.gov/pubmed/26983021
http://dx.doi.org/10.1089/omi.2015.0168
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