<HashMap><database>biostudies-arrayexpress</database><scores/><additional><submitter>Keiichi Mochida</submitter><organism>Euglena agilis</organism><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-7293</full_dataset_link><description>To analyze the transcriptome after heat stress in Euglena agilis,  we analyzed a series of RNA-seq data from E. agilis cells grown under control (23°C) and heat stress (35°C) conditions at 2 time-points (at 8 and 24 h of heat stress exposure).</description><repository>biostudies-arrayexpress</repository><sample_protocol>Sample Treatment - We cultured E. agilis in mAC media at 23°C for more than 3 days and transferred the cells to a temperature of 35°C and incubated them for 8 and 24 h for mRNA preparation.</sample_protocol><sample_protocol>Sample Collection - The culture was maintained in 100-mL test tubes containing 50 mL of media with aeration (50 mL/min) and constant illumination (100 μmol photon/m2s) in four biological replicates.</sample_protocol><sample_protocol>Nucleic Acid Extraction - Total RNA was extracted from the cells cultured at 23°C (control) and 35°C for 8 and 24 h using NucleoSpin RNA (Macherey-Nagel).</sample_protocol><sample_protocol>Growth Protocol - We cultured E. agilis in mAC media at 23°C for more than 3 days and transferred the cells to a temperature of 35°C and incubated them for 8 and 24 h for mRNA preparation.</sample_protocol><sample_protocol>Library Construction - Sequencing libraries were constructed using a TruSeq Stranded mRNA Sample Preparation Kit (Illumina, Inc.).</sample_protocol><sample_protocol>Sequencing - The sequencing libraries were sequenced using a Hiseq 4000 with a TruSeq SBS Kit v2 – HS (Illumina, Inc.) by the paired-end sequencing method for sequences 100 bp in length.</sample_protocol><figure_sub>Organization</figure_sub><figure_sub>MINSEQE Score</figure_sub><figure_sub>Assays and Data</figure_sub><figure_sub>Processed Data</figure_sub><figure_sub>MAGE-TAB Files</figure_sub><data_protocol>Sequence Alignment - The quality-checked transcriptome sequencing reads from the heat stress treated cells of E. agilis, were mapped to the E. agilis genome using HISAT2 (ver. 2.0.5) with the parameter setting of --pen-noncansplice = 0 -no-softclip.</data_protocol><data_protocol>Data Transformation - Normalized read counts for the E. agilis genes were computed by using the featureCounts program (v. 1.5.0-p3) with default parameters.</data_protocol><omics_type>Metabolomics</omics_type><omics_type>Unknown</omics_type><omics_type>Transcriptomics</omics_type><omics_type>Genomics</omics_type><omics_type>Proteomics</omics_type><instrument_platform>Illumina HiSeq 4000</instrument_platform><study_type>RNA-seq of coding RNA</study_type><species>Euglena agilis</species><pubmed_authors>Keiichi Mochida</pubmed_authors></additional><is_claimable>false</is_claimable><name>Heat stress transcriptome analysis in Euglena agilis</name><description>To analyze the transcriptome after heat stress in Euglena agilis,  we analyzed a series of RNA-seq data from E. agilis cells grown under control (23°C) and heat stress (35°C) conditions at 2 time-points (at 8 and 24 h of heat stress exposure).</description><dates><release>2025-09-01T00:00:00Z</release><modification>2025-09-01T01:02:25.111Z</modification><creation>2022-01-28T21:38:51.068Z</creation></dates><accession>E-MTAB-7293</accession><cross_references><ENA>ERP111434</ENA><EFO>EFO_0002944</EFO><EFO>EFO_0004170</EFO><EFO>EFO_0003789</EFO><EFO>EFO_0004917</EFO><EFO>EFO_0003816</EFO><EFO>EFO_0005518</EFO><EFO>EFO_0003738</EFO><EFO>EFO_0004184</EFO><EFO>EFO_0003969</EFO></cross_references></HashMap>