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A new tool CovReport generates easy-to-understand sequencing coverage summary for diagnostic reports

In order to properly interpret the results of a diagnostic gene panel sequencing test, gene coverage needs to be taken into consideration. If coverage is too low, an additional re-sequencing test is needed to make sure that a pathogenic variant is not missed. To facilitate the interpretation of cove...

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Autores principales: Gorokhov, Mark, Cerino, Mathieu, Mortreux, Jérémie, Riccardi, Florence, Lévy, Nicolas, Bartoli, Marc, Krahn, Martin, Gorokhova, Svetlana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7148332/
https://www.ncbi.nlm.nih.gov/pubmed/32277129
http://dx.doi.org/10.1038/s41598-020-63079-4
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author Gorokhov, Mark
Cerino, Mathieu
Mortreux, Jérémie
Riccardi, Florence
Lévy, Nicolas
Bartoli, Marc
Krahn, Martin
Gorokhova, Svetlana
author_facet Gorokhov, Mark
Cerino, Mathieu
Mortreux, Jérémie
Riccardi, Florence
Lévy, Nicolas
Bartoli, Marc
Krahn, Martin
Gorokhova, Svetlana
author_sort Gorokhov, Mark
collection PubMed
description In order to properly interpret the results of a diagnostic gene panel sequencing test, gene coverage needs to be taken into consideration. If coverage is too low, an additional re-sequencing test is needed to make sure that a pathogenic variant is not missed. To facilitate the interpretation of coverage data, we designed CovReport, a novel easy-to-use visualization tool. CovReport generates a concise coverage summary that allows one-glance assessment of the sequencing test performance. Both gene-level and exon-level coverage can be immediately appreciated and taken into consideration for further medical decisions. CovReport does not require complex installation and can thus be easily implemented in any diagnostic laboratory setting. A user-friendly interface generates a graphic summary of coverage that can be directly included in the diagnostic report. In addition to a stand-alone version, we also provide a command line version of CovReport that can be integrated into any bioinformatics pipeline. This flexible tool is now part of routine sequencing analysis at the Department of Medical Genetics at La Timone Hospital (Marseille, France). CovReport is available at http://jdotsoft.com/CovReport.php. It is implemented in Java and supported on Windows, Mac OS X and Linux.
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spelling pubmed-71483322020-04-15 A new tool CovReport generates easy-to-understand sequencing coverage summary for diagnostic reports Gorokhov, Mark Cerino, Mathieu Mortreux, Jérémie Riccardi, Florence Lévy, Nicolas Bartoli, Marc Krahn, Martin Gorokhova, Svetlana Sci Rep Article In order to properly interpret the results of a diagnostic gene panel sequencing test, gene coverage needs to be taken into consideration. If coverage is too low, an additional re-sequencing test is needed to make sure that a pathogenic variant is not missed. To facilitate the interpretation of coverage data, we designed CovReport, a novel easy-to-use visualization tool. CovReport generates a concise coverage summary that allows one-glance assessment of the sequencing test performance. Both gene-level and exon-level coverage can be immediately appreciated and taken into consideration for further medical decisions. CovReport does not require complex installation and can thus be easily implemented in any diagnostic laboratory setting. A user-friendly interface generates a graphic summary of coverage that can be directly included in the diagnostic report. In addition to a stand-alone version, we also provide a command line version of CovReport that can be integrated into any bioinformatics pipeline. This flexible tool is now part of routine sequencing analysis at the Department of Medical Genetics at La Timone Hospital (Marseille, France). CovReport is available at http://jdotsoft.com/CovReport.php. It is implemented in Java and supported on Windows, Mac OS X and Linux. Nature Publishing Group UK 2020-04-10 /pmc/articles/PMC7148332/ /pubmed/32277129 http://dx.doi.org/10.1038/s41598-020-63079-4 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Gorokhov, Mark
Cerino, Mathieu
Mortreux, Jérémie
Riccardi, Florence
Lévy, Nicolas
Bartoli, Marc
Krahn, Martin
Gorokhova, Svetlana
A new tool CovReport generates easy-to-understand sequencing coverage summary for diagnostic reports
title A new tool CovReport generates easy-to-understand sequencing coverage summary for diagnostic reports
title_full A new tool CovReport generates easy-to-understand sequencing coverage summary for diagnostic reports
title_fullStr A new tool CovReport generates easy-to-understand sequencing coverage summary for diagnostic reports
title_full_unstemmed A new tool CovReport generates easy-to-understand sequencing coverage summary for diagnostic reports
title_short A new tool CovReport generates easy-to-understand sequencing coverage summary for diagnostic reports
title_sort new tool covreport generates easy-to-understand sequencing coverage summary for diagnostic reports
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7148332/
https://www.ncbi.nlm.nih.gov/pubmed/32277129
http://dx.doi.org/10.1038/s41598-020-63079-4
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