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.  

Supplementary analysis of snRNAseq data in the manuscript:

Novel ARPKD mouse model with near complete deletion of Polycystic Kidney and Hepatic Disease 1 (Pkhd1) genomic locus has multiple phenotypes but no renal cysts

Authors:

Yu Ishimoto1,5, Luis F Menezes1,5,6, Fang Zhou1, Teruhiko Yoshida1, Taishi Komori2, Jiahe Qiu1, Marian F Young2, Huiyan Lu3, Svetlana Potapova3, Patricia Outeda4, Terry Watnick4, Gregory G Germino1, 6.

Affiliations:

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.