{"database":"ENA","file_versions":[],"scores":null,"additional":{"omics_type":["Genomics"],"center_name":["Institute of Molecular Biology gGmbH, Mainz","Rene Ketting group"],"full_dataset_link":["https://www.ebi.ac.uk/ena/browser/view/PRJEB95103"],"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."],"repository":["ENA"],"additional_accession":[]},"is_claimable":false,"name":"WAGO-1/3 IDR processing","description":"Effects of IDR processing in WAGO-1 and WAGO-3 on small RNA binding and overall small RNA landscapes","dates":{"last_updated":"2025-08-06","first_public":"2025-08-06"},"accession":"PRJEB95103","cross_references":{}}