<HashMap><database>ENA</database><scores/><additional><omics_type>Genomics</omics_type><center_name>Institute of Molecular Biology gGmbH, Mainz</center_name><center_name>Rene Ketting group</center_name><full_dataset_link>https://www.ebi.ac.uk/ena/browser/view/PRJEB95103</full_dataset_link><long_description>We carried out small RNA sequencing in different C. elegans strains with mutations of the WAGO-1 and WAGO-3 IDR processing proteases app-1 and dpf-3. Additionally, we carried out RNA immunoprecipitation sequencing (RIP-Seq) of tagged versions of WAGO-1 and WAGO-3 with or without deletions to their IDRs. Because deletion of either IDR is lethal, but full deletions of the proteins are not, all strains used for RIP-Seq carried and auxin-inducible degron and were grown on auxin plates until 4 hours before harvest. All sequencing libraries were treated with RppH to enrich for 22G RNAs.</long_description><repository>ENA</repository></additional><is_claimable>false</is_claimable><name>WAGO-1/3 IDR processing</name><description>Effects of IDR processing in WAGO-1 and WAGO-3 on small RNA binding and overall small RNA landscapes</description><dates><last_updated>2025-08-06</last_updated><first_public>2025-08-06</first_public></dates><accession>PRJEB95103</accession><cross_references/></HashMap>