Easymap: A User-Friendly Software Package for Rapid Mapping-by-Sequencing of Point Mutations and Large Insertions

Mapping-by-sequencing strategies combine next-generation sequencing (NGS) with classical linkage analysis, allowing rapid identification of the causal mutations of the phenotypes exhibited by mutants isolated in a genetic screen. Computer programs that analyze NGS data obtained from a mapping popula...

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Main Authors: Samuel Daniel Lup, David Wilson-Sánchez, Sergio Andreu-Sánchez, José Luis Micol
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-05-01
Series:Frontiers in Plant Science
Subjects:
NGS
Online Access:https://www.frontiersin.org/articles/10.3389/fpls.2021.655286/full
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spelling doaj-85e83683aa854afea336b2f518d06bca2021-05-10T16:01:42ZengFrontiers Media S.A.Frontiers in Plant Science1664-462X2021-05-011210.3389/fpls.2021.655286655286Easymap: A User-Friendly Software Package for Rapid Mapping-by-Sequencing of Point Mutations and Large InsertionsSamuel Daniel LupDavid Wilson-SánchezSergio Andreu-SánchezJosé Luis MicolMapping-by-sequencing strategies combine next-generation sequencing (NGS) with classical linkage analysis, allowing rapid identification of the causal mutations of the phenotypes exhibited by mutants isolated in a genetic screen. Computer programs that analyze NGS data obtained from a mapping population of individuals derived from a mutant of interest to identify a causal mutation are available; however, the installation and usage of such programs requires bioinformatic skills, modifying or combining pieces of existing software, or purchasing licenses. To ease this process, we developed Easymap, an open-source program that simplifies the data analysis workflows from raw NGS reads to candidate mutations. Easymap can perform bulked segregant mapping of point mutations induced by ethyl methanesulfonate (EMS) with DNA-seq or RNA-seq datasets, as well as tagged-sequence mapping for large insertions, such as transposons or T-DNAs. The mapping analyses implemented in Easymap have been validated with experimental and simulated datasets from different plant and animal model species. Easymap was designed to be accessible to all users regardless of their bioinformatics skills by implementing a user-friendly graphical interface, a simple universal installation script, and detailed mapping reports, including informative images and complementary data for assessment of the mapping results. Easymap is available at http://genetics.edu.umh.es/resources/easymap; its Quickstart Installation Guide details the recommended procedure for installation.https://www.frontiersin.org/articles/10.3389/fpls.2021.655286/fullbioinformaticsNGSmapping-by-sequencingcandidate mutationsforward geneticslinkage analysis mapping
collection DOAJ
language English
format Article
sources DOAJ
author Samuel Daniel Lup
David Wilson-Sánchez
Sergio Andreu-Sánchez
José Luis Micol
spellingShingle Samuel Daniel Lup
David Wilson-Sánchez
Sergio Andreu-Sánchez
José Luis Micol
Easymap: A User-Friendly Software Package for Rapid Mapping-by-Sequencing of Point Mutations and Large Insertions
Frontiers in Plant Science
bioinformatics
NGS
mapping-by-sequencing
candidate mutations
forward genetics
linkage analysis mapping
author_facet Samuel Daniel Lup
David Wilson-Sánchez
Sergio Andreu-Sánchez
José Luis Micol
author_sort Samuel Daniel Lup
title Easymap: A User-Friendly Software Package for Rapid Mapping-by-Sequencing of Point Mutations and Large Insertions
title_short Easymap: A User-Friendly Software Package for Rapid Mapping-by-Sequencing of Point Mutations and Large Insertions
title_full Easymap: A User-Friendly Software Package for Rapid Mapping-by-Sequencing of Point Mutations and Large Insertions
title_fullStr Easymap: A User-Friendly Software Package for Rapid Mapping-by-Sequencing of Point Mutations and Large Insertions
title_full_unstemmed Easymap: A User-Friendly Software Package for Rapid Mapping-by-Sequencing of Point Mutations and Large Insertions
title_sort easymap: a user-friendly software package for rapid mapping-by-sequencing of point mutations and large insertions
publisher Frontiers Media S.A.
series Frontiers in Plant Science
issn 1664-462X
publishDate 2021-05-01
description Mapping-by-sequencing strategies combine next-generation sequencing (NGS) with classical linkage analysis, allowing rapid identification of the causal mutations of the phenotypes exhibited by mutants isolated in a genetic screen. Computer programs that analyze NGS data obtained from a mapping population of individuals derived from a mutant of interest to identify a causal mutation are available; however, the installation and usage of such programs requires bioinformatic skills, modifying or combining pieces of existing software, or purchasing licenses. To ease this process, we developed Easymap, an open-source program that simplifies the data analysis workflows from raw NGS reads to candidate mutations. Easymap can perform bulked segregant mapping of point mutations induced by ethyl methanesulfonate (EMS) with DNA-seq or RNA-seq datasets, as well as tagged-sequence mapping for large insertions, such as transposons or T-DNAs. The mapping analyses implemented in Easymap have been validated with experimental and simulated datasets from different plant and animal model species. Easymap was designed to be accessible to all users regardless of their bioinformatics skills by implementing a user-friendly graphical interface, a simple universal installation script, and detailed mapping reports, including informative images and complementary data for assessment of the mapping results. Easymap is available at http://genetics.edu.umh.es/resources/easymap; its Quickstart Installation Guide details the recommended procedure for installation.
topic bioinformatics
NGS
mapping-by-sequencing
candidate mutations
forward genetics
linkage analysis mapping
url https://www.frontiersin.org/articles/10.3389/fpls.2021.655286/full
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