<HashMap><database>biostudies-arrayexpress</database><scores/><additional><omics_type>Unknown</omics_type><omics_type>Transcriptomics</omics_type><omics_type>Genomics</omics_type><omics_type>Proteomics</omics_type><submitter>Christophe Lambing</submitter><instrument_platform>NextSeq 500</instrument_platform><study_type>genotyping by high throughput sequencing</study_type><organism>Arabidopsis thaliana</organism><species>Arabidopsis thaliana</species><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-15040</full_dataset_link><description>Genomic DNA from 144 h2a.w7 Col-0 x Ler F2 individuals was extracted using CTAB (as described in Kuo et al, 2022 Methods Mol Biol - PMID: 35461443) and used to generate sequencing libraries as described (Lawrence et al, 2019 Current Biology - PMID: 31378616). Sequencing data was analysed to identify crossovers using the TIGER pipeline as previously described (Rowan et al, 2015 G3 (Bethesda) - PMID: 25585881; Yelina et al, 2015 Genes &amp; Dev - PMID: 26494791; Lawrence et al, 2019 Current Biology - PMID: 31378616).</description><repository>biostudies-arrayexpress</repository><sample_protocol>Growth Protocol - Plant were grown in growth chambers under the following conditions: 60% humidity, long day conditions (16 hours light/ 8 hours dark) at 20oC.</sample_protocol><sample_protocol>Nucleic Acid Extraction - DNA was extracted using CTAB procedure as previously described (Kuo et al, 2022 Methods Mol Biol - PMID: 35461443)</sample_protocol><sample_protocol>Sample Collection - Leaf tissue at rosette stage were collected from 5-week old plants. Plant tissue was immediately snap frozen in liquid nitrogen and stored at -80oC.</sample_protocol><sample_protocol>Library Construction - DNA library preparation was prepared as previously described (Lawrence et al, 2019 Current Biology - PMID: 31378616) – TruSeq DNA sample prep kit. Illumina sequencing</sample_protocol><sample_protocol>Sequencing - Libraries were subjected to paired-end sequenced using an Illumina Genome Analyzer. Illumina NextSeq500 instrument.</sample_protocol><figure_sub>Organization</figure_sub><figure_sub>MINSEQE Score</figure_sub><figure_sub>Assays and Data</figure_sub><figure_sub>MAGE-TAB Files</figure_sub><pubmed_authors>Christophe Lambing</pubmed_authors></additional><is_claimable>false</is_claimable><name>Identifying crossover locations in Arabidopsis thaliana h2a.w7 Col-0 × Ler F2 populations using genotyping-by-sequencing</name><description>Genomic DNA from 144 h2a.w7 Col-0 x Ler F2 individuals was extracted using CTAB (as described in Kuo et al, 2022 Methods Mol Biol - PMID: 35461443) and used to generate sequencing libraries as described (Lawrence et al, 2019 Current Biology - PMID: 31378616). Sequencing data was analysed to identify crossovers using the TIGER pipeline as previously described (Rowan et al, 2015 G3 (Bethesda) - PMID: 25585881; Yelina et al, 2015 Genes &amp; Dev - PMID: 26494791; Lawrence et al, 2019 Current Biology - PMID: 31378616).</description><dates><release>2025-07-11T00:00:00Z</release><modification>2025-04-10T10:27:11.885Z</modification><creation>2025-04-10T10:27:11.885Z</creation></dates><accession>E-MTAB-15040</accession><cross_references><ENA>ERP171467</ENA><Biostudies>E-MTAB-8725</Biostudies><EFO>EFO_0002944</EFO><EFO>EFO_0004170</EFO><EFO>EFO_0003789</EFO><EFO>EFO_0002771</EFO><EFO>EFO_0005518</EFO><EFO>EFO_0004184</EFO></cross_references></HashMap>