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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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 |
work_keys_str_mv |
AT samueldaniellup easymapauserfriendlysoftwarepackageforrapidmappingbysequencingofpointmutationsandlargeinsertions AT davidwilsonsanchez easymapauserfriendlysoftwarepackageforrapidmappingbysequencingofpointmutationsandlargeinsertions AT sergioandreusanchez easymapauserfriendlysoftwarepackageforrapidmappingbysequencingofpointmutationsandlargeinsertions AT joseluismicol easymapauserfriendlysoftwarepackageforrapidmappingbysequencingofpointmutationsandlargeinsertions |
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