torbcellselection
Filters and isolates T or B cell populations from mixed single-cell RNA sequencing data.
Install
mkdir -p .claude/skills/torbcellselection && curl -L -o skill.zip "https://agentskills.codes/api/skills/download/11487" && unzip -o skill.zip -d .claude/skills/torbcellselection && rm skill.zipInstalls to .claude/skills/torbcellselection
Activation
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Separates T and non-T cells or B and non-B cells from a mixed cell population. Uses either clonotype percentage from VDJ data, indicator gene expression (CD3 markers for T cells, CD19/CD20 for B cells), custom selector expressions, or k-means clustering for automatic selection.Key capabilities
- →Separate T cells from mixed cell populations.
- →Separate B cells from mixed cell populations.
- →Use clonotype percentage from VDJ data for cell selection.
- →Utilize indicator gene expression (e.g., CD3, CD19/CD20) for cell identification.
- →Apply k-means clustering for automatic cell selection when no custom selector is provided.
How it works
This skill separates T or B cells from mixed populations using VDJ clonotype data, marker gene expression, custom selector expressions, or k-means clustering. It processes Seurat objects and immune repertoire data to isolate relevant cell types for downstream analysis.
Inputs & outputs
When to use torbcellselection
- →Filtering T-cell clusters
- →Isolating B-cells
- →Preparing scRNA-seq data
- →Clonotype analysis
About this skill
TOrBCellSelection Process Configuration
Purpose
Separates T and non-T cells or B and non-B cells from a mixed cell population. Uses either clonotype percentage from VDJ data, indicator gene expression (CD3 markers for T cells, CD19/CD20 for B cells), custom selector expressions, or k-means clustering for automatic selection.
When to Use
- When dataset contains mixed cell types (T cells + other cell types, or B cells + other cell types)
- Before TCR-specific or BCR-specific analysis to isolate relevant cells
- After
SeuratClusteringOfAllCellsto identify which clusters are T/B cells - When scRNA-seq data includes scTCR-seq or scBCR-seq data
- DO NOT use if all cells in your dataset are already T/B cells
Configuration Structure
Process Enablement
[TOrBCellSelection]
cache = true # Enable caching for this process
Input Specification
[TOrBCellSelection.in]
# Seurat object file (RDS/qs2 format) from SeuratClusteringOfAllCells
srtobj = ["SeuratClusteringOfAllCells"]
# Optional: Immune repertoire data file (RDS/qs2 format) from ScRepLoading
# Required unless ignore_vdj is set to true
immdata = ["ScRepLoading"]
Environment Variables
[TOrBCellSelection.envs]
# Whether to ignore VDJ information and use only marker gene expression
ignore_vdj = false
# Custom R expression to identify T/B cells
# Example: "Clonotype_Pct > 0.25" selects cells with >25% clonotype percentage
# Can use indicator genes: "Clonotype_Pct > 0.25 & CD3E > 0"
# If not provided, k-means clustering will be used
selector = null
# List of indicator genes for T/B cell identification
# For T cells: ["CD3E", "CD3D", "CD3G"] (positive markers)
# or include negative markers: ["CD3E", "CD19", "CD14"]
# For B cells: ["CD19", "MS4A1", "CD79A", "CD79B"]
indicator_genes = ["CD3E"]
# Parameters for k-means clustering (if selector not provided)
# Reference: https://rdrr.io/r/stats/kmeans.html
# Note: dots in argument names should be replaced with hyphens
kmeans = {"nstart": 25}
Configuration Examples
Minimal Configuration (Default T Cell Markers)
[TOrBCellSelection]
[TOrBCellSelection.in]
srtobj = ["SeuratClusteringOfAllCells"]
What this does: Uses default CD3E marker + k-means clustering with VDJ data to automatically select T cell clusters.
T Cell Selection with Multiple CD3 Markers
[TOrBCellSelection]
[TOrBCellSelection.in]
srtobj = ["SeuratClusteringOfAllCells"]
immdata = ["ScRepLoading"]
[TOrBCellSelection.envs]
# Use all three CD3 markers for robust T cell identification
indicator_genes = ["CD3E", "CD3D", "CD3G"]
B Cell Selection (Default Markers)
[TOrBCellSelection]
[TOrBCellSelection.in]
srtobj = ["SeuratClusteringOfAllCells"]
immdata = ["ScRepLoading"]
[TOrBCellSelection.envs]
# Select B cells using CD19 and CD20 (MS4A1) markers
indicator_genes = ["CD19", "MS4A1"]
Selection by Clonotype Percentage Threshold
[TOrBCellSelection]
[TOrBCellSelection.in]
srtobj = ["SeuratClusteringOfAllCells"]
immdata = ["ScRepLoading"]
[TOrBCellSelection.envs]
# Select cells/clusters with >25% clonotype percentage as T/B cells
selector = "Clonotype_Pct > 0.25"
Selection Combined with Marker Expression
[TOrBCellSelection]
[TOrBCellSelection.in]
srtobj = ["SeuratClusteringOfAllCells"]
immdata = ["ScRepLoading"]
[TOrBCellSelection.envs]
# Select cells with high clonotype percentage AND CD3E expression
indicator_genes = ["CD3E"]
selector = "Clonotype_Pct > 0.25 & CD3E > 0"
Selection Without VDJ Data (Markers Only)
[TOrBCellSelection]
[TOrBCellSelection.in]
srtobj = ["SeuratClusteringOfAllCells"]
[TOrBCellSelection.envs]
# Ignore VDJ data, use only marker gene expression
ignore_vdj = true
# Need at least 2 markers for k-means when VDJ is ignored
indicator_genes = ["CD3E", "CD3D", "CD3G"]
# First gene must be a positive marker for selection
# (CD3E is positive for T cells)
B Cell Selection Without VDJ Data
[TOrBCellSelection]
[TOrBCellSelection.in]
srtobj = ["SeuratClusteringOfAllCells"]
[TOrBCellSelection.envs]
# Select B cells using markers only (no VDJ data)
ignore_vdj = true
indicator_genes = ["CD19", "MS4A1", "CD79A"]
Custom K-means Parameters
[TOrBCellSelection]
[TOrBCellSelection.in]
srtobj = ["SeuratClusteringOfAllCells"]
immdata = ["ScRepLoading"]
[TOrBCellSelection.envs]
indicator_genes = ["CD3E", "CD3D", "CD3G"]
# Custom k-means parameters
# nstart: number of random starts for stability (default: 25)
# iter.max: maximum iterations (default: 10 in R)
# Note: hyphens instead of dots in key names
kmeans = {"nstart": 50, "iter-max": 20}
Common Patterns
Pattern 1: Standard T Cell Selection (with VDJ)
[TOrBCellSelection]
[TOrBCellSelection.in]
srtobj = ["SeuratClusteringOfAllCells"]
immdata = ["ScRepLoading"]
[TOrBCellSelection.envs]
# Robust T cell selection using all three CD3 markers
indicator_genes = ["CD3E", "CD3D", "CD3G"]
When to use: Typical TCR-seq analysis where T cells need to be separated from other cell types.
Pattern 2: Standard B Cell Selection (with VDJ)
[TOrBCellSelection]
[TOrBCellSelection.in]
srtobj = ["SeuratClusteringOfAllCells"]
immdata = ["ScRepLoading"]
[TOrBCellSelection.envs]
# B cell selection using CD19 and CD20 markers
indicator_genes = ["CD19", "MS4A1"]
When to use: BCR-seq analysis where B cells need to be separated from other cell types.
Pattern 3: High-Sensitivity T Cell Selection
[TOrBCellSelection]
[TOrBCellSelection.in]
srtobj = ["SeuratClusteringOfAllCells"]
immdata = ["ScRepLoading"]
[TOrBCellSelection.envs]
# Lower threshold to capture more T cells
selector = "Clonotype_Pct > 0.10 & CD3E > 0"
When to use: When you suspect low-quality VDJ data or want to capture borderline T cells.
Pattern 4: High-Specificity T Cell Selection
[TOrBCellSelection]
[TOrBCellSelection.in]
srtobj = ["SeuratClusteringOfAllCells"]
immdata = ["ScRepLoading"]
[TOrBCellSelection.envs]
# Higher threshold for clean T cell population
selector = "Clonotype_Pct > 0.50 & CD3E > 1"
When to use: When you want only the highest-confidence T cells (e.g., for clonal expansion analysis).
Pattern 5: Auto-Selection (K-means) with Multiple Markers
[TOrBCellSelection]
[TOrBCellSelection.in]
srtobj = ["SeuratClusteringOfAllCells"]
immdata = ["ScRepLoading"]
[TOrBCellSelection.envs]
# Let k-means determine T cell clusters automatically
# No selector = automatic selection
indicator_genes = ["CD3E", "CD3D", "CD3G"]
kmeans = {"nstart": 50}
When to use: When you don't have a specific threshold in mind and want automatic unsupervised selection.
Dependencies
Upstream Processes
- SeuratClusteringOfAllCells: Provides clustered Seurat object with
seurat_clustersmetadata - ScRepLoading: Provides VDJ data with clonotype information (unless
ignore_vdj = true)
Downstream Processes
- SeuratClustering: Clusters the selected T/B cells for downstream analysis
- ScRepCombiningExpression: Combines selected cells with VDJ data
- ModuleScoreCalculator: Calculates module scores on selected cells
- Other TCR/BCR-specific processes (CDR3Clustering, TESSA, ClonalStats, etc.)
Workflow Integration
SeuratPreparing → SeuratClusteringOfAllCells → TOrBCellSelection → SeuratClustering → (downstream TCR/BCR analysis)
↑
ScRepLoading
Selection Methods Explained
Method 1: K-means Clustering (Default)
When selector is not provided, TOrBCellSelection performs:
- Calculates average expression of indicator genes per cluster
- If VDJ data available: calculates clonotype percentage per cluster
- Performs k-means clustering (K=2) on [gene expressions + clonotype_pct]
- Selects cluster with higher clonotype percentage (or higher expression of first indicator gene if no VDJ)
Pros: Automatic, unsupervised, adapts to data Cons: May select unexpected clusters if data is noisy
Method 2: Custom Selector Expression
Provide a custom R expression via selector:
- Can use any metadata column:
Clonotype_Pct > 0.25 - Can combine with gene expression:
Clonotype_Pct > 0.25 & CD3E > 0 - Can use complex logic:
(Clonotype_Pct > 0.25 | CD3E > 1) & CD19 < 0.1
Pros: Full control, transparent selection criteria Cons: Requires domain knowledge, need to test thresholds
Method 3: Marker-Only Selection (ignore_vdj)
Set ignore_vdj = true to use only marker genes:
- Useful when VDJ data is poor or missing
- Requires at least 2 indicator genes for k-means
- First gene in list must be positive marker for the target cell type
Pros: Works without VDJ data, robust marker-based selection Cons: Requires good marker genes, may include non-clonal cells
Marker Gene Recommendations
T Cell Markers
Positive markers (expressed in T cells):
CD3E: Core CD3 epsilon chain (most reliable)CD3D: Core CD3 delta chainCD3G: Core CD3 gamma chain
Negative markers (excluded from T cells):
CD19: B cell markerMS4A1(CD20): B cell markerCD14: Monocyte markerCD68: Macrophage marker
Recommended for T cells:
indicator_genes = ["CD3E", "CD3D", "CD3G"]
B Cell Markers
Positive markers (expressed in B cells):
CD19: Pan-B cell marker (most reliable)MS4A1(CD20): Mature B cell markerCD79A: B cell receptor componentCD79B: B cell receptor component
Recommended for B cells:
indicator_genes = ["CD19", "MS4A1"]
Subtype-Specific Markers
For selecting specific T/B cell subtypes:
- T helper cells:
CD4 - Cytotoxic T cells:
CD8A,CD8B - Regulatory T cells:
FOXP3,IL2RA - Memory B cells:
CD27 - Plasma cells:
CD38,SDC1(CD138)
Validation Rules
Required Inputs
srtobjmust be specified (from SeuratCl
Content truncated.
When not to use it
- →If all cells in the dataset are already T/B cells.
- →If the dataset does not contain mixed cell types (T cells + other, or B cells + other).
Limitations
- →Selection happens at the cluster level, not single-cell level.
- →Gene expression values are normalized (mean=0, SD=1) before k-means clustering.
- →When using k-means without VDJ data, the first indicator gene must be a positive marker for the target cell type.
How it compares
This skill automates the complex process of immune cell subset selection based on various biological markers and data types, providing a structured and configurable approach compared to manual gating or less integrated methods.
Compared to similar skills
torbcellselection side by side with the closest alternatives in the catalog.
| Skill | Installs | Updated | Safety | Difficulty |
|---|---|---|---|---|
| torbcellselection (this skill) | 0 | 6mo | Review | Advanced |
| quant-analyst | 103 | 2mo | No flags | Advanced |
| umap-learn | 6 | 2mo | Review | Intermediate |
| embedding-strategies | 8 | 2mo | No flags | Intermediate |
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