<HashMap><database>ENA</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR223/055/SRR22355255/SRR22355255.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR223/056/SRR22355256/SRR22355256.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR223/053/SRR22355253/SRR22355253.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR223/054/SRR22355254/SRR22355254.fastq.gz</Fastqsanger.gz></files><type>primary</type></body><statusCodeValue>200</statusCodeValue><statusCode>OK</statusCode></file_versions><scores/><additional><omics_type>Genomics</omics_type><center_name>Liver Cancer Institute, Department of Liver Surgery and Transplantation, Liver Cancer Institute, Zhongshan Hospital Fudan University</center_name><full_dataset_link>https://www.ebi.ac.uk/ena/browser/view/PRJNA903800</full_dataset_link><scientific_name>Mus musculus</scientific_name><long_description>To understand how SIGLEC15 regulates CD8+ T cells in tumor microenvironment, we enriched CD8+ T cells using magnetic beads after tumor digestion. Collected CD8+ T cells were examined with flowcytometry analysis and were further loaded for sequencing analysis. Overall design: IgG (n=6) and anti-SIGLEC15 (n=6) treated percutaneous tumor grafts were constructed in C57 mice and collected in day19 after 2 weeks of intraperitoneal injection. Collected CD8+ T cells were stained for further examination in flowcytometry analysis. After confirmation, 3 samples of collected cell pelletes were mixed together and loaded for sequencing analysis.</long_description><tag>xref:PubMed:38988824</tag><repository>ENA</repository><description_synonyms>Cancer Microenvironments, Thymus-Dependent Lymphocytes, Microenvironment, T-Cells, p32, Thymus-Dependent, Leu2, T, Lymphocytes, RNA-seq., T-Lymphocyte, Tumor, Dietary Fiber, Cell, Thymus-Dependent Lymphocyte, T Cells, T Lymphocyte, T-Cell, Cancer Microenvironment, Cells, Whole Transcriptome Shotgun Sequencing, T Cell, CD8, Tumor Microenvironments, MAL, T Lymphocytes, Microenvironments, Thymus Dependent Lymphocytes, Lymphocyte, Cancer</description_synonyms><name_synonyms>Cancer Microenvironments, Thymus-Dependent Lymphocytes, Microenvironment, T-Cells, p32, Thymus-Dependent, Leu2, T, Lymphocytes, RNA-seq., T-Lymphocyte, Tumor, Dietary Fiber, Cell, Thymus-Dependent Lymphocyte, T Cells, T Lymphocyte, T-Cell, Cancer Microenvironment, Cells, Whole Transcriptome Shotgun Sequencing, T Cell, CD8, Tumor Microenvironments, MAL, T Lymphocytes, Microenvironments, Thymus Dependent Lymphocytes, Lymphocyte, Cancer</name_synonyms></additional><is_claimable>false</is_claimable><name>Functional Changes of CD8+ T Cells in Tumor Microenvironment after SIGLEC15 Blockade [bulk RNA-seq]</name><description>Functional Changes of CD8+ T Cells in Tumor Microenvironment after SIGLEC15 Blockade [bulk RNA-seq]</description><dates><last_updated>2025-09-24</last_updated><first_public>2024-08-10</first_public></dates><accession>PRJNA903800</accession><cross_references><GEO>GSE218409</GEO><taxon>10090</taxon><PubMed>38988824</PubMed></cross_references></HashMap>