
Single-Cell RNA-seq QC
OfficialFreeAutomate quality control for single-cell RNA-seq data.
Free · Opens the source repo
What Single-Cell RNA-seq QC does
The Single-Cell RNA-seq Quality Control skill provides an automated workflow for performing quality control (QC) on single-cell RNA sequencing data, adhering to best practices established by scverse. This skill is particularly useful for researchers and bioinformaticians who need to ensure the integrity of their single-cell RNA-seq datasets before proceeding with downstream analyses. It supports input formats such as .h5ad and .h5, which are commonly used in single-cell genomics workflows.
The primary functionality is encapsulated in the qc_analysis.py script, which executes a complete QC pipeline that includes calculating QC metrics, applying MAD-based filtering, and generating comprehensive visualizations. Users can easily customize the filtering thresholds and other parameters through command-line options, making it flexible for various experimental conditions. For those who require more control over the QC process, the skill also offers modular functions in qc_core.py and qc_plotting.py, allowing users to build custom workflows tailored to their specific needs.
Outputs from the QC process include visualizations that compare pre- and post-filtering metrics, as well as filtered datasets ready for further analysis. This skill not only streamlines the QC process but also ensures that users can visualize and understand the impact of their filtering decisions. With detailed reference materials provided, users can gain insights into the rationale behind each QC metric and how to interpret the results effectively.
When to use it
Utilize this skill when conducting quality control on single-cell RNA-seq datasets, especially when following scverse best practices or needing to visualize QC metrics.
When not to use it
This skill may not be suitable for users looking for highly customized QC workflows that require extensive deviations from standard practices or those using non-supported file formats.
What you can build with it
Standard QC Workflow
Use the complete pipeline for standard QC on single-cell RNA-seq data to quickly filter low-quality cells.
Custom Analysis
Leverage modular functions for tailored QC processes that require specific filtering criteria or analysis steps.
Exploratory Data Analysis
Perform quick exploratory analysis on datasets to assess data quality and visualize QC metrics before deeper analysis.
How to install Single-Cell RNA-seq QC
View source1. Install with the skills CLI
npx skills add anthropics/knowledge-work-plugins/single-cell-rna-qc --agent claude-code2. Or install it manually
Download the skill folder and drop it into ~/.claude/skills/ for all projects, or .claude/skills/ to scope it to one repo. Restart Claude Code so it picks up the new skill.
Anthropic's agentic coding CLI, and the reference implementation of Agent Skills. Drop a skill folder into ~/.claude/skills and Claude Code loads it automatically whenever a task matches the skill's description. Claude Code docs
Inside SKILL.md
Written by anthropicsSingle-Cell RNA-seq Quality Control
Automated QC workflow for single-cell RNA-seq data following scverse best practices.
When to Use This Skill
Use when users:
- Request quality control or QC on single-cell RNA-seq data
- Want to filter low-quality cells or assess data quality
- Need QC visualizations or metrics
- Ask to follow scverse/scanpy best practices
- Request MAD-based filtering or outlier detection
Supported input formats:
.h5adfiles (AnnData format from scanpy/Python workflows).h5files (10X Genomics Cell Ranger output)
Default recommendation: Use Approach 1 (complete pipeline) unless the user has specific custom requirements or explicitly requests non-standard filtering logic.
Approach 1: Complete QC Pipeline (Recommended for Standard Workflows)
For standard QC following scverse best practices, use the convenience script scripts/qc_analysis.py:
python3 scripts/qc_analysis.py input.h5ad
# or for 10X Genomics .h5 files:
python3 scripts/qc_analysis.py raw_feature_bc_matrix.h5
The script automatically detects the file format and loads it appropriately.
When to use this approach:
- Standard QC workflow with adjustable thresholds (all cells filtered the same way)
- Batch processing multiple datasets
- Quick exploratory analysis
- User wants the "just works" solution
Requirements: anndata, scanpy, scipy, matplotlib, seaborn, numpy
Parameters:
Customize filtering thresholds and gene patterns using command-line parameters:
--output-dir- Output directory--mad-counts,--mad-genes,--mad-mt- MAD thresholds for counts/genes/MT%--mt-threshold- Hard mitochondrial % cutoff--min-cells- Gene filtering threshold--mt-pattern,--ribo-pattern,--hb-pattern- Gene name patterns for different species
Use --help to see current default values.
Outputs:
All files are saved to <input_basename>_qc_results/ directory by default (or to the directory specified by --output-dir):
qc_metrics_before_filtering.png- Pre-filtering visualizationsqc_filtering_thresholds.png- MAD-based threshold overlaysqc_metrics_after_filtering.png- Post-filtering quality metrics<input_basename>_filtered.h5ad- Clean, filtered dataset ready for downstream analysis<input_basename>_with_qc.h5ad- Original data with QC annotations preserved
If copying outputs for user access, copy individual files (not the entire directory) so users can preview them directly.
Workflow Steps
The script performs the following steps:
- Calculate QC metrics - Count depth, gene detection, mitochondrial/ribosomal/hemoglobin content
- Apply MAD-based filtering - Permissive outlier detection using MAD thresholds for counts/genes/MT%
- Filter genes - Remove genes detected in few cells
- Generate visualizations - Comprehensive before/after plots with threshold overlays
Approach 2: Modular Building Blocks (For Custom Workflows)
For custom analysis workflows or non-standard requirements, use the modular utility functions from scripts/qc_core.py and scripts/qc_plotting.py:
# Run from scripts/ directory, or add scripts/ to sys.path if needed
import anndata as ad
from qc_core import calculate_qc_metrics, detect_outliers_mad, filter_cells
from qc_plotting import plot_qc_distributions # Only if visualization needed
adata = ad.read_h5ad('input.h5ad')
calculate_qc_metrics(adata, inplace=True)
# ... custom analysis logic here
When to use this approach:
- Different workflow needed (skip steps, change order, apply different thresholds to subsets)
- Conditional logic (e.g., filter neurons differently than other cells)
- Partial execution (only metrics/visualization, no filtering)
- Integration with other analysis steps in a larger pipeline
- Custom filtering criteria beyond what command-line params support
Available utility functions:
From qc_core.py (core QC operations):
calculate_qc_metrics(adata, mt_pattern, ribo_pattern, hb_pattern, inplace=True)- Calculate QC metrics and annotate adatadetect_outliers_mad(adata, metric, n_mads, verbose=True)- MAD-based outlier detection, returns boolean maskapply_hard_threshold(adata, metric, threshold, operator='>', verbose=True)- Apply hard cutoffs, returns boolean maskfilter_cells(adata, mask, inplace=False)- Apply boolean mask to filter cellsfilter_genes(adata, min_cells=20, min_counts=None, inplace=True)- Filter genes by detectionprint_qc_summary(adata, label='')- Print summary statistics
From qc_plotting.py (visualization):
plot_qc_distributions(adata, output_path, title)- Generate comprehensive QC plotsplot_filtering_thresholds(adata, outlier_masks, thresholds, output_path)- Visualize filtering thresholdsplot_qc_after_filtering(adata, output_path)- Generate post-filtering plots
Example custom workflows:
Example 1: Only calculate metrics and visualize, don't filter yet
adata = ad.read_h5ad('input.h5ad')
calculate_qc_metrics(adata, inplace=True)
plot_qc_distributions(adata, 'qc_before.png', title='Initial QC')
print_qc_summary(adata, label='Before filtering')
Example 2: Apply only MT% filtering, keep other metrics permissive
adata = ad.read_h5ad('input.h5ad')
calculate_qc_metrics(adata, inplace=True)
# Only filter high MT% cells
high_mt = apply_hard_threshold(adata, 'pct_counts_mt', 10, operator='>')
adata_filtered = filter_cells(adata, ~high_mt)
adata_filtered.write('filtered.h5ad')
Example 3: Different thresholds for different subsets
adata = ad.read_h5ad('input.h5ad')
calculate_qc_metrics(adata, inplace=True)
# Apply type-specific QC (assumes cell_type metadata exists)
neurons = adata.obs['cell_type'] == 'neuron'
other_cells = ~neurons
# Neurons tolerate higher MT%, other cells use stricter threshold
neuron_qc = apply_hard_threshold(adata[neurons], 'pct_counts_mt', 15, operator='>')
other_qc = apply_hard_threshold(adata[other_cells], 'pct_counts_mt', 8, operator='>')
Best Practices
- Be permissive with filtering - Default thresholds intentionally retain most cells to avoid losing rare populations
- Inspect visualizations - Always review before/after plots to ensure filtering makes biological sense
- Consider dataset-specific factors - Some tissues naturally have higher mitochondrial content (e.g., neurons, cardiomyocytes)
- Check gene annotations - Mitochondrial gene prefixes vary by species (mt- for mouse, MT- for human)
- Iterate if needed - QC parameters may need adjustment based on the specific experiment or tissue type
Reference Materials
For detailed QC methodology, parameter rationale, and troubleshooting guidance, see references/scverse_qc_guidelines.md. This reference provides:
- Detailed explanations of each QC metric and why it matters
- Rationale for MAD-based thresholds and why they're better than fixed cutoffs
- Guidelines for interpreting QC visualizations (histograms, violin plots, scatter plots)
- Species-specific considerations for gene annotations
- When and how to adjust filtering parameters
- Advanced QC considerations (ambient RNA correction, doublet detection)
Load this reference when users need deeper understanding of the methodology or when troubleshooting QC issues.
Next Steps After QC
Typical downstream analysis steps:
- Ambient RNA correction (SoupX, CellBender)
- Doublet detection (scDblFinder)
- Normalization (log-normalize, scran)
- Feature selection and dimensionality reduction
- Clustering and cell type annotation
Frequently asked questions about Single-Cell RNA-seq QC
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