Every cell is one point. Drag to pan, scroll to zoom, shift-drag to select a
region; click any group in the legend to isolate it. Use
Colour cells by to switch between cell type, cluster, library,
quality-control metric and the expression of a single gene.
These are the figures actually applied to the cells shown above, not the
values requested in a configuration file. Every dataset is filtered
independently; see
Single-cell Data for the full table across all
datasets.
Source BioProject
PRJNA1223412
SRA study
SRP563749
GEO series
GSE289546
Library type
10x Genomics Chromium (high confidence)
Libraries integrated
4
Cells reported by source
29723
Cells before filtering
29,723
Cells after cell filtering
21,794
Doublets removed
19 (0.09%)
Cells after filtering
21,775
Retained
73.3%
Filtering strategy
Per-library MAD outlier detection (adaptive)
Thresholds applied
adaptive: per-library MAD (5.0 MADs) on UMI, genes and MT%, floor 200 genes, floor 500 UMI
Mitochondrial genes found
0 — too few for a reliable MT% filter, so none was applied
Doublet method
Scrublet (per library)
Integration method
Harmony on sample (4 libraries)
Cell-type annotation
Inherited from the source publication
Cell-type labels from
GSE289546_Opat.cell_to_cts.csv.gz (100% of cells matched)
Pipeline version
cnidosite-sc-1.0.0
Processed
2026-09-20T03:34:23+00:00
Clusters / cell types
55 / 31