git clone https://github.com/mdbabumiamssm/LLMs-Universal-Life-Science-and-Clinical-Skills-
T=$(mktemp -d) && git clone --depth=1 https://github.com/mdbabumiamssm/LLMs-Universal-Life-Science-and-Clinical-Skills- "$T" && mkdir -p ~/.claude/skills && cp -r "$T/Skills/Genomics/Single_Cell/doublet-detection" ~/.claude/skills/mdbabumiamssm-llms-universal-life-science-and-clinical-skills-doublet-detection-081629 && rm -rf "$T"
Skills/Genomics/Single_Cell/doublet-detection/SKILL.mdname: bio-single-cell-doublet-detection description: Detect and remove doublets (multiple cells captured in one droplet) from single-cell RNA-seq data. Uses Scrublet (Python), DoubletFinder (R), and scDblFinder (R). Essential QC step before clustering to avoid artificial cell populations. Use when identifying and removing doublets from scRNA-seq data. tool_type: mixed primary_tool: Scrublet measurable_outcome: Execute skill workflow successfully with valid output within 15 minutes. allowed-tools:
- read_file
- run_shell_command
Doublet Detection
Doublets are droplets containing two or more cells. They appear as artificial intermediate cell populations and must be removed before analysis.
Scrublet (Python)
Fast doublet detection based on simulated doublets from the data.
Basic Usage
import scrublet as scr import scanpy as sc import numpy as np adata = sc.read_10x_mtx('filtered_feature_bc_matrix/') scrub = scr.Scrublet(adata.X, expected_doublet_rate=0.06) doublet_scores, predicted_doublets = scrub.scrub_doublets() adata.obs['doublet_score'] = doublet_scores adata.obs['predicted_doublet'] = predicted_doublets print(f'Detected {predicted_doublets.sum()} doublets ({100*predicted_doublets.mean():.1f}%)')
Adjust Parameters
scrub = scr.Scrublet(adata.X, expected_doublet_rate=0.06) doublet_scores, predicted_doublets = scrub.scrub_doublets( min_counts=2, min_cells=3, min_gene_variability_pctl=85, n_prin_comps=30, synthetic_doublet_umi_subsampling=1.0 )
Visualize Doublet Scores
import matplotlib.pyplot as plt scrub.plot_histogram() plt.savefig('doublet_histogram.pdf') # UMAP with doublet scores sc.pp.normalize_total(adata, target_sum=1e4) sc.pp.log1p(adata) sc.pp.highly_variable_genes(adata) sc.pp.pca(adata) sc.pp.neighbors(adata) sc.tl.umap(adata) sc.pl.umap(adata, color=['doublet_score', 'predicted_doublet'], save='_doublets.pdf')
Filter Doublets
adata_filtered = adata[~adata.obs['predicted_doublet']].copy() print(f'Kept {adata_filtered.n_obs} cells after doublet removal')
Set Manual Threshold
scrub = scr.Scrublet(adata.X) doublet_scores, _ = scrub.scrub_doublets() threshold = 0.25 predicted_doublets = doublet_scores > threshold adata.obs['predicted_doublet'] = predicted_doublets
DoubletFinder (R)
Popular R package for doublet detection in Seurat workflows.
Basic Usage
library(Seurat) library(DoubletFinder) seurat_obj <- Read10X(data.dir = 'filtered_feature_bc_matrix/') seurat_obj <- CreateSeuratObject(counts = seurat_obj, min.cells = 3, min.features = 200) seurat_obj <- NormalizeData(seurat_obj) seurat_obj <- FindVariableFeatures(seurat_obj) seurat_obj <- ScaleData(seurat_obj) seurat_obj <- RunPCA(seurat_obj) seurat_obj <- RunUMAP(seurat_obj, dims = 1:20) seurat_obj <- FindNeighbors(seurat_obj, dims = 1:20) seurat_obj <- FindClusters(seurat_obj, resolution = 0.5) sweep.res <- paramSweep(seurat_obj, PCs = 1:20, sct = FALSE) sweep.stats <- summarizeSweep(sweep.res, GT = FALSE) bcmvn <- find.pK(sweep.stats) optimal_pk <- as.numeric(as.character(bcmvn$pK[which.max(bcmvn$BCmetric)])) nExp_poi <- round(0.06 * nrow(seurat_obj@meta.data)) seurat_obj <- doubletFinder(seurat_obj, PCs = 1:20, pN = 0.25, pK = optimal_pk, nExp = nExp_poi, reuse.pANN = FALSE, sct = FALSE) colnames(seurat_obj@meta.data)
With SCTransform
seurat_obj <- SCTransform(seurat_obj) seurat_obj <- RunPCA(seurat_obj) seurat_obj <- RunUMAP(seurat_obj, dims = 1:30) seurat_obj <- FindNeighbors(seurat_obj, dims = 1:30) seurat_obj <- FindClusters(seurat_obj, resolution = 0.5) sweep.res <- paramSweep(seurat_obj, PCs = 1:30, sct = TRUE) sweep.stats <- summarizeSweep(sweep.res, GT = FALSE) bcmvn <- find.pK(sweep.stats) optimal_pk <- as.numeric(as.character(bcmvn$pK[which.max(bcmvn$BCmetric)])) nExp_poi <- round(0.06 * nrow(seurat_obj@meta.data)) seurat_obj <- doubletFinder(seurat_obj, PCs = 1:30, pN = 0.25, pK = optimal_pk, nExp = nExp_poi, reuse.pANN = FALSE, sct = TRUE)
Filter Doublets
df_col <- grep('DF.classifications', colnames(seurat_obj@meta.data), value = TRUE) seurat_obj$doublet <- seurat_obj@meta.data[[df_col]] DimPlot(seurat_obj, group.by = 'doublet') seurat_obj <- subset(seurat_obj, subset = doublet == 'Singlet')
Adjust Expected Doublet Rate
n_cells <- ncol(seurat_obj) doublet_rate <- n_cells / 1000 * 0.008 nExp_poi <- round(doublet_rate * n_cells)
scDblFinder (R/Bioconductor)
Fast Bioconductor package using gradient boosting for doublet detection.
Basic Usage
library(scDblFinder) library(SingleCellExperiment) sce <- SingleCellExperiment(assays = list(counts = counts_matrix)) sce <- scDblFinder(sce) table(sce$scDblFinder.class)
From Seurat Object
library(scDblFinder) library(Seurat) sce <- as.SingleCellExperiment(seurat_obj) sce <- scDblFinder(sce) seurat_obj$scDblFinder_class <- sce$scDblFinder.class seurat_obj$scDblFinder_score <- sce$scDblFinder.score DimPlot(seurat_obj, group.by = 'scDblFinder_class') seurat_obj <- subset(seurat_obj, subset = scDblFinder_class == 'singlet')
Multi-Sample Processing
sce <- scDblFinder(sce, samples = 'sample_id')
Adjust Parameters
sce <- scDblFinder(sce, dbr = 0.06, dbr.sd = 0.015, nfeatures = 1500, dims = 20, k = 30 )
Expected Doublet Rates
| Cells Loaded | Expected Rate |
|---|---|
| 1,000 | ~0.8% |
| 2,000 | ~1.6% |
| 5,000 | ~4.0% |
| 10,000 | ~8.0% |
| 15,000 | ~12% |
Formula:
rate ≈ cells_loaded / 1000 * 0.008
Compare Methods
library(scDblFinder) seurat_obj$scrublet <- scrublet_results sce <- as.SingleCellExperiment(seurat_obj) sce <- scDblFinder(sce) seurat_obj$scDblFinder <- sce$scDblFinder.class DimPlot(seurat_obj, group.by = c('doublet', 'scDblFinder', 'scrublet'), ncol = 3) table(seurat_obj$doublet, seurat_obj$scDblFinder)
Handling Heterotypic vs Homotypic Doublets
Heterotypic Doublets
- Two different cell types
- Easier to detect (intermediate expression)
- All methods handle well
Homotypic Doublets
- Same cell type
- Harder to detect (no intermediate signature)
- May have higher total counts
adata.obs['log_counts'] = np.log1p(adata.obs['total_counts']) sc.pl.violin(adata, 'log_counts', groupby='predicted_doublet')
Scanpy Integration Pipeline
import scanpy as sc import scrublet as scr adata = sc.read_10x_mtx('filtered_feature_bc_matrix/') adata.var['mt'] = adata.var_names.str.startswith('MT-') sc.pp.calculate_qc_metrics(adata, qc_vars=['mt'], inplace=True) scrub = scr.Scrublet(adata.X, expected_doublet_rate=0.06) doublet_scores, predicted_doublets = scrub.scrub_doublets() adata.obs['doublet_score'] = doublet_scores adata.obs['is_doublet'] = predicted_doublets print(f'Before filtering: {adata.n_obs} cells') adata = adata[~adata.obs['is_doublet']].copy() adata = adata[adata.obs['pct_counts_mt'] < 20].copy() print(f'After filtering: {adata.n_obs} cells') sc.pp.normalize_total(adata, target_sum=1e4) sc.pp.log1p(adata) sc.pp.highly_variable_genes(adata) sc.pp.pca(adata) sc.pp.neighbors(adata) sc.tl.umap(adata) sc.tl.leiden(adata)
Seurat Integration Pipeline
library(Seurat) library(DoubletFinder) seurat_obj <- Read10X('filtered_feature_bc_matrix/') seurat_obj <- CreateSeuratObject(counts = seurat_obj, min.cells = 3, min.features = 200) seurat_obj[['percent.mt']] <- PercentageFeatureSet(seurat_obj, pattern = '^MT-') seurat_obj <- NormalizeData(seurat_obj) seurat_obj <- FindVariableFeatures(seurat_obj) seurat_obj <- ScaleData(seurat_obj) seurat_obj <- RunPCA(seurat_obj) seurat_obj <- RunUMAP(seurat_obj, dims = 1:20) seurat_obj <- FindNeighbors(seurat_obj, dims = 1:20) seurat_obj <- FindClusters(seurat_obj, resolution = 0.5) sweep.res <- paramSweep(seurat_obj, PCs = 1:20) sweep.stats <- summarizeSweep(sweep.res) bcmvn <- find.pK(sweep.stats) pk <- as.numeric(as.character(bcmvn$pK[which.max(bcmvn$BCmetric)])) nExp <- round(0.06 * ncol(seurat_obj)) seurat_obj <- doubletFinder(seurat_obj, PCs = 1:20, pN = 0.25, pK = pk, nExp = nExp) df_col <- grep('DF.classifications', colnames(seurat_obj@meta.data), value = TRUE) seurat_obj <- subset(seurat_obj, cells = colnames(seurat_obj)[seurat_obj@meta.data[[df_col]] == 'Singlet']) seurat_obj <- subset(seurat_obj, subset = percent.mt < 20) seurat_obj <- NormalizeData(seurat_obj) seurat_obj <- FindVariableFeatures(seurat_obj) seurat_obj <- ScaleData(seurat_obj) seurat_obj <- RunPCA(seurat_obj) seurat_obj <- RunUMAP(seurat_obj, dims = 1:20) seurat_obj <- FindNeighbors(seurat_obj, dims = 1:20) seurat_obj <- FindClusters(seurat_obj)
Method Comparison
| Method | Speed | Accuracy | Language |
|---|---|---|---|
| Scrublet | Fast | Good | Python |
| DoubletFinder | Slow | Good | R |
| scDblFinder | Fast | Excellent | R |
Related Skills
- preprocessing - QC before doublet detection
- clustering - Run after filtering doublets
- data-io - Load data before processing