Ishimoto_Pkhd1KO_kidney_snRNAseq_cellranger_outs_folder

Cellranger output from the folder filtered_feature_bc_matrix for each sample in the following manuscript. Original files with sequence data can be found in the NCBI Sequence Read Archive (SRA) archive with BioProject record PRJNA911229. <strong>Supplementary analysis of snRNAseq data in the manuscript:</strong> <strong>Novel ARPKD mouse model with near complete deletion of Polycystic Kidney and Hepatic Disease 1 (</strong><em><strong>Pkhd1</strong></em><strong>) genomic locus has multiple phenotypes but no renal cysts</strong> <strong>Authors:</strong> Yu Ishimoto^1,5, Luis F Menezes^1,5,6, Fang Zhou¹, Teruhiko Yoshida¹, Taishi Komori², Jiahe Qiu¹, Marian F Young², Huiyan Lu³, Svetlana Potapova³, Patricia Outeda⁴, Terry Watnick⁴, Gregory G Germino^{1, 6}. <strong>Affiliations:</strong> 1 Kidney Disease Branch; National Institute of Diabetes and Digestive and Kidney Disease (NIDDK), National Institutes of Health (NIH), Bethesda, Maryland, USA 2 Molecular Biology of Bones and Teeth Section, Department of Health and Human Services (DHHS), National Institutes of Dental and Craniofacial Research (NIDCR), National Institutes of Health (NIH), Bethesda, Maryland, USA 3 Mouse Transgenic Core Facility, National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), National Institutes of Health (NIH), Bethesda, MD, USA 4 University of Maryland School of Medicine, Division of Nephrology, Baltimore, Maryland, USA. 5 These authors contributed equally to the study. 6 Co-Corresponding authors.