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GenomeCAT: a versatile tool for the analysis and integrative visualization of DNA copy number variants

BACKGROUND: The analysis of DNA copy number variants (CNV) has increasing impact in the field of genetic diagnostics and research. However, the interpretation of CNV data derived from high resolution array CGH or NGS platforms is complicated by the considerable variability of the human genome. There...

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Autores principales: Tebel, Katrin, Boldt, Vivien, Steininger, Anne, Port, Matthias, Ebert, Grit, Ullmann, Reinhard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5217618/
https://www.ncbi.nlm.nih.gov/pubmed/28061750
http://dx.doi.org/10.1186/s12859-016-1430-x
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author Tebel, Katrin
Boldt, Vivien
Steininger, Anne
Port, Matthias
Ebert, Grit
Ullmann, Reinhard
author_facet Tebel, Katrin
Boldt, Vivien
Steininger, Anne
Port, Matthias
Ebert, Grit
Ullmann, Reinhard
author_sort Tebel, Katrin
collection PubMed
description BACKGROUND: The analysis of DNA copy number variants (CNV) has increasing impact in the field of genetic diagnostics and research. However, the interpretation of CNV data derived from high resolution array CGH or NGS platforms is complicated by the considerable variability of the human genome. Therefore, tools for multidimensional data analysis and comparison of patient cohorts are needed to assist in the discrimination of clinically relevant CNVs from others. RESULTS: We developed GenomeCAT, a standalone Java application for the analysis and integrative visualization of CNVs. GenomeCAT is composed of three modules dedicated to the inspection of single cases, comparative analysis of multidimensional data and group comparisons aiming at the identification of recurrent aberrations in patients sharing the same phenotype, respectively. Its flexible import options ease the comparative analysis of own results derived from microarray or NGS platforms with data from literature or public depositories. Multidimensional data obtained from different experiment types can be merged into a common data matrix to enable common visualization and analysis. All results are stored in the integrated MySQL database, but can also be exported as tab delimited files for further statistical calculations in external programs. CONCLUSIONS: GenomeCAT offers a broad spectrum of visualization and analysis tools that assist in the evaluation of CNVs in the context of other experiment data and annotations. The use of GenomeCAT does not require any specialized computer skills. The various R packages implemented for data analysis are fully integrated into GenomeCATs graphical user interface and the installation process is supported by a wizard. The flexibility in terms of data import and export in combination with the ability to create a common data matrix makes the program also well suited as an interface between genomic data from heterogeneous sources and external software tools. Due to the modular architecture the functionality of GenomeCAT can be easily extended by further R packages or customized plug-ins to meet future requirements. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12859-016-1430-x) contains supplementary material, which is available to authorized users.
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spelling pubmed-52176182017-01-09 GenomeCAT: a versatile tool for the analysis and integrative visualization of DNA copy number variants Tebel, Katrin Boldt, Vivien Steininger, Anne Port, Matthias Ebert, Grit Ullmann, Reinhard BMC Bioinformatics Software BACKGROUND: The analysis of DNA copy number variants (CNV) has increasing impact in the field of genetic diagnostics and research. However, the interpretation of CNV data derived from high resolution array CGH or NGS platforms is complicated by the considerable variability of the human genome. Therefore, tools for multidimensional data analysis and comparison of patient cohorts are needed to assist in the discrimination of clinically relevant CNVs from others. RESULTS: We developed GenomeCAT, a standalone Java application for the analysis and integrative visualization of CNVs. GenomeCAT is composed of three modules dedicated to the inspection of single cases, comparative analysis of multidimensional data and group comparisons aiming at the identification of recurrent aberrations in patients sharing the same phenotype, respectively. Its flexible import options ease the comparative analysis of own results derived from microarray or NGS platforms with data from literature or public depositories. Multidimensional data obtained from different experiment types can be merged into a common data matrix to enable common visualization and analysis. All results are stored in the integrated MySQL database, but can also be exported as tab delimited files for further statistical calculations in external programs. CONCLUSIONS: GenomeCAT offers a broad spectrum of visualization and analysis tools that assist in the evaluation of CNVs in the context of other experiment data and annotations. The use of GenomeCAT does not require any specialized computer skills. The various R packages implemented for data analysis are fully integrated into GenomeCATs graphical user interface and the installation process is supported by a wizard. The flexibility in terms of data import and export in combination with the ability to create a common data matrix makes the program also well suited as an interface between genomic data from heterogeneous sources and external software tools. Due to the modular architecture the functionality of GenomeCAT can be easily extended by further R packages or customized plug-ins to meet future requirements. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12859-016-1430-x) contains supplementary material, which is available to authorized users. BioMed Central 2017-01-06 /pmc/articles/PMC5217618/ /pubmed/28061750 http://dx.doi.org/10.1186/s12859-016-1430-x Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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 Software
Tebel, Katrin
Boldt, Vivien
Steininger, Anne
Port, Matthias
Ebert, Grit
Ullmann, Reinhard
GenomeCAT: a versatile tool for the analysis and integrative visualization of DNA copy number variants
title GenomeCAT: a versatile tool for the analysis and integrative visualization of DNA copy number variants
title_full GenomeCAT: a versatile tool for the analysis and integrative visualization of DNA copy number variants
title_fullStr GenomeCAT: a versatile tool for the analysis and integrative visualization of DNA copy number variants
title_full_unstemmed GenomeCAT: a versatile tool for the analysis and integrative visualization of DNA copy number variants
title_short GenomeCAT: a versatile tool for the analysis and integrative visualization of DNA copy number variants
title_sort genomecat: a versatile tool for the analysis and integrative visualization of dna copy number variants
topic Software
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5217618/
https://www.ncbi.nlm.nih.gov/pubmed/28061750
http://dx.doi.org/10.1186/s12859-016-1430-x
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