10x BPH sequencing on all cells

Single-cell mRNA sequencing (scRNA-seq) study was conducted to to probe heterogeneity of human BPH associated cells. No cell sorting was conducted so all cells within the BPH environment could be represented. Overall design: Human BPH tissues were mechanically and enzymatically digested, then debris removed using the Debris Removal Solution (Miltenyi). scRNA-seq was performed for all 5 samples, and 4 out of 5 samples have CITE-seq (cell surface protein expression) data Please note that the processed data was generated from both CSP and cDNA samples combined (except the '047563_1562-all-cells' sample) and is linked to the corresponding *_cDNA sample records.