<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>RNA-seq of coding RNA</study_type><organism>Arabidopsis thaliana</organism><species>Arabidopsis thaliana</species><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-14268</full_dataset_link><description>Floral buds at meiotic stage from Col, h2a.w7, cmt3 and h2a.w7 cmt3 Arabidopsis thaliana plants were extracted as previously described (Lambing at al, 2020 Plant Cell - PMID: 32024691), and cDNA used to produce libraries.</description><repository>biostudies-arrayexpress</repository><sample_protocol>Nucleic Acid Extraction - 100 mg of unopened flower buds was ground in liquid nitrogen and RNA was extracted using TRIzol reagent.</sample_protocol><sample_protocol>Library Construction - Six micrograms of total RNA per sample was treated with DNase I. Four micrograms of total DNase I–treated total RNA was then treated with Ribo-Zero rRNA Removal Kit (MRZPL116, Epicentre) to deplete rRNA from the RNA sample. Fifty nanograms of rRNA-depleted DNase I–treated RNA was used to prepare RNA-seq libraries using the ScriptSeq v2 RNA-seq Library Preparation Kit (SSV21124, Epicentre)</sample_protocol><sample_protocol>Growth Protocol - Plants were grown under long day conditions (16 hours light/8 hours dark) at 20°C.</sample_protocol><sample_protocol>Sequencing - RNA-seq libraries were sequenced on an Illumina NextSeq 500 instrument to generate paired-end (2×76 bp) reads.</sample_protocol><sample_protocol>Sample Collection - Unopened flower buds at floral stage 9 were collected in tubes, snap frozen in liquid nitrogen and stored at -80°C until further use.</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>RNA-seq of Col, h2a.w7, cmt3 and h2a.w7 cmt3 Arabidopsis thaliana floral buds</name><description>Floral buds at meiotic stage from Col, h2a.w7, cmt3 and h2a.w7 cmt3 Arabidopsis thaliana plants were extracted as previously described (Lambing at al, 2020 Plant Cell - PMID: 32024691), and cDNA used to produce libraries.</description><dates><release>2025-07-13T00:00:00Z</release><modification>2024-07-22T10:16:40.461Z</modification><creation>2024-07-22T10:16:40.461Z</creation></dates><accession>E-MTAB-14268</accession><cross_references><ENA>ERP162183</ENA><Biostudies>E-MTAB-7371</Biostudies><EFO>EFO_0002944</EFO><EFO>EFO_0004170</EFO><EFO>EFO_0003789</EFO><EFO>EFO_0005518</EFO><EFO>EFO_0003738</EFO><EFO>EFO_0004184</EFO></cross_references></HashMap>