<HashMap><database>biostudies-arrayexpress</database><scores/><additional><submitter>Jeffrey Ishizuka</submitter><organism>Homo sapiens</organism><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-15926</full_dataset_link><description>MCC13 MDK-WT and MDK-KO tumor cells were treated with IFNb for 24 hours and underwent bulk RNAseq. There are in total 4 conditions (control + no stim, control + IFNb, MDK-KO + no stim, MDK-KO + IFNb) and each condition has 3 biological replicates (except for control + no stim condition, due to poor quality, it only has two biological replicates).</description><repository>biostudies-arrayexpress</repository><sample_protocol>Sample Collection - Control and IFNb treated cells were harvested with trypsin.</sample_protocol><sample_protocol>Library Construction - 1 ug of RNA was submitted for construction of sequencing library.</sample_protocol><sample_protocol>Growth Protocol - 10x6 MCC13 MDK-WT and MDK-KO tumor cells were plated per 12-well plate of MCC13 MDK-WT and MDK-KO.</sample_protocol><sample_protocol>Nucleic Acid Extraction - RNA was harvested using Rneasy mini kit (Qiagen).</sample_protocol><sample_protocol>Sequencing - Illumina NovaSeq X Plus with 20 million read pairs per sample.</sample_protocol><sample_protocol>Sample Treatment - Cells were treated with 1000 IU/ml IFNb for 24 hours.</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 - Salmon v1.4.0 was used to quantify the reads and generate TPM and raw counts matrices.</data_protocol><data_protocol>Sequence Alignment - Raw paired-end FASTQ files were quality-checked and trimmed with fastp v0.23.2. Trimmed reads were aligned to the human genome GRCh38.p14 with Salmon v1.4.0.</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 NovaSeq X</instrument_platform><study_type>RNA-seq of coding RNA</study_type><species>Homo sapiens</species><pubmed_authors>Jeffrey Ishizuka</pubmed_authors></additional><is_claimable>false</is_claimable><name>Perturbational sequencing of patient tumors reveals midkine as an innate immune checkpoint in neuroendocrine tumors</name><description>MCC13 MDK-WT and MDK-KO tumor cells were treated with IFNb for 24 hours and underwent bulk RNAseq. There are in total 4 conditions (control + no stim, control + IFNb, MDK-KO + no stim, MDK-KO + IFNb) and each condition has 3 biological replicates (except for control + no stim condition, due to poor quality, it only has two biological replicates).</description><dates><release>2025-11-24T00:00:00Z</release><modification>2026-05-30T15:30:20.462Z</modification><creation>2025-10-29T17:04:42.521Z</creation></dates><accession>E-MTAB-15926</accession><cross_references><ENA>ERP183318</ENA><EFO>EFO_0002944</EFO><EFO>EFO_0004170</EFO><EFO>EFO_0003789</EFO><EFO>EFO_0004917</EFO><EFO>EFO_0005518</EFO><EFO>EFO_0003816</EFO><EFO>EFO_0003738</EFO><EFO>EFO_0003969</EFO><EFO>EFO_0004184</EFO></cross_references></HashMap>