<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/SRR279/014/SRR27918914/SRR27918914_1.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR279/018/SRR27918918/SRR27918918_1.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR279/020/SRR27918920/SRR27918920_1.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR279/016/SRR27918916/SRR27918916_2.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR279/020/SRR27918920/SRR27918920_2.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR279/013/SRR27918913/SRR27918913_2.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR279/018/SRR27918918/SRR27918918_2.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR279/014/SRR27918914/SRR27918914_2.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR279/016/SRR27918916/SRR27918916_1.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR279/013/SRR27918913/SRR27918913_1.fastq.gz</Fastqsanger.gz><Other>ftp://</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Genomics</omics_type><center_name>Adelaide Centre for Epigenetics and the South Australian Immunogenomics Cancer Institute, Faculty of Health and Medical Sciences, The University of Adelaide</center_name><full_dataset_link>https://www.ebi.ac.uk/ena/browser/view/PRJNA1074726</full_dataset_link><scientific_name>Homo sapiens</scientific_name><long_description>In this study, we wanted to study the changes in the NK cell transcriptome after culturing in the presence of IL-15 and TGF-beta by using single cell RNA sequencing (sc-RNAseq) Overall design: Peripheral blood mononuclear cells were collected from a healthy donor and cultured in the presence of IL-15+TGF-beta or non-stimulus. Cells were cultured for 1 and 4 days. Next, sc-RNAseq was performed using Illumina Novaseq 6000.</long_description><tag>xref:PubMed:40437214</tag><repository>ENA</repository></additional><is_claimable>false</is_claimable><name>Activated NK cells with a predominance of inhibitory receptors and a decidual-like phenotype expand after autologous HSCT in children with tumors</name><description>Activated NK cells with a predominance of inhibitory receptors and a decidual-like phenotype expand after autologous HSCT in children with tumors</description><dates><last_updated>2025-09-24</last_updated><first_public>2025-06-07</first_public></dates><accession>PRJNA1074726</accession><cross_references><GEO>GSE255347</GEO><taxon>9606</taxon><PubMed>40437214</PubMed></cross_references></HashMap>