<HashMap><database>biostudies-arrayexpress</database><scores/><additional><submitter>David Toppe</submitter><organism>Drosophila melanogaster</organism><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-17037</full_dataset_link><description>This Dataset contains global mRNA expression data of 10 day old female adult Drosophila melanogaster heads in which autophagy, a fundamental cellular degradation pathway in contexts of health and disease, is impaired in a major brain region, the Mushroombody, by RNAi mediated knockdown of Atg5 (ok107-Gal4>UAS-Atg5-RNAi). The control group consists of an age- and sex-matched wildtypic Drosophila strain (ok107-Gal4/+).  4 biological replicates per genotype were processed, each sample containing around 50 Drosophila heads. Samples labelled with AB1-AB4 refer to the control group, samples labelled with XY1-XY4 to the Atg5 knockdown group.</description><repository>biostudies-arrayexpress</repository><sample_protocol>Library Construction - Nucleic acid library construction was performed by Lexogen using the QuantSeq method.</sample_protocol><sample_protocol>Nucleic Acid Extraction - Nucleic acid extraction was performed by Lexogen using the QuantSeq method.</sample_protocol><sample_protocol>Sequencing - Nucleic acid sequencing was performed by Lexogen using the QuantSeq method.</sample_protocol><sample_protocol>Sample Collection - Adult Drosophila female flies, raised for 10 days at 29°C, were snap-frozen in liquid nitrogen and stored at -80 degrees until sample collection of all biological replicates was completed. Flies were subsequently decapitated mechanically and fly heads were again stored at -80 degrees. Samples were shipped on dry ice for further processing by Lexogen.</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>Data Transformation - Reads were aligned to a reference genome with STAR aligner. The differential expression analysis was performed with the DeSeq2 bioconducter package by Lexogen</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 iSeq 100</instrument_platform><study_type>RNA-seq of coding RNA</study_type><species>Drosophila melanogaster</species><pubmed_authors>David Toppe</pubmed_authors></additional><is_claimable>false</is_claimable><name>RNA Seq Data of adult Drosophila melanogaster heads with Mushroombody-specific knockdown of Atg5 in comparison to wildtype controls</name><description>This Dataset contains global mRNA expression data of 10 day old female adult Drosophila melanogaster heads in which autophagy, a fundamental cellular degradation pathway in contexts of health and disease, is impaired in a major brain region, the Mushroombody, by RNAi mediated knockdown of Atg5 (ok107-Gal4>UAS-Atg5-RNAi). The control group consists of an age- and sex-matched wildtypic Drosophila strain (ok107-Gal4/+).  4 biological replicates per genotype were processed, each sample containing around 50 Drosophila heads. Samples labelled with AB1-AB4 refer to the control group, samples labelled with XY1-XY4 to the Atg5 knockdown group.</description><dates><release>2026-06-30T00:00:00Z</release><modification>2026-06-30T01:01:10.303Z</modification><creation>2026-05-14T12:23:00.364Z</creation></dates><accession>E-MTAB-17037</accession><cross_references><ENA>ERP193432</ENA><EFO>EFO_0002944</EFO><EFO>EFO_0004170</EFO><EFO>EFO_0005518</EFO><EFO>EFO_0003816</EFO><EFO>EFO_0003738</EFO><EFO>EFO_0004184</EFO></cross_references></HashMap>