bio-spatial-transcriptomics-spatial-proteomics — independently scanned and version-tracked by SaferSkills.
SaferSkills independently audited bio-spatial-transcriptomics-spatial-proteomics (Agent Skill) and scored it 100/100 (green). The audit ran 55 deterministic rules across Security, Supply Chain, Maintenance, Transparency, and Community; it found 0 high-severity and 0 lower-severity findings. The full rule-by-rule trace and per-finding evidence are below. Free, methodology-open.
Findings & checks · 0 flagged
Every scanned point with the score it earned and what moved between them.
First recorded scan — no prior version to compare against.
The primary manifest — the file an agent reads to learn what this artifact does.
Reference examples tested with: anndata 0.10+, scanpy 1.10+, squidpy 1.3+
Before using code patterns, verify installed versions match. If versions differ:
pip show <package> then help(module.function) to check signaturesIf code throws ImportError, AttributeError, or TypeError, introspect the installed package and adapt the example to match the actual API rather than retrying.
"Analyze my CODEX/IMC spatial proteomics data" → Process multiplexed imaging data including cell segmentation, protein phenotyping, spatial neighborhood analysis, and protein colocalization scoring.
scimap.tl.phenotype_cells(), squidpy.gr.nhood_enrichment()Goal: Process multiplexed spatial proteomics data (CODEX/IMC/MIBI) through cell phenotyping, spatial neighborhood analysis, and protein colocalization scoring.
Approach: Load the cell-by-marker intensity matrix with spatial coordinates into AnnData, normalize and rescale marker intensities, phenotype cells by marker expression gating, then analyze spatial neighborhoods and cell-cell interactions using scimap and squidpy.
import scimap as sm
import anndata as ad
# Load CODEX/IMC data (cell x marker matrix with spatial coordinates)
adata = ad.read_h5ad('spatial_proteomics.h5ad')
# Required: spatial coordinates in adata.obsm['spatial']
# Required: protein intensities in adata.X# Log transform intensities
sm.pp.log1p(adata)
# Rescale markers (0-1 per marker)
sm.pp.rescale(adata)
# Combat batch correction if multiple FOVs
sm.pp.combat(adata, batch_key='fov')# Manual gating approach
phenotype_markers = {
'T_cell': ['CD3', 'CD45'],
'B_cell': ['CD20', 'CD45'],
'Macrophage': ['CD68', 'CD163'],
'Tumor': ['panCK', 'Ki67']
}
sm.tl.phenotype_cells(adata, phenotype=phenotype_markers,
gate=0.5, label='phenotype')
# Clustering-based phenotyping
sm.tl.cluster(adata, method='leiden', resolution=1.0)# Build spatial neighbors graph
sm.tl.spatial_distance(adata, x_coordinate='X', y_coordinate='Y')
# Neighborhood enrichment
sm.tl.spatial_interaction(adata, phenotype='phenotype',
method='knn', knn=10)
# Spatial clustering (communities of cells)
sm.tl.spatial_cluster(adata, phenotype='phenotype')# Spatial scatter plot
sm.pl.spatial_scatterPlot(adata, colorBy='phenotype',
x='X', y='Y', s=5)
# Heatmap of spatial interactions
sm.pl.spatial_interaction(adata)
# Marker expression overlay
sm.pl.image_viewer(adata, markers=['CD3', 'CD20', 'panCK'])import squidpy as sq
# If matched spatial transcriptomics available
# Transfer labels or integrate modalities
sq.gr.spatial_neighbors(adata_protein)
sq.gr.spatial_neighbors(adata_rna)
# Compare spatial patterns across modalities| Platform | Markers | Resolution | Notes |
|---|---|---|---|
| CODEX | 40-60 | Subcellular | Cyclic staining |
| IMC | 40+ | 1 um | Metal-tagged antibodies |
| MIBI | 40+ | 260 nm | Mass spectrometry |
~30 seconds. Free. No account. Every finding cites a rule and a line of evidence.