<HashMap><database>biostudies-arrayexpress</database><scores/><additional><submitter>Yu Pengjie</submitter><organism>Homo sapiens</organism><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-16200</full_dataset_link><description>The evaluation of RNA-binding proteins (RBPs) is based on their RNA-binding capacity and the yield of protein recovered in assays. To determine the specificity of ZFP36's RNA interactions in AGS cells, we performed iRIP-seq to identify its directly bound mRNA targets.</description><repository>biostudies-arrayexpress</repository><sample_protocol>Nucleic Acid Extraction - The GENE-bound RNA was isolated from the immunoprecipitation of anti-GENE using Trizol (Invitrogen).</sample_protocol><sample_protocol>Library Construction - Complementary DNA (cDNA) libraries were prepared with the KAPA RNA Hyper Prep Kit (KAPA, KK8541) according to the manufacturer’s procedure</sample_protocol><sample_protocol>Sequencing - Illumina NovaSeq 6000 system was used for 150 nt paired-end sequencing.</sample_protocol><sample_protocol>Sample Collection - Jurkat and Molt4 cells were grown at 37℃, 5% CO2 in RPMI-1640 medium (Gibco, USA) supplemented with 10% fetal bovine serum (FBS, Gibco, USA) and 1% penicillin/streptomycin, respectively.</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 - After reads were aligned onto the genome, we analysed the unique reads binding regions of GENE_NAME on genome using “ABLIRC” strategy.</data_protocol><data_protocol>Sequence Alignment - Raw sequencing reads containing more than 2-N bases were first discarded. Subsequently, the raw reads were trimmed of adaptors and low-quality bases using a FASTX-Toolkit (v.0.0.13; http://hannonlab.cshl.edu/fastx toolkit/).  In addition, short reads of less than 16 nt were dropped to retain clean reads, which were subsequently aligned to the GRch38 genome by HISAT2</data_protocol><omics_type>Unknown</omics_type><omics_type>Transcriptomics</omics_type><omics_type>Genomics</omics_type><omics_type>Proteomics</omics_type><instrument_platform>Illumina NovaSeq 6000</instrument_platform><study_type>RIP-seq</study_type><species>Homo sapiens</species><pubmed_authors>Yu Pengjie</pubmed_authors></additional><is_claimable>false</is_claimable><name>ZFP36 Inhibits Gastric Cancer Progression by enhancing expression of LIPG and binding its 3’UTR of RNA</name><description>The evaluation of RNA-binding proteins (RBPs) is based on their RNA-binding capacity and the yield of protein recovered in assays. To determine the specificity of ZFP36's RNA interactions in AGS cells, we performed iRIP-seq to identify its directly bound mRNA targets.</description><dates><release>2025-12-11T00:00:00Z</release><modification>2025-12-11T02:01:55.203Z</modification><creation>2025-11-19T19:04:56.946Z</creation></dates><accession>E-MTAB-16200</accession><cross_references><ENA>ERP185352</ENA><EFO>EFO_0002944</EFO><EFO>EFO_0004170</EFO><EFO>EFO_0005310</EFO><EFO>EFO_0004917</EFO><EFO>EFO_0005518</EFO><EFO>EFO_0003816</EFO><EFO>EFO_0004184</EFO></cross_references></HashMap>