Scrna qc
Execute the MAD-based single-cell RNA-seq QC workflow (scripts + Python API) to filter low-quality cells and emit reports plus filtered AnnData files.From its SKILL.md
npx -y skills add FridrichMethod/awesome-skills --skill scrna-qcAssembled from the repository path, not quoted from the project. Check it against their README if it does not work.
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SKILL.md
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At-a-Glance
- description (10-20 chars): QC autopilot
- keywords: scRNAseq, MAD, h5ad, QC, plots
Workflow
- Accept
.h5ad, 10x.h5, or 10x directory inputs; set mitochondrial/ribosomal patterns as needed. - Run
qc_analysis.py(CLI) or callqc_corehelpers to compute metrics, apply MAD thresholds, and filter cells/genes. - Generate standard plots (metrics before/after, threshold overlays) plus filtered data artifacts.
- Document parameters (mad_counts/genes/mt, mt_threshold, min_cells, log1p flag) inside the summary JSON.
- Provide guidance on next steps (doublet detection, downstream analysis).
Guardrails
- Adjust MT% expectations for tissue context; avoid over-filtering rare populations.
- This workflow is QC only—doublet handling and batch correction stay separate.
- Keep reproducibility by storing command invocations and environment info.
References
- See
README.md,qc_core.py,qc_analysis.py, andqc_plotting.pyfor API usage and schema details.
What ships with it: 5 files
36.2 KB alongside SKILL.md, 3 of them executable
- qc_analysis.pyruns12.1 KB
- qc_core.pyruns8.9 KB
- qc_plotting.pyruns9.5 KB
- README.md5.6 KB
- requirements.txt74 B