xiaohongshu
xiaohongshu
bio-single-cell-cell-annotation
Automated cell type annotation using reference-based methods including CellTypist, scPred, SingleR, and Azimuth for consistent, reproducible cell labeling. Use when automatically annotating cell types using reference datasets.
Full skill instructions
import celltypist
import scanpy as sc
adata = sc.read_h5ad('adata_processed.h5ad')
# List available models
celltypist.models.models_description()
# Download model
celltypist.models.download_models(model='Immune_All_Low.pkl')
# Load model
model = celltypist.models.Model.load(model='Immune_All_Low.pkl')
# Predict cell types
predictions = celltypist.annotate(adata, model=model, majority_voting=True)
# Add predictions to adata
adata = predictions.to_adata()
# Access predictions
adata.obs['cell_type_celltypist'] = adata.obs['majority_voting']
adata.obs['cell_type_confidence'] = adata.obs['conf_score']
# Visualize
sc.pl.umap(adata, color=['cell_type_celltypist', 'conf_score'])
# Train custom model
new_model = celltypist.train(adata_reference, labels='cell_type', n_jobs=10,
feature_selection=True, use_SGD=True)
# Save model
new_model.write('custom_model.pkl')
# Use custom model
predictions = celltypist.annotate(adata_query, model='custom_model.pkl')
library(SingleR)
library(celldex)
library(Seurat)
library(SingleCellExperiment)
seurat_obj <- readRDS('seurat_processed.rds')
sce <- as.SingleCellExperiment(seurat_obj)
# Load reference (multiple available)
ref <- celldex::HumanPrimaryCellAtlasData()
# Other options:
# ref <- celldex::BlueprintEncodeData()
# ref <- celldex::MonacoImmuneData()
# ref <- celldex::ImmGenData() # mouse
# Run SingleR
pred <- SingleR(test = sce, ref = ref, labels = ref$label.main, de.method = 'wilcox')
# Add to Seurat
seurat_obj$SingleR_labels <- pred$labels
seurat_obj$SingleR_pruned <- pred$pruned.labels
# Check annotation quality
plotScoreHeatmap(pred)
plotDeltaDistribution(pred)
# Use fine-grained labels
pred_fine <- SingleR(test = sce, ref = ref, labels = ref$label.fine)
# Combine multiple references
ref1 <- celldex::BlueprintEncodeData()
ref2 <- celldex::MonacoImmuneData()
pred_combined <- SingleR(test = sce, ref = list(BP = ref1, Monaco = ref2),
labels = list(ref1$label.main, ref2$label.main))
library(Seurat)
library(Azimuth)
seurat_obj <- readRDS('seurat_processed.rds')
# Run Azimuth with PBMC reference
seurat_obj <- RunAzimuth(seurat_obj, reference = 'pbmcref')
# Available references: pbmcref, bonemarrowref, lungref, etc.
# Access predictions
seurat_obj$azimuth_labels <- seurat_obj$predicted.celltype.l2
seurat_obj$azimuth_score <- seurat_obj$predicted.celltype.l2.score
# Visualize
DimPlot(seurat_obj, group.by = 'azimuth_labels', label = TRUE) + NoLegend()
FeaturePlot(seurat_obj, features = 'predicted.celltype.l2.score')
library(scPred)
library(Seurat)
# Train on reference
reference <- readRDS('reference_seurat.rds')
reference <- getFeatureSpace(reference, 'cell_type')
reference <- trainModel(reference)
# Get training probabilities
get_probabilities(reference)
get_scpred(reference)
# Plot model performance
plot_probabilities(reference)
# Predict on query
query <- readRDS('query_seurat.rds')
query <- scPredict(query, reference)
# Results
query$scpred_prediction
query$scpred_max
# CellTypist: filter low confidence
high_conf = adata[adata.obs['conf_score'] > 0.5].copy()
# Flag uncertain cells
adata.obs['annotation_uncertain'] = adata.obs['conf_score'] < 0.3
# SingleR: use pruned labels (low-quality removed)
seurat_obj$final_labels <- ifelse(is.na(pred$pruned.labels), 'Unknown', pred$labels)
# Azimuth: filter by score
seurat_obj$high_conf_labels <- ifelse(seurat_obj$predicted.celltype.l2.score > 0.7,
seurat_obj$predicted.celltype.l2, 'Low_confidence')
# Combine multiple methods
annotations <- data.frame(
SingleR = seurat_obj$SingleR_labels,
Azimuth = seurat_obj$azimuth_labels,
CellTypist = seurat_obj$celltypist_labels
)
# Majority vote
get_consensus <- function(x) {
tbl <- table(x)
if (max(tbl) >= 2) names(which.max(tbl)) else 'Ambiguous'
}
seurat_obj$consensus_label <- apply(annotations, 1, get_consensus)
import pandas as pd
from sklearn.metrics import adjusted_rand_score, normalized_mutual_info_score
# Compare two annotations
ari = adjusted_rand_score(adata.obs['manual_annotation'], adata.obs['celltypist'])
nmi = normalized_mutual_info_score(adata.obs['manual_annotation'], adata.obs['celltypist'])
# Confusion matrix
pd.crosstab(adata.obs['manual_annotation'], adata.obs['celltypist'])
# Validate predictions with known markers
canonical_markers <- list(
T_cell = c('CD3D', 'CD3E', 'CD4', 'CD8A'),
B_cell = c('CD19', 'MS4A1', 'CD79A'),
Monocyte = c('CD14', 'LYZ', 'S100A8'),
NK = c('NKG7', 'GNLY', 'NCAM1')
)
# Check marker expression per predicted type
DotPlot(seurat_obj, features = unlist(canonical_markers), group.by = 'predicted_labels') +
RotatedAxis()
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