@synsci/cli-darwin-x64 1.1.97 → 1.1.99

package/bin/skills/pathml/references/multiparametric.md

@@ -1,686 +0,0 @@
-# Multiparametric Imaging
-
-## Overview
-
-PathML provides specialized support for multiparametric imaging technologies that simultaneously measure multiple markers at single-cell resolution. These techniques include CODEX, Vectra multiplex immunofluorescence, MERFISH, and other spatial proteomics and transcriptomics platforms. PathML handles the unique data structures, processing requirements, and quantification workflows specific to each technology.
-
-## Supported Technologies
-
-### CODEX (CO-Detection by indEXing)
-- Cyclic immunofluorescence imaging
-- 40+ protein markers simultaneously
-- Single-cell spatial proteomics
-- Multi-cycle acquisition with antibody barcoding
-
-### Vectra Polaris
-- Multispectral multiplex immunofluorescence
-- 6-8 markers per slide
-- Spectral unmixing
-- Whole-slide scanning
-
-### MERFISH (Multiplexed Error-Robust FISH)
-- Spatial transcriptomics
-- 100s-1000s of genes
-- Single-molecule resolution
-- Error-correcting barcodes
-
-### Other Platforms
-- CycIF (Cyclic Immunofluorescence)
-- IMC (Imaging Mass Cytometry)
-- MIBI (Multiplexed Ion Beam Imaging)
-
-## CODEX Workflows
-
-### Loading CODEX Data
-
-CODEX data is typically organized in multi-channel image stacks from multiple acquisition cycles:
-
-```python
-from pathml.core import CODEXSlide
-
-# Load CODEX dataset
-codex_slide = CODEXSlide(
-    path='path/to/codex_directory',
-    stain='IF',  # Immunofluorescence
-    backend='bioformats'
-)
-
-# Inspect channels and cycles
-print(f"Number of channels: {codex_slide.num_channels}")
-print(f"Channel names: {codex_slide.channel_names}")
-print(f"Number of cycles: {codex_slide.num_cycles}")
-print(f"Image shape: {codex_slide.shape}")
-```
-
-**CODEX directory structure:**
-```
-codex_directory/
-├── cyc001_reg001/
-│   ├── 1_00001_Z001_CH1.tif
-│   ├── 1_00001_Z001_CH2.tif
-│   └── ...
-├── cyc002_reg001/
-│   └── ...
-└── channelnames.txt
-```
-
-### CODEX Preprocessing Pipeline
-
-Complete pipeline for CODEX data processing:
-
-```python
-from pathml.preprocessing import Pipeline, CollapseRunsCODEX, SegmentMIF, QuantifyMIF
-
-# Create CODEX-specific pipeline
-codex_pipeline = Pipeline([
-    # 1. Collapse multi-cycle data
-    CollapseRunsCODEX(
-        z_slice=2,  # Select focal plane from z-stack
-        run_order=None,  # Automatic cycle ordering, or specify [0, 1, 2, ...]
-        method='max'  # 'max', 'mean', or 'median' across cycles
-    ),
-
-    # 2. Cell segmentation using Mesmer
-    SegmentMIF(
-        nuclear_channel='DAPI',
-        cytoplasm_channel='CD45',  # Or other membrane/cytoplasm marker
-        model='mesmer',
-        image_resolution=0.377,  # Microns per pixel
-        compartment='whole-cell'  # 'nuclear', 'cytoplasm', or 'whole-cell'
-    ),
-
-    # 3. Quantify marker expression per cell
-    QuantifyMIF(
-        segmentation_mask_name='cell_segmentation',
-        markers=[
-            'DAPI', 'CD3', 'CD4', 'CD8', 'CD20', 'CD45',
-            'CD68', 'PD1', 'PDL1', 'Ki67', 'panCK'
-        ],
-        output_format='anndata'
-    )
-])
-
-# Run pipeline
-codex_pipeline.run(codex_slide)
-
-# Access results
-segmentation_mask = codex_slide.masks['cell_segmentation']
-cell_data = codex_slide.cell_data  # AnnData object
-```
-
-### CollapseRunsCODEX
-
-Consolidates multi-cycle CODEX acquisitions into a single multi-channel image:
-
-```python
-from pathml.preprocessing import CollapseRunsCODEX
-
-transform = CollapseRunsCODEX(
-    z_slice=2,  # Select which z-plane (0-indexed)
-    run_order=[0, 1, 2, 3],  # Order of acquisition cycles
-    method='max',  # Aggregation method across cycles
-    background_subtract=True,  # Subtract background fluorescence
-    channel_mapping=None  # Optional: remap channel order
-)
-```
-
-**Parameters:**
-- `z_slice`: Which focal plane to extract from z-stacks (typically middle slice)
-- `run_order`: Order of cycles; None for automatic detection
-- `method`: How to combine channels from multiple cycles ('max', 'mean', 'median')
-- `background_subtract`: Whether to subtract background fluorescence
-
-**Output:** Single multi-channel image with all markers (H, W, C)
-
-### Cell Segmentation with Mesmer
-
-DeepCell Mesmer provides accurate cell segmentation for multiparametric imaging:
-
-```python
-from pathml.preprocessing import SegmentMIF
-
-transform = SegmentMIF(
-    nuclear_channel='DAPI',  # Nuclear marker (required)
-    cytoplasm_channel='CD45',  # Cytoplasm/membrane marker (required)
-    model='mesmer',  # DeepCell Mesmer model
-    image_resolution=0.377,  # Microns per pixel (important for accuracy)
-    compartment='whole-cell',  # Segmentation output
-    min_cell_size=50,  # Minimum cell size in pixels
-    max_cell_size=1000  # Maximum cell size in pixels
-)
-```
-
-**Choosing cytoplasm channel:**
-- **CD45**: Pan-leukocyte marker (good for immune-rich tissues)
-- **panCK**: Pan-cytokeratin (good for epithelial tissues)
-- **CD298/b2m**: Universal membrane marker
-- **Combination**: Average multiple membrane markers
-
-**Compartment options:**
-- `'whole-cell'`: Full cell segmentation (nucleus + cytoplasm)
-- `'nuclear'`: Nuclear segmentation only
-- `'cytoplasm'`: Cytoplasmic compartment only
-
-### Remote Segmentation
-
-Use DeepCell cloud API for segmentation without local GPU:
-
-```python
-from pathml.preprocessing import SegmentMIFRemote
-
-transform = SegmentMIFRemote(
-    nuclear_channel='DAPI',
-    cytoplasm_channel='CD45',
-    model='mesmer',
-    api_url='https://deepcell.org/api/predict',
-    timeout=300  # Timeout in seconds
-)
-```
-
-### Marker Quantification
-
-Extract single-cell marker expression from segmented images:
-
-```python
-from pathml.preprocessing import QuantifyMIF
-
-transform = QuantifyMIF(
-    segmentation_mask_name='cell_segmentation',
-    markers=['DAPI', 'CD3', 'CD4', 'CD8', 'CD20', 'CD68', 'panCK'],
-    output_format='anndata',  # or 'dataframe'
-    statistics=['mean', 'median', 'std', 'total'],  # Aggregation methods
-    compartments=['whole-cell', 'nuclear', 'cytoplasm']  # If multiple masks
-)
-```
-
-**Output:** AnnData object with:
-- `adata.X`: Marker expression matrix (cells × markers)
-- `adata.obs`: Cell metadata (cell ID, coordinates, area, etc.)
-- `adata.var`: Marker metadata
-- `adata.obsm['spatial']`: Cell centroid coordinates
-
-### Integration with AnnData
-
-Process multiple CODEX slides into unified AnnData object:
-
-```python
-from pathml.core import SlideDataset
-import anndata as ad
-
-# Process multiple slides
-slide_paths = ['slide1', 'slide2', 'slide3']
-dataset = SlideDataset(
-    [CODEXSlide(p, stain='IF') for p in slide_paths]
-)
-
-# Run pipeline on all slides
-dataset.run(codex_pipeline, distributed=True, n_workers=8)
-
-# Combine into single AnnData
-adatas = []
-for slide in dataset:
-    adata = slide.cell_data
-    adata.obs['slide_id'] = slide.name
-    adatas.append(adata)
-
-# Concatenate
-combined_adata = ad.concat(adatas, join='outer', label='batch', keys=slide_paths)
-
-# Save for downstream analysis
-combined_adata.write('codex_dataset.h5ad')
-```
-
-## Vectra Workflows
-
-### Loading Vectra Data
-
-Vectra stores data in proprietary `.qptiff` format:
-
-```python
-from pathml.core import SlideData, SlideType
-
-# Load Vectra slide
-vectra_slide = SlideData.from_slide(
-    'path/to/slide.qptiff',
-    backend=SlideType.VectraQPTIFF
-)
-
-# Access spectral channels
-print(f"Channels: {vectra_slide.channel_names}")
-```
-
-### Vectra Preprocessing
-
-```python
-from pathml.preprocessing import Pipeline, CollapseRunsVectra, SegmentMIF, QuantifyMIF
-
-vectra_pipeline = Pipeline([
-    # 1. Process Vectra multi-channel data
-    CollapseRunsVectra(
-        wavelengths=[520, 540, 570, 620, 670, 780],  # Emission wavelengths
-        unmix=True,  # Apply spectral unmixing
-        autofluorescence_correction=True
-    ),
-
-    # 2. Cell segmentation
-    SegmentMIF(
-        nuclear_channel='DAPI',
-        cytoplasm_channel='FITC',
-        model='mesmer',
-        image_resolution=0.5
-    ),
-
-    # 3. Quantification
-    QuantifyMIF(
-        segmentation_mask_name='cell_segmentation',
-        markers=['DAPI', 'CD3', 'CD8', 'PD1', 'PDL1', 'panCK'],
-        output_format='anndata'
-    )
-])
-
-vectra_pipeline.run(vectra_slide)
-```
-
-## Downstream Analysis
-
-### Cell Type Annotation
-
-Annotate cells based on marker expression:
-
-```python
-import anndata as ad
-import numpy as np
-
-# Load quantified data
-adata = ad.read_h5ad('codex_dataset.h5ad')
-
-# Define cell types by marker thresholds
-def annotate_cell_types(adata, thresholds):
-    cell_types = np.full(adata.n_obs, 'Unknown', dtype=object)
-
-    # T cells: CD3+
-    cd3_pos = adata[:, 'CD3'].X.flatten() > thresholds['CD3']
-    cell_types[cd3_pos] = 'T cell'
-
-    # CD4 T cells: CD3+ CD4+ CD8-
-    cd4_tcells = (
-        (adata[:, 'CD3'].X.flatten() > thresholds['CD3']) &
-        (adata[:, 'CD4'].X.flatten() > thresholds['CD4']) &
-        (adata[:, 'CD8'].X.flatten() < thresholds['CD8'])
-    )
-    cell_types[cd4_tcells] = 'CD4 T cell'
-
-    # CD8 T cells: CD3+ CD8+ CD4-
-    cd8_tcells = (
-        (adata[:, 'CD3'].X.flatten() > thresholds['CD3']) &
-        (adata[:, 'CD8'].X.flatten() > thresholds['CD8']) &
-        (adata[:, 'CD4'].X.flatten() < thresholds['CD4'])
-    )
-    cell_types[cd8_tcells] = 'CD8 T cell'
-
-    # B cells: CD20+
-    b_cells = adata[:, 'CD20'].X.flatten() > thresholds['CD20']
-    cell_types[b_cells] = 'B cell'
-
-    # Macrophages: CD68+
-    macrophages = adata[:, 'CD68'].X.flatten() > thresholds['CD68']
-    cell_types[macrophages] = 'Macrophage'
-
-    # Tumor cells: panCK+
-    tumor = adata[:, 'panCK'].X.flatten() > thresholds['panCK']
-    cell_types[tumor] = 'Tumor'
-
-    return cell_types
-
-# Apply annotation
-thresholds = {
-    'CD3': 0.5,
-    'CD4': 0.4,
-    'CD8': 0.4,
-    'CD20': 0.3,
-    'CD68': 0.3,
-    'panCK': 0.5
-}
-
-adata.obs['cell_type'] = annotate_cell_types(adata, thresholds)
-
-# Visualize cell type composition
-import matplotlib.pyplot as plt
-cell_type_counts = adata.obs['cell_type'].value_counts()
-plt.figure(figsize=(10, 6))
-cell_type_counts.plot(kind='bar')
-plt.xlabel('Cell Type')
-plt.ylabel('Count')
-plt.title('Cell Type Composition')
-plt.xticks(rotation=45)
-plt.tight_layout()
-plt.show()
-```
-
-### Clustering
-
-Unsupervised clustering to identify cell populations:
-
-```python
-import scanpy as sc
-
-# Preprocessing for clustering
-sc.pp.normalize_total(adata, target_sum=1e4)
-sc.pp.log1p(adata)
-sc.pp.scale(adata, max_value=10)
-
-# PCA
-sc.tl.pca(adata, n_comps=50)
-
-# Neighborhood graph
-sc.pp.neighbors(adata, n_neighbors=15, n_pcs=30)
-
-# UMAP embedding
-sc.tl.umap(adata)
-
-# Leiden clustering
-sc.tl.leiden(adata, resolution=0.5)
-
-# Visualize
-sc.pl.umap(adata, color=['leiden', 'CD3', 'CD8', 'CD20', 'panCK'])
-```
-
-### Spatial Visualization
-
-Visualize cells in spatial context:
-
-```python
-import matplotlib.pyplot as plt
-
-# Spatial scatter plot
-fig, ax = plt.subplots(figsize=(15, 15))
-
-# Color by cell type
-cell_types = adata.obs['cell_type'].unique()
-colors = plt.cm.tab10(np.linspace(0, 1, len(cell_types)))
-
-for i, cell_type in enumerate(cell_types):
-    mask = adata.obs['cell_type'] == cell_type
-    coords = adata.obsm['spatial'][mask]
-    ax.scatter(
-        coords[:, 0],
-        coords[:, 1],
-        c=[colors[i]],
-        label=cell_type,
-        s=5,
-        alpha=0.7
-    )
-
-ax.legend(markerscale=2)
-ax.set_xlabel('X (pixels)')
-ax.set_ylabel('Y (pixels)')
-ax.set_title('Spatial Cell Type Distribution')
-ax.axis('equal')
-plt.tight_layout()
-plt.show()
-```
-
-### Spatial Neighborhood Analysis
-
-Analyze cell neighborhoods and interactions:
-
-```python
-import squidpy as sq
-
-# Calculate spatial neighborhood enrichment
-sq.gr.spatial_neighbors(adata, coord_type='generic', spatial_key='spatial')
-
-# Neighborhood enrichment test
-sq.gr.nhood_enrichment(adata, cluster_key='cell_type')
-
-# Visualize interaction matrix
-sq.pl.nhood_enrichment(adata, cluster_key='cell_type')
-
-# Co-occurrence score
-sq.gr.co_occurrence(adata, cluster_key='cell_type')
-sq.pl.co_occurrence(
-    adata,
-    cluster_key='cell_type',
-    clusters=['CD8 T cell', 'Tumor'],
-    figsize=(8, 8)
-)
-```
-
-### Spatial Autocorrelation
-
-Test for spatial clustering of markers:
-
-```python
-# Moran's I spatial autocorrelation
-sq.gr.spatial_autocorr(
-    adata,
-    mode='moran',
-    genes=['CD3', 'CD8', 'PD1', 'PDL1', 'panCK']
-)
-
-# Visualize
-results = adata.uns['moranI']
-print(results.head())
-```
-
-## MERFISH Workflows
-
-### Loading MERFISH Data
-
-```python
-from pathml.core import MERFISHSlide
-
-# Load MERFISH dataset
-merfish_slide = MERFISHSlide(
-    path='path/to/merfish_data',
-    fov_size=2048,  # Field of view size
-    microns_per_pixel=0.108
-)
-```
-
-### MERFISH Processing
-
-```python
-from pathml.preprocessing import Pipeline, DecodeMERFISH, SegmentMIF
-
-merfish_pipeline = Pipeline([
-    # 1. Decode barcodes to genes
-    DecodeMERFISH(
-        codebook='path/to/codebook.csv',
-        error_correction=True,
-        distance_threshold=0.5
-    ),
-
-    # 2. Cell segmentation
-    SegmentMIF(
-        nuclear_channel='DAPI',
-        cytoplasm_channel='polyT',  # poly(T) stain for cell boundaries
-        model='mesmer'
-    ),
-
-    # 3. Assign transcripts to cells
-    AssignTranscripts(
-        segmentation_mask_name='cell_segmentation',
-        transcript_coords='decoded_spots'
-    )
-])
-
-merfish_pipeline.run(merfish_slide)
-
-# Output: AnnData with gene counts per cell
-gene_expression = merfish_slide.cell_data
-```
-
-## Quality Control
-
-### Segmentation Quality
-
-```python
-from pathml.utils import assess_segmentation_quality
-
-# Check segmentation quality metrics
-qc_metrics = assess_segmentation_quality(
-    segmentation_mask,
-    image,
-    metrics=['cell_count', 'mean_cell_size', 'size_distribution']
-)
-
-print(f"Total cells: {qc_metrics['cell_count']}")
-print(f"Mean cell size: {qc_metrics['mean_cell_size']:.1f} pixels")
-
-# Visualize
-import matplotlib.pyplot as plt
-plt.hist(qc_metrics['cell_sizes'], bins=50)
-plt.xlabel('Cell Size (pixels)')
-plt.ylabel('Frequency')
-plt.title('Cell Size Distribution')
-plt.show()
-```
-
-### Marker Expression QC
-
-```python
-import scanpy as sc
-
-# Load AnnData
-adata = ad.read_h5ad('codex_dataset.h5ad')
-
-# Calculate QC metrics
-adata.obs['total_intensity'] = adata.X.sum(axis=1)
-adata.obs['n_markers_detected'] = (adata.X > 0).sum(axis=1)
-
-# Filter low-quality cells
-adata = adata[adata.obs['total_intensity'] > 100, :]
-adata = adata[adata.obs['n_markers_detected'] >= 3, :]
-
-# Visualize
-sc.pl.violin(adata, ['total_intensity', 'n_markers_detected'], multi_panel=True)
-```
-
-## Batch Processing
-
-Process large multiparametric datasets efficiently:
-
-```python
-from pathml.core import SlideDataset
-from pathml.preprocessing import Pipeline
-from dask.distributed import Client
-import glob
-
-# Start Dask cluster
-client = Client(n_workers=16, threads_per_worker=2, memory_limit='8GB')
-
-# Find all CODEX slides
-slide_dirs = glob.glob('data/codex_slides/*/')
-
-# Create dataset
-codex_slides = [CODEXSlide(d, stain='IF') for d in slide_dirs]
-dataset = SlideDataset(codex_slides)
-
-# Run pipeline in parallel
-dataset.run(
-    codex_pipeline,
-    distributed=True,
-    client=client,
-    scheduler='distributed'
-)
-
-# Save processed data
-for i, slide in enumerate(dataset):
-    slide.cell_data.write(f'processed/slide_{i}.h5ad')
-
-client.close()
-```
-
-## Integration with Other Tools
-
-### Export to Spatial Analysis Tools
-
-```python
-# Export to Giotto
-def export_to_giotto(adata, output_dir):
-    import os
-    os.makedirs(output_dir, exist_ok=True)
-
-    # Expression matrix
-    pd.DataFrame(
-        adata.X.T,
-        index=adata.var_names,
-        columns=adata.obs_names
-    ).to_csv(f'{output_dir}/expression.csv')
-
-    # Cell coordinates
-    pd.DataFrame(
-        adata.obsm['spatial'],
-        columns=['x', 'y'],
-        index=adata.obs_names
-    ).to_csv(f'{output_dir}/spatial_locs.csv')
-
-# Export to Seurat
-def export_to_seurat(adata, output_file):
-    adata.write_h5ad(output_file)
-    # Read in R with: library(Seurat); ReadH5AD(output_file)
-```
-
-## Best Practices
-
-1. **Channel selection for segmentation:**
-   - Use brightest, most consistent nuclear marker (usually DAPI)
-   - Choose membrane/cytoplasm marker based on tissue type
-   - Test multiple options to optimize segmentation
-
-2. **Background subtraction:**
-   - Apply before quantification to reduce autofluorescence
-   - Use blank/control images to model background
-
-3. **Quality control:**
-   - Visualize segmentation on sample regions
-   - Check cell size distributions for outliers
-   - Validate marker expression ranges
-
-4. **Cell type annotation:**
-   - Start with canonical markers (CD3, CD20, panCK)
-   - Use multiple markers for robust classification
-   - Consider unsupervised clustering to discover populations
-
-5. **Spatial analysis:**
-   - Account for tissue architecture (epithelium, stroma, etc.)
-   - Consider local density when interpreting interactions
-   - Use permutation tests for statistical significance
-
-6. **Batch effects:**
-   - Include batch information in AnnData.obs
-   - Apply batch correction if combining multiple experiments
-   - Visualize batch effects with UMAP colored by batch
-
-## Common Issues and Solutions
-
-**Issue: Poor segmentation quality**
-- Verify nuclear and cytoplasm channels are correctly specified
-- Adjust image_resolution parameter to match actual resolution
-- Try different cytoplasm markers
-- Manually tune min/max cell size parameters
-
-**Issue: Low marker intensity**
-- Check for background subtraction artifacts
-- Verify channel names match actual channels
-- Inspect raw images for technical issues (focus, exposure)
-
-**Issue: Cell type annotations don't match expectations**
-- Adjust marker thresholds (too high/low)
-- Visualize marker distributions to set data-driven thresholds
-- Check for antibody specificity issues
-
-**Issue: Spatial analysis shows no significant interactions**
-- Increase neighborhood radius
-- Check for sufficient cell numbers per type
-- Verify spatial coordinates are correctly scaled
-
-## Additional Resources
-
-- **PathML Multiparametric API:** https://pathml.readthedocs.io/en/latest/api_multiparametric_reference.html
-- **CODEX:** https://www.akoyabio.com/codex/
-- **Vectra:** https://www.akoyabio.com/vectra/
-- **DeepCell Mesmer:** https://www.deepcell.org/
-- **Scanpy:** https://scanpy.readthedocs.io/ (single-cell analysis)
-- **Squidpy:** https://squidpy.readthedocs.io/ (spatial omics analysis)