<HashMap><database>biostudies-arrayexpress</database><scores/><additional><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><submitter>Andreas Bikfalvi</submitter><instrument_platform>Illumina NovaSeq 6000</instrument_platform><study_type>single nucleus RNA sequencing</study_type><organism>Mus musculus</organism><species>Mus musculus</species><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-14432</full_dataset_link><description>Murine renal carcinoma RENCA cells were injected in BALB/c mice to generated either primary tumours (orthotopically) or lunge metastases (through tail vein injection, or directly forming from primary tumors). Samples were snap-frozen and processed for single nucleus isolation and RNA seq analysis. Tumor cells expressed Interleukin-34 (IL34-OE) or an empty vector as control (Ctrl). The goal is to finely dissect tumor microenvironmental changes occurring in an IL34-enriched tumor microenvironment, either in primary tumors or lung metastases.</description><repository>biostudies-arrayexpress</repository><sample_protocol>Sample Collection - Fresh samples were quick-frozen in liquid nitrogen and stored at -80°C until the day of nuclei isolation</sample_protocol><sample_protocol>Library Construction - 17,000 nuclei/sample were processed for Gel Bead-in-Emulsion (GEM) and library generation using Chromium Next GEM Single Cell 3’ GEM, Library &amp; Gel Bead Kit v3.1 (10X Genomics)</sample_protocol><sample_protocol>Sequencing - The libraries were sequenced using an Illumina NovaSeq 6000</sample_protocol><sample_protocol>Nucleic Acid Extraction - Frozen samples were dounce-homogenized in ice-cold Lysis Buffer containing 0.1% TritonX</sample_protocol><figure_sub>Organization</figure_sub><figure_sub>MINSEQE Score</figure_sub><figure_sub>Assays and Data</figure_sub><figure_sub>MAGE-TAB Files</figure_sub><pubmed_authors>Andreas Bikfalvi</pubmed_authors><pubmed_authors>Andrea Emanuelli</pubmed_authors></additional><is_claimable>false</is_claimable><name>Single-nucleus RNA seq of murine renal tumors and lung metastases generated by RENCA cells overexpressing Interleukin-34</name><description>Murine renal carcinoma RENCA cells were injected in BALB/c mice to generated either primary tumours (orthotopically) or lunge metastases (through tail vein injection, or directly forming from primary tumors). Samples were snap-frozen and processed for single nucleus isolation and RNA seq analysis. Tumor cells expressed Interleukin-34 (IL34-OE) or an empty vector as control (Ctrl). The goal is to finely dissect tumor microenvironmental changes occurring in an IL34-enriched tumor microenvironment, either in primary tumors or lung metastases.</description><dates><release>2025-06-10T00:00:00Z</release><modification>2025-06-10T10:00:49.02Z</modification><creation>2024-09-06T12:21:42.388Z</creation></dates><accession>E-MTAB-14432</accession><cross_references><ENA>ERP163889</ENA><EFO>EFO_0002944</EFO><EFO>EFO_0004170</EFO><EFO>EFO_0009809</EFO><EFO>EFO_0005518</EFO><EFO>EFO_0004184</EFO></cross_references></HashMap>