@mseep/open-computer-use 1.0.0

package/skills/examples/single-cell-rna-qc/scripts/qc_analysis.py

@@ -0,0 +1,232 @@
+#!/usr/bin/env python3
+"""
+Quality Control Analysis for Single-Cell RNA-seq Data
+Following scverse best practices from:
+https://www.sc-best-practices.org/preprocessing_visualization/quality_control.html
+
+This is a convenience script that runs a complete QC workflow using the
+modular functions from qc_core.py and qc_plotting.py.
+"""
+
+import anndata as ad
+import scanpy as sc
+import sys
+import os
+import argparse
+
+# Import our modular utilities
+from qc_core import (
+    calculate_qc_metrics,
+    detect_outliers_mad,
+    apply_hard_threshold,
+    filter_cells,
+    filter_genes,
+    print_qc_summary
+)
+from qc_plotting import (
+    plot_qc_distributions,
+    plot_filtering_thresholds,
+    plot_qc_after_filtering
+)
+
+print("=" * 80)
+print("Single-Cell RNA-seq Quality Control Analysis")
+print("=" * 80)
+
+# Default parameters (single source of truth)
+DEFAULT_MAD_COUNTS = 5
+DEFAULT_MAD_GENES = 5
+DEFAULT_MAD_MT = 3
+DEFAULT_MT_THRESHOLD = 8
+DEFAULT_MIN_CELLS = 20
+DEFAULT_MT_PATTERN = 'mt-,MT-'
+DEFAULT_RIBO_PATTERN = 'Rpl,Rps,RPL,RPS'
+DEFAULT_HB_PATTERN = '^Hb[^(p)]|^HB[^(P)]'
+
+# Parse command-line arguments
+parser = argparse.ArgumentParser(
+    description='Quality Control Analysis for Single-Cell RNA-seq Data',
+    formatter_class=argparse.RawDescriptionHelpFormatter,
+    epilog="""
+Examples:
+  python3 qc_analysis.py data.h5ad
+  python3 qc_analysis.py raw_feature_bc_matrix.h5
+  python3 qc_analysis.py data.h5ad --mad-counts 4 --mad-genes 4 --mad-mt 2.5
+  python3 qc_analysis.py data.h5ad --mt-threshold 10 --min-cells 10
+  python3 qc_analysis.py data.h5ad --mt-pattern "^mt-" --ribo-pattern "^Rpl,^Rps"
+    """
+)
+
+parser.add_argument('input_file', help='Input .h5ad or .h5 file (10X Genomics format)')
+parser.add_argument('--output-dir', type=str, help='Output directory (default: <input_basename>_qc_results)')
+parser.add_argument('--mad-counts', type=float, default=DEFAULT_MAD_COUNTS, help=f'MAD threshold for total counts (default: {DEFAULT_MAD_COUNTS})')
+parser.add_argument('--mad-genes', type=float, default=DEFAULT_MAD_GENES, help=f'MAD threshold for gene counts (default: {DEFAULT_MAD_GENES})')
+parser.add_argument('--mad-mt', type=float, default=DEFAULT_MAD_MT, help=f'MAD threshold for mitochondrial percentage (default: {DEFAULT_MAD_MT})')
+parser.add_argument('--mt-threshold', type=float, default=DEFAULT_MT_THRESHOLD, help=f'Hard threshold for mitochondrial percentage (default: {DEFAULT_MT_THRESHOLD})')
+parser.add_argument('--min-cells', type=int, default=DEFAULT_MIN_CELLS, help=f'Minimum cells for gene filtering (default: {DEFAULT_MIN_CELLS})')
+parser.add_argument('--mt-pattern', type=str, default=DEFAULT_MT_PATTERN, help=f'Comma-separated mitochondrial gene prefixes (default: "{DEFAULT_MT_PATTERN}")')
+parser.add_argument('--ribo-pattern', type=str, default=DEFAULT_RIBO_PATTERN, help=f'Comma-separated ribosomal gene prefixes (default: "{DEFAULT_RIBO_PATTERN}")')
+parser.add_argument('--hb-pattern', type=str, default=DEFAULT_HB_PATTERN, help=f'Hemoglobin gene regex pattern (default: "{DEFAULT_HB_PATTERN}")')
+
+args = parser.parse_args()
+
+# Verify input file exists
+if not os.path.exists(args.input_file):
+    print(f"\nError: File '{args.input_file}' not found!")
+    sys.exit(1)
+
+input_file = args.input_file
+base_name = os.path.splitext(os.path.basename(input_file))[0]
+
+# Set up output directory
+if args.output_dir:
+    output_dir = args.output_dir
+else:
+    output_dir = f"{base_name}_qc_results"
+
+os.makedirs(output_dir, exist_ok=True)
+print(f"\nOutput directory: {output_dir}")
+
+# Display parameters
+print(f"\nParameters:")
+print(f"  MAD thresholds: counts={args.mad_counts}, genes={args.mad_genes}, MT%={args.mad_mt}")
+print(f"  MT hard threshold: {args.mt_threshold}%")
+print(f"  Min cells for gene filtering: {args.min_cells}")
+print(f"  Gene patterns: MT={args.mt_pattern}, Ribo={args.ribo_pattern}")
+
+# Load the data
+print("\n[1/5] Loading data...")
+file_ext = os.path.splitext(input_file)[1].lower()
+
+if file_ext == '.h5ad':
+    adata = ad.read_h5ad(input_file)
+    print(f"Loaded .h5ad file: {adata.n_obs} cells × {adata.n_vars} genes")
+elif file_ext == '.h5':
+    adata = sc.read_10x_h5(input_file)
+    print(f"Loaded 10X .h5 file: {adata.n_obs} cells × {adata.n_vars} genes")
+    # Make variable names unique (10X data sometimes has duplicate gene names)
+    adata.var_names_make_unique()
+else:
+    print(f"\nError: Unsupported file format '{file_ext}'. Expected .h5ad or .h5")
+    sys.exit(1)
+
+# Store original counts for comparison
+n_cells_original = adata.n_obs
+n_genes_original = adata.n_vars
+
+# Calculate QC metrics
+print("\n[2/5] Calculating QC metrics...")
+calculate_qc_metrics(adata, mt_pattern=args.mt_pattern,
+                     ribo_pattern=args.ribo_pattern,
+                     hb_pattern=args.hb_pattern,
+                     inplace=True)
+
+print(f"  Found {adata.var['mt'].sum()} mitochondrial genes (pattern: {args.mt_pattern})")
+print(f"  Found {adata.var['ribo'].sum()} ribosomal genes (pattern: {args.ribo_pattern})")
+print(f"  Found {adata.var['hb'].sum()} hemoglobin genes (pattern: {args.hb_pattern})")
+
+print_qc_summary(adata, label='QC Metrics Summary (before filtering)')
+
+# Create before-filtering visualizations
+print("\n[3/5] Creating QC visualizations...")
+before_plot = os.path.join(output_dir, 'qc_metrics_before_filtering.png')
+plot_qc_distributions(adata, before_plot, title='Quality Control Metrics - Before Filtering')
+print(f"  Saved: {before_plot}")
+
+# Apply MAD-based filtering
+print("\n[4/5] Applying MAD-based filtering thresholds...")
+
+# Detect outliers for each metric
+adata.obs['outlier_counts'] = detect_outliers_mad(adata, 'total_counts', args.mad_counts)
+adata.obs['outlier_genes'] = detect_outliers_mad(adata, 'n_genes_by_counts', args.mad_genes)
+adata.obs['outlier_mt'] = detect_outliers_mad(adata, 'pct_counts_mt', args.mad_mt)
+
+# Apply hard threshold for mitochondrial content
+print(f"\n  Applying hard threshold for mitochondrial content (>{args.mt_threshold}%):")
+high_mt_mask = apply_hard_threshold(adata, 'pct_counts_mt', args.mt_threshold, operator='>')
+
+# Combine MT filters (MAD + hard threshold)
+adata.obs['outlier_mt'] = adata.obs['outlier_mt'] | high_mt_mask
+
+# Overall filtering decision
+adata.obs['pass_qc'] = ~(
+    adata.obs['outlier_counts'] |
+    adata.obs['outlier_genes'] |
+    adata.obs['outlier_mt']
+)
+
+print(f"\n  Total cells failing QC: {(~adata.obs['pass_qc']).sum()} ({(~adata.obs['pass_qc']).sum()/adata.n_obs*100:.2f}%)")
+print(f"  Cells passing QC: {adata.obs['pass_qc'].sum()} ({adata.obs['pass_qc'].sum()/adata.n_obs*100:.2f}%)")
+
+# Visualize filtering thresholds
+outlier_masks = {
+    'total_counts': adata.obs['outlier_counts'].values,
+    'n_genes_by_counts': adata.obs['outlier_genes'].values,
+    'pct_counts_mt': adata.obs['outlier_mt'].values
+}
+
+thresholds = {
+    'total_counts': {'n_mads': args.mad_counts},
+    'n_genes_by_counts': {'n_mads': args.mad_genes},
+    'pct_counts_mt': {'n_mads': args.mad_mt, 'hard': args.mt_threshold}
+}
+
+threshold_plot = os.path.join(output_dir, 'qc_filtering_thresholds.png')
+plot_filtering_thresholds(adata, outlier_masks, thresholds, threshold_plot)
+print(f"\n  Saved: {threshold_plot}")
+
+# Apply filtering
+print("\n[5/5] Applying filters...")
+adata_filtered = filter_cells(adata, adata.obs['pass_qc'].values, inplace=False)
+print(f"  Cells after filtering: {adata_filtered.n_obs} (removed {n_cells_original - adata_filtered.n_obs})")
+
+# Filter genes
+print(f"\n  Filtering genes detected in <{args.min_cells} cells...")
+filter_genes(adata_filtered, min_cells=args.min_cells, inplace=True)
+print(f"  Genes after filtering: {adata_filtered.n_vars} (removed {n_genes_original - adata_filtered.n_vars})")
+
+# Generate summary statistics
+print("\n" + "=" * 80)
+print("QC Summary")
+print("=" * 80)
+
+print("\nBefore filtering:")
+print(f"  Cells: {n_cells_original}")
+print(f"  Genes: {n_genes_original}")
+
+print("\nAfter filtering:")
+print(f"  Cells: {adata_filtered.n_obs} ({adata_filtered.n_obs/n_cells_original*100:.1f}% retained)")
+print(f"  Genes: {adata_filtered.n_vars} ({adata_filtered.n_vars/n_genes_original*100:.1f}% retained)")
+
+print_qc_summary(adata_filtered, label='\nFiltered data QC metrics')
+
+# Create after-filtering visualizations
+after_plot = os.path.join(output_dir, 'qc_metrics_after_filtering.png')
+plot_qc_after_filtering(adata_filtered, after_plot)
+print(f"\n  Saved: {after_plot}")
+
+# Save filtered data
+print("\nSaving filtered data...")
+output_filtered = os.path.join(output_dir, f'{base_name}_filtered.h5ad')
+output_with_qc = os.path.join(output_dir, f'{base_name}_with_qc.h5ad')
+adata_filtered.write(output_filtered)
+print(f"  Saved: {output_filtered}")
+
+# Also save the unfiltered data with QC annotations
+adata.write(output_with_qc)
+print(f"  Saved: {output_with_qc} (original data with QC annotations)")
+
+print("\n" + "=" * 80)
+print("Quality Control Analysis Complete!")
+print("=" * 80)
+print(f"\nAll results saved to: {output_dir}/")
+print("\nGenerated files:")
+print("  1. qc_metrics_before_filtering.png - Initial QC visualizations")
+print("  2. qc_filtering_thresholds.png - MAD-based threshold visualization")
+print("  3. qc_metrics_after_filtering.png - Post-filtering QC visualizations")
+print(f"  4. {base_name}_filtered.h5ad - Filtered dataset")
+print(f"  5. {base_name}_with_qc.h5ad - Original dataset with QC annotations")
+print("\nNext steps:")
+print("  - Consider ambient RNA correction (SoupX)")
+print("  - Consider doublet detection (scDblFinder)")
+print("  - Proceed with normalization and downstream analysis")

package/skills/examples/single-cell-rna-qc/scripts/qc_core.py

@@ -0,0 +1,233 @@
+#!/usr/bin/env python3
+"""
+Core utility functions for single-cell RNA-seq quality control.
+
+This module provides building blocks for metrics calculation and filtering
+while following scverse best practices from:
+https://www.sc-best-practices.org/preprocessing_visualization/quality_control.html
+"""
+
+import anndata as ad
+import scanpy as sc
+import numpy as np
+from scipy.stats import median_abs_deviation
+
+
+def calculate_qc_metrics(adata, mt_pattern='mt-,MT-', ribo_pattern='Rpl,Rps,RPL,RPS',
+                        hb_pattern='^Hb[^(p)]|^HB[^(P)]', inplace=True):
+    """
+    Calculate QC metrics for single-cell RNA-seq data.
+
+    Parameters
+    ----------
+    adata : AnnData
+        Annotated data matrix
+    mt_pattern : str
+        Comma-separated mitochondrial gene prefixes (default: 'mt-,MT-')
+    ribo_pattern : str
+        Comma-separated ribosomal gene prefixes (default: 'Rpl,Rps,RPL,RPS')
+    hb_pattern : str
+        Regex pattern for hemoglobin genes (default: '^Hb[^(p)]|^HB[^(P)]')
+    inplace : bool
+        Modify adata in place (default: True)
+
+    Returns
+    -------
+    AnnData or None
+        If inplace=False, returns modified AnnData. Otherwise modifies in place.
+    """
+    if not inplace:
+        adata = adata.copy()
+
+    # Identify gene categories
+    mt_prefixes = tuple(mt_pattern.split(','))
+    adata.var['mt'] = adata.var_names.str.startswith(mt_prefixes)
+
+    ribo_prefixes = tuple(ribo_pattern.split(','))
+    adata.var['ribo'] = adata.var_names.str.startswith(ribo_prefixes)
+
+    adata.var['hb'] = adata.var_names.str.match(hb_pattern)
+
+    # Calculate QC metrics
+    sc.pp.calculate_qc_metrics(
+        adata,
+        qc_vars=['mt', 'ribo', 'hb'],
+        percent_top=None,
+        log1p=False,
+        inplace=True
+    )
+
+    if not inplace:
+        return adata
+
+
+def detect_outliers_mad(adata, metric, n_mads, verbose=True):
+    """
+    Detect outliers using Median Absolute Deviation (MAD).
+
+    Parameters
+    ----------
+    adata : AnnData
+        Annotated data matrix with QC metrics
+    metric : str
+        Column name in adata.obs to use for outlier detection
+    n_mads : float
+        Number of MADs to use as threshold
+    verbose : bool
+        Print outlier statistics (default: True)
+
+    Returns
+    -------
+    np.ndarray
+        Boolean mask where True indicates outliers
+    """
+    metric_values = adata.obs[metric]
+    median = np.median(metric_values)
+    mad = median_abs_deviation(metric_values)
+
+    # Calculate bounds
+    lower = median - n_mads * mad
+    upper = median + n_mads * mad
+
+    # Identify outliers
+    outlier_mask = (metric_values < lower) | (metric_values > upper)
+
+    if verbose:
+        print(f"  {metric}:")
+        print(f"    Median: {median:.2f}, MAD: {mad:.2f}")
+        print(f"    Bounds: [{lower:.2f}, {upper:.2f}] ({n_mads} MADs)")
+        print(f"    Outliers: {outlier_mask.sum()} cells ({outlier_mask.sum()/len(metric_values)*100:.2f}%)")
+
+    return outlier_mask
+
+
+def apply_hard_threshold(adata, metric, threshold, operator='>', verbose=True):
+    """
+    Apply a hard threshold filter.
+
+    Parameters
+    ----------
+    adata : AnnData
+        Annotated data matrix
+    metric : str
+        Column name in adata.obs to filter on
+    threshold : float
+        Threshold value
+    operator : str
+        Comparison operator: '>', '<', '>=', '<=' (default: '>')
+    verbose : bool
+        Print filtering statistics (default: True)
+
+    Returns
+    -------
+    np.ndarray
+        Boolean mask where True indicates cells to filter out
+    """
+    metric_values = adata.obs[metric]
+
+    if operator == '>':
+        mask = metric_values > threshold
+    elif operator == '<':
+        mask = metric_values < threshold
+    elif operator == '>=':
+        mask = metric_values >= threshold
+    elif operator == '<=':
+        mask = metric_values <= threshold
+    else:
+        raise ValueError(f"Invalid operator: {operator}. Use '>', '<', '>=', or '<='")
+
+    if verbose:
+        print(f"  {metric} {operator} {threshold}:")
+        print(f"    Cells filtered: {mask.sum()} ({mask.sum()/len(metric_values)*100:.2f}%)")
+
+    return mask
+
+
+def filter_cells(adata, mask, inplace=False):
+    """
+    Filter cells based on a boolean mask.
+
+    Parameters
+    ----------
+    adata : AnnData
+        Annotated data matrix
+    mask : np.ndarray or pd.Series
+        Boolean mask where True indicates cells to KEEP
+    inplace : bool
+        Modify adata in place (default: False)
+
+    Returns
+    -------
+    AnnData
+        Filtered AnnData object
+    """
+    if inplace:
+        # This is actually a bit tricky - AnnData doesn't support true inplace filtering
+        # Return filtered copy which caller should reassign
+        return adata[mask].copy()
+    else:
+        return adata[mask].copy()
+
+
+def filter_genes(adata, min_cells=20, min_counts=None, inplace=True):
+    """
+    Filter genes based on detection thresholds.
+
+    Parameters
+    ----------
+    adata : AnnData
+        Annotated data matrix
+    min_cells : int
+        Minimum number of cells a gene must be detected in (default: 20)
+    min_counts : int, optional
+        Minimum total counts across all cells
+    inplace : bool
+        Modify adata in place (default: True)
+
+    Returns
+    -------
+    AnnData or None
+        If inplace=False, returns filtered AnnData
+    """
+    if not inplace:
+        adata = adata.copy()
+
+    if min_cells is not None:
+        sc.pp.filter_genes(adata, min_cells=min_cells)
+
+    if min_counts is not None:
+        sc.pp.filter_genes(adata, min_counts=min_counts)
+
+    if not inplace:
+        return adata
+
+
+def print_qc_summary(adata, label=''):
+    """
+    Print summary statistics for QC metrics.
+
+    Parameters
+    ----------
+    adata : AnnData
+        Annotated data matrix with QC metrics
+    label : str
+        Label to prepend to output (e.g., 'Before filtering', 'After filtering')
+    """
+    if label:
+        print(f"\n{label}:")
+    print(f"  Cells: {adata.n_obs}")
+    print(f"  Genes: {adata.n_vars}")
+
+    if 'total_counts' in adata.obs:
+        print(f"  Mean counts per cell: {adata.obs['total_counts'].mean():.0f}")
+        print(f"  Median counts per cell: {adata.obs['total_counts'].median():.0f}")
+
+    if 'n_genes_by_counts' in adata.obs:
+        print(f"  Mean genes per cell: {adata.obs['n_genes_by_counts'].mean():.0f}")
+        print(f"  Median genes per cell: {adata.obs['n_genes_by_counts'].median():.0f}")
+
+    if 'pct_counts_mt' in adata.obs:
+        print(f"  Mean mitochondrial %: {adata.obs['pct_counts_mt'].mean():.2f}%")
+
+    if 'pct_counts_ribo' in adata.obs:
+        print(f"  Mean ribosomal %: {adata.obs['pct_counts_ribo'].mean():.2f}%")

package/skills/examples/single-cell-rna-qc/scripts/qc_plotting.py

@@ -0,0 +1,235 @@
+#!/usr/bin/env python3
+"""
+Visualization functions for single-cell RNA-seq quality control.
+
+This module provides plotting utilities for QC metrics and filtering thresholds.
+"""
+
+import numpy as np
+import matplotlib.pyplot as plt
+from scipy.stats import median_abs_deviation
+
+
+def plot_qc_distributions(adata, output_path, title='Quality Control Metrics'):
+    """
+    Create comprehensive QC distribution plots.
+
+    Parameters
+    ----------
+    adata : AnnData
+        Annotated data matrix with QC metrics
+    output_path : str
+        Path to save the figure
+    title : str
+        Figure title (default: 'Quality Control Metrics')
+    """
+    fig, axes = plt.subplots(3, 3, figsize=(15, 12))
+    fig.suptitle(title, fontsize=16, y=0.995)
+
+    # Row 1: Histograms
+    axes[0, 0].hist(adata.obs['total_counts'], bins=100, color='steelblue', edgecolor='black')
+    axes[0, 0].set_xlabel('Total counts per cell')
+    axes[0, 0].set_ylabel('Number of cells')
+    axes[0, 0].set_title('Distribution of Total Counts')
+    axes[0, 0].axvline(adata.obs['total_counts'].median(), color='red', linestyle='--', label='Median')
+    axes[0, 0].legend()
+
+    axes[0, 1].hist(adata.obs['n_genes_by_counts'], bins=100, color='forestgreen', edgecolor='black')
+    axes[0, 1].set_xlabel('Genes per cell')
+    axes[0, 1].set_ylabel('Number of cells')
+    axes[0, 1].set_title('Distribution of Detected Genes')
+    axes[0, 1].axvline(adata.obs['n_genes_by_counts'].median(), color='red', linestyle='--', label='Median')
+    axes[0, 1].legend()
+
+    axes[0, 2].hist(adata.obs['pct_counts_mt'], bins=100, color='coral', edgecolor='black')
+    axes[0, 2].set_xlabel('Mitochondrial %')
+    axes[0, 2].set_ylabel('Number of cells')
+    axes[0, 2].set_title('Distribution of Mitochondrial Content')
+    axes[0, 2].axvline(adata.obs['pct_counts_mt'].median(), color='red', linestyle='--', label='Median')
+    axes[0, 2].legend()
+
+    # Row 2: Violin plots
+    axes[1, 0].violinplot([adata.obs['total_counts']], positions=[0], showmeans=True, showmedians=True)
+    axes[1, 0].set_ylabel('Total counts')
+    axes[1, 0].set_title('Total Counts per Cell')
+    axes[1, 0].set_xticks([])
+
+    axes[1, 1].violinplot([adata.obs['n_genes_by_counts']], positions=[0], showmeans=True, showmedians=True)
+    axes[1, 1].set_ylabel('Genes detected')
+    axes[1, 1].set_title('Genes per Cell')
+    axes[1, 1].set_xticks([])
+
+    axes[1, 2].violinplot([adata.obs['pct_counts_mt']], positions=[0], showmeans=True, showmedians=True)
+    axes[1, 2].set_ylabel('Mitochondrial %')
+    axes[1, 2].set_title('Mitochondrial Content')
+    axes[1, 2].set_xticks([])
+
+    # Row 3: Scatter plots
+    scatter1 = axes[2, 0].scatter(
+        adata.obs['total_counts'],
+        adata.obs['n_genes_by_counts'],
+        c=adata.obs['pct_counts_mt'],
+        cmap='viridis',
+        alpha=0.5,
+        s=10
+    )
+    axes[2, 0].set_xlabel('Total counts')
+    axes[2, 0].set_ylabel('Genes detected')
+    axes[2, 0].set_title('Counts vs Genes (colored by MT%)')
+    plt.colorbar(scatter1, ax=axes[2, 0], label='MT %')
+
+    axes[2, 1].scatter(
+        adata.obs['total_counts'],
+        adata.obs['pct_counts_mt'],
+        alpha=0.5,
+        s=10,
+        color='coral'
+    )
+    axes[2, 1].set_xlabel('Total counts')
+    axes[2, 1].set_ylabel('Mitochondrial %')
+    axes[2, 1].set_title('Total Counts vs Mitochondrial %')
+
+    axes[2, 2].scatter(
+        adata.obs['n_genes_by_counts'],
+        adata.obs['pct_counts_mt'],
+        alpha=0.5,
+        s=10,
+        color='forestgreen'
+    )
+    axes[2, 2].set_xlabel('Genes detected')
+    axes[2, 2].set_ylabel('Mitochondrial %')
+    axes[2, 2].set_title('Genes vs Mitochondrial %')
+
+    plt.tight_layout()
+    plt.savefig(output_path, dpi=300, bbox_inches='tight')
+    plt.close()
+
+
+def plot_filtering_thresholds(adata, outlier_masks, thresholds, output_path):
+    """
+    Visualize filtering thresholds overlaid on distributions.
+
+    Parameters
+    ----------
+    adata : AnnData
+        Annotated data matrix with QC metrics
+    outlier_masks : dict
+        Dictionary mapping metric names to boolean outlier masks
+        Example: {'total_counts': mask1, 'n_genes_by_counts': mask2, 'pct_counts_mt': mask3}
+    thresholds : dict
+        Dictionary with threshold information for each metric
+        Example: {'total_counts': {'n_mads': 5}, 'pct_counts_mt': {'n_mads': 3, 'hard': 8}}
+    output_path : str
+        Path to save the figure
+    """
+    fig, axes = plt.subplots(1, 3, figsize=(15, 4))
+    fig.suptitle('MAD-Based Filtering Thresholds', fontsize=16)
+
+    # Helper function to plot with thresholds
+    def plot_with_threshold(ax, metric, outlier_mask, n_mads, hard_threshold=None):
+        data = adata.obs[metric]
+        median = np.median(data)
+        mad = median_abs_deviation(data)
+        lower = median - n_mads * mad
+        upper = median + n_mads * mad
+
+        ax.hist(data[~outlier_mask], bins=100, alpha=0.7, label='Pass QC', color='steelblue')
+        ax.hist(data[outlier_mask], bins=100, alpha=0.7, label='Fail QC', color='coral')
+        ax.axvline(lower, color='red', linestyle='--', linewidth=2, label=f'Thresholds ({n_mads} MADs)')
+        ax.axvline(upper, color='red', linestyle='--', linewidth=2)
+
+        if hard_threshold is not None:
+            ax.axvline(hard_threshold, color='darkred', linestyle=':', linewidth=2,
+                      label=f'Hard threshold ({hard_threshold})')
+
+        ax.set_xlabel(metric.replace('_', ' ').title())
+        ax.set_ylabel('Number of cells')
+        ax.legend()
+
+    # Plot each metric
+    metrics = [
+        ('total_counts', 'Total Counts'),
+        ('n_genes_by_counts', 'Genes Detected'),
+        ('pct_counts_mt', 'Mitochondrial %')
+    ]
+
+    for idx, (metric, label) in enumerate(metrics):
+        if metric in outlier_masks and metric in thresholds:
+            hard = thresholds[metric].get('hard', None)
+            plot_with_threshold(axes[idx], metric, outlier_masks[metric],
+                              thresholds[metric]['n_mads'], hard)
+
+    plt.tight_layout()
+    plt.savefig(output_path, dpi=300, bbox_inches='tight')
+    plt.close()
+
+
+def plot_qc_after_filtering(adata, output_path):
+    """
+    Create QC plots for filtered data (simplified version without outlier overlay).
+
+    Parameters
+    ----------
+    adata : AnnData
+        Filtered annotated data matrix with QC metrics
+    output_path : str
+        Path to save the figure
+    """
+    fig, axes = plt.subplots(2, 3, figsize=(15, 8))
+    fig.suptitle('Quality Control Metrics - After Filtering', fontsize=16, y=0.995)
+
+    # Row 1: Histograms
+    axes[0, 0].hist(adata.obs['total_counts'], bins=100, color='steelblue', edgecolor='black')
+    axes[0, 0].set_xlabel('Total counts per cell')
+    axes[0, 0].set_ylabel('Number of cells')
+    axes[0, 0].set_title('Distribution of Total Counts')
+
+    axes[0, 1].hist(adata.obs['n_genes_by_counts'], bins=100, color='forestgreen', edgecolor='black')
+    axes[0, 1].set_xlabel('Genes per cell')
+    axes[0, 1].set_ylabel('Number of cells')
+    axes[0, 1].set_title('Distribution of Detected Genes')
+
+    axes[0, 2].hist(adata.obs['pct_counts_mt'], bins=100, color='coral', edgecolor='black')
+    axes[0, 2].set_xlabel('Mitochondrial %')
+    axes[0, 2].set_ylabel('Number of cells')
+    axes[0, 2].set_title('Distribution of Mitochondrial Content')
+
+    # Row 2: Scatter plots
+    scatter1 = axes[1, 0].scatter(
+        adata.obs['total_counts'],
+        adata.obs['n_genes_by_counts'],
+        c=adata.obs['pct_counts_mt'],
+        cmap='viridis',
+        alpha=0.5,
+        s=10
+    )
+    axes[1, 0].set_xlabel('Total counts')
+    axes[1, 0].set_ylabel('Genes detected')
+    axes[1, 0].set_title('Counts vs Genes (colored by MT%)')
+    plt.colorbar(scatter1, ax=axes[1, 0], label='MT %')
+
+    axes[1, 1].scatter(
+        adata.obs['total_counts'],
+        adata.obs['pct_counts_mt'],
+        alpha=0.5,
+        s=10,
+        color='coral'
+    )
+    axes[1, 1].set_xlabel('Total counts')
+    axes[1, 1].set_ylabel('Mitochondrial %')
+    axes[1, 1].set_title('Total Counts vs Mitochondrial %')
+
+    axes[1, 2].scatter(
+        adata.obs['n_genes_by_counts'],
+        adata.obs['pct_counts_mt'],
+        alpha=0.5,
+        s=10,
+        color='forestgreen'
+    )
+    axes[1, 2].set_xlabel('Genes detected')
+    axes[1, 2].set_ylabel('Mitochondrial %')
+    axes[1, 2].set_title('Genes vs Mitochondrial %')
+
+    plt.tight_layout()
+    plt.savefig(output_path, dpi=300, bbox_inches='tight')
+    plt.close()