<HashMap><database>biostudies-other</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Urs Mörbe</submitter><funding>Novo Nordisk Foundation</funding><funding>European Crohn’s and Colitis Organisation </funding><funding>Lundbeck Foundation</funding><funding>Louis-Hansen-Foundation</funding><species>Homo sapiens (human)</species><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-BSST2281</full_dataset_link><repository>biostudies-other</repository><funding_grant_id>R155-2014-4184</funding_grant_id><funding_grant_id>NNF22OC0071681</funding_grant_id><pubmed_authors>Urs Mörbe</pubmed_authors></additional><is_claimable>false</is_claimable><name>Fibroblast diversity within human gut-associated lymphoid tissues</name><description>The provided data include the scRNA-seq data and flow cytometry metadata of the study entitled "Fibroblast diversity within human gut-associated lymphoid tissues", published in the Journal of Experimental Medicine.

Procedure for scRNA-seq: 
Input: Resection material of patients undergoing surgery for colorectal cancer (healthy controls, samples  taken >10cm from tumour site and macroscopically tumour free) or IBD resections from the distal ileum. Samples were processed to obtain single cell suspensions as described by Jørgensen et al. (PMID: 33619391). Cells were sorted on a BD Aria cell sorter. After sorting, the cells were subjected to single cell RNA-sequencing using the 10x Genomics platform.

scRNA-seq data is provided as read count matrices as well as FASTQ files that were anonymized using the BAMboozled pipeline (PMID: 34711808). FASTQ files: In short, patient identifiable information such as SNPs, insertions and deletions were replaced with the information of the human reference genome to remove person-identifiable information.  
</description><dates><release>2025-11-21T00:00:00Z</release><modification>2026-04-16T19:52:35.52Z</modification><creation>2025-11-14T13:27:43.975Z</creation></dates><accession>S-BSST2281</accession><cross_references/></HashMap>