<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Lup SD</submitter><funding>Ministerio de Ciencia e Innovación</funding><funding>Generalitat Valenciana</funding><pagination>1042913</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9909543</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>14</volume><pubmed_abstract>Mapping-by-sequencing combines Next Generation Sequencing (NGS) with classical genetic mapping by linkage analysis to establish gene-to-phenotype relationships. Although numerous tools have been developed to analyze NGS datasets, only a few are available for mapping-by-sequencing. One such tool is Easymap, a versatile, easy-to-use package that performs automated mapping of point mutations and large DNA insertions. Here, we describe Easymap v.2, which also maps small insertion/deletions (InDels), and includes workflows to perform QTL-seq and variant density mapping analyses. Each mapping workflow can accommodate different experimental designs, including outcrossing and backcrossing, F&lt;sub>2&lt;/sub>, M&lt;sub>2&lt;/sub>, and M&lt;sub>3&lt;/sub> mapping populations, chemically induced mutation and natural </pubmed_abstract><journal>Frontiers in plant science</journal><pubmed_title>Versatile mapping-by-sequencing with Easymap v.2.</pubmed_title><pmcid>PMC9909543</pmcid><funding_grant_id>PROMETEO/2019/117, ACIF/2018/005</funding_grant_id><funding_grant_id>PGC2018-093445-B-I00, PID2021-127725NB-I00</funding_grant_id><pubmed_authors>Micol JL</pubmed_authors><pubmed_authors>Navarro-Quiles C</pubmed_authors><pubmed_authors>Lup SD</pubmed_authors></additional><is_claimable>false</is_claimable><name>Versatile mapping-by-sequencing with Easymap v.2.</name><description>Mapping-by-sequencing combines Next Generation Sequencing (NGS) with classical genetic mapping by linkage analysis to establish gene-to-phenotype relationships. Although numerous tools have been developed to analyze NGS datasets, only a few are available for mapping-by-sequencing. One such tool is Easymap, a versatile, easy-to-use package that performs automated mapping of point mutations and large DNA insertions. Here, we describe Easymap v.2, which also maps small insertion/deletions (InDels), and includes workflows to perform QTL-seq and variant density mapping analyses. Each mapping workflow can accommodate different experimental designs, including outcrossing and backcrossing, F&lt;sub>2&lt;/sub>, M&lt;sub>2&lt;/sub>, and M&lt;sub>3&lt;/sub> mapping populations, chemically induced mutation and natural </description><dates><release>2023-01-01T00:00:00Z</release><publication>2023</publication><modification>2026-07-14T18:40:42.766Z</modification><creation>2024-11-09T01:30:26.794Z</creation></dates><accession>S-EPMC9909543</accession><cross_references><pubmed>36778692</pubmed><doi>10.3389/fpls.2023.1042913</doi></cross_references></HashMap>