<HashMap><database>ENA</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR115/026/SRR11550226/SRR11550226.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR115/022/SRR11550222/SRR11550222.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR115/027/SRR11550227/SRR11550227.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR115/023/SRR11550223/SRR11550223.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR115/030/SRR11550230/SRR11550230.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR115/025/SRR11550225/SRR11550225.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR115/028/SRR11550228/SRR11550228.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR115/020/SRR11550220/SRR11550220.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR115/024/SRR11550224/SRR11550224.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR115/031/SRR11550231/SRR11550231.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR115/029/SRR11550229/SRR11550229.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR115/021/SRR11550221/SRR11550221.fastq.gz</Fastqsanger.gz></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Genomics</omics_type><center_name>Bioinformatics Core, MDI Biological Laboratory</center_name><full_dataset_link>https://www.ebi.ac.uk/ena/browser/view/PRJNA625528</full_dataset_link><scientific_name>Caenorhabditis elegans</scientific_name><tag>xref:PubMed:36273621</tag><tag>xref:EuropePMC:PMC9677334</tag><long_description>This experiment compares gene expression and polysome profiling between a strain where glh-1 is present - DUP64 glh-1(sam24[glh-1::gfp::3xFlag]) I and a strain where the glh-1 coding sequence has been deleted DUP144 glh-1(sam65[Δglh-1::gfp::3xFlag]) I Overall design: For each of three replicates, 25 plates of each strain were used to inoculate 1L of S Media containing 5 grams of freeze-dried OP50 (LabTie, Leiden, The Netherlands). Liquid cultures were incubated in 4 1L beveled flasks at 20° C until worms were gravid, at which point embryos were harvested, washed, bleach-treated (Montserrat et al. 2012) and hatched overnight. The synchronized L1-staged worms were used to inoculate another 1L of S Media with OP50 and were grown for approximately 40 hours until the majority reached the young adult stage, where they were harvested, washed, pelleted and flash frozen in 1-ml aliquots.</long_description><repository>ENA</repository></additional><is_claimable>false</is_claimable><name>Analysis of gene expression and polysome profiling in the presence and absence of glh-1 in C. Elegans</name><description>Analysis of gene expression and polysome profiling in the presence and absence of glh-1 in C. Elegans</description><dates><last_updated>2025-09-24</last_updated><first_public>2022-11-24</first_public></dates><accession>PRJNA625528</accession><cross_references><GEO>GSE148737</GEO><taxon>6239</taxon><PubMed>36273621</PubMed></cross_references></HashMap>