Workflow for read alignment, sorting, indexing, mapping statistics, and downstream-ready alignment artifacts.
日本語の概要は準備中です。原文の説明を表示しています。
Maps query single-cell data to reference atlases using scArches transfer learning with scVI and scANVI models. Transfers cell type labels without retraining on combined data. Use when annotating new single-cell datasets using pre-trained reference models.
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Reference examples tested with: anndata 0.10+, scanpy 1.10+, scvi-tools 1.1+
Before using code patterns, verify installed versions match. If versions differ:
pip show <package> then help(module.function) to check signaturesIf code throws ImportError, AttributeError, or TypeError, introspect the installed package and adapt the example to match the actual API rather than retrying.
"Map my scRNA-seq data onto a reference atlas" → Transfer cell type labels from a pre-trained reference model to query cells using architectural surgery (scArches) without retraining.
scvi.model.SCVI.load_query_data() → get_latent_representation() → scanpy.tl.ingest()Goal: Map query single-cell data onto a pre-trained reference model to obtain a shared latent embedding.
Approach: Load a pre-trained scVI model, prepare query data with matching gene sets, then perform surgical fine-tuning that updates only query-specific parameters.
import scvi
import scanpy as sc
# Load pre-trained reference model
adata_ref = sc.read_h5ad('reference.h5ad')
# Model must have been saved with save_anndata=True
scvi.model.SCVI.setup_anndata(adata_ref, layer='counts', batch_key='batch')
ref_model = scvi.model.SCVI.load('reference_model/', adata=adata_ref)
# Prepare query data
adata_query = sc.read_h5ad('query.h5ad')
# Subset to reference genes
adata_query = adata_query[:, adata_ref.var_names].copy()
# Set up query AnnData using reference setup
scvi.model.SCVI.prepare_query_anndata(adata_query, ref_model)
# Load query into model (creates "surgical" fine-tuned model)
query_model = scvi.model.SCVI.load_query_data(adata_query, ref_model)
# Surgical training: update only query-specific parameters
# weight_decay=0.0: Standard for surgery; prevents reference drift
query_model.train(max_epochs=200, plan_kwargs={'weight_decay': 0.0})
# Get latent representation
adata_query.obsm['X_scVI'] = query_model.get_latent_representation()
Goal: Transfer cell type labels from a labeled reference atlas to unlabeled query data.
Approach: Train a semi-supervised scANVI model on the reference, then map query cells via surgical fine-tuning and predict labels with confidence scores.
import scvi
import scanpy as sc
# Reference with cell type labels
adata_ref = sc.read_h5ad('reference_labeled.h5ad')
scvi.model.SCVI.setup_anndata(adata_ref, layer='counts', batch_key='batch')
ref_vae = scvi.model.SCVI(adata_ref, n_latent=30)
ref_vae.train(max_epochs=100)
# Convert to scANVI (semi-supervised)
scvi.model.SCANVI.setup_anndata(adata_ref, layer='counts', batch_key='batch', labels_key='cell_type', unlabeled_category='Unknown')
ref_scanvi = scvi.model.SCANVI.from_scvi_model(ref_vae, labels_key='cell_type', unlabeled_category='Unknown')
ref_scanvi.train(max_epochs=50)
ref_scanvi.save('reference_scanvi/')
# Map query data
adata_query = sc.read_h5ad('query.h5ad')
adata_query = adata_query[:, adata_ref.var_names].copy()
scvi.model.SCANVI.prepare_query_anndata(adata_query, ref_scanvi)
query_scanvi = scvi.model.SCANVI.load_query_data(adata_query, ref_scanvi)
query_scanvi.train(max_epochs=100, plan_kwargs={'weight_decay': 0.0})
# Transfer labels
adata_query.obs['predicted_cell_type'] = query_scanvi.predict()
adata_query.obsm['X_scANVI'] = query_scanvi.get_latent_representation()
Goal: Assess reliability of transferred labels and flag cells that may represent novel types.
Approach: Extract soft prediction probabilities from the scANVI model and identify low-confidence assignments below a threshold.
# Get prediction probabilities
soft_predictions = query_scanvi.predict(soft=True)
adata_query.obs['prediction_confidence'] = soft_predictions.max(axis=1)
# Flag low-confidence predictions
# confidence < 0.5: May be novel cell type or poor mapping
low_conf = adata_query.obs['prediction_confidence'] < 0.5
print(f'Low confidence predictions: {low_conf.sum()} ({low_conf.mean():.1%})')
Goal: Visualize reference and query cells together to assess integration quality.
Approach: Concatenate reference and query datasets, compute UMAP from the shared latent representation, and color by dataset and cell type.
import scanpy as sc
# Combine reference and query for visualization
adata_combined = adata_ref.concatenate(adata_query, batch_key='dataset', batch_categories=['reference', 'query'])
# Use latent space for neighbors/UMAP
sc.pp.neighbors(adata_combined, use_rep='X_scVI')
sc.tl.umap(adata_combined)
sc.pl.umap(adata_combined, color=['dataset', 'cell_type'], save='_transfer.png')
| Atlas | Model | URL |
|---|---|---|
| Human Lung Cell Atlas | scANVI | cellxgene.cziscience.com |
| Tabula Sapiens | scVI | tabula-sapiens-portal.ds.czbiohub.org |
| Mouse Cell Atlas | scVI | bis.zju.edu.cn/MCA |
| Parameter | Surgical | Full Retrain | Notes |
|---|---|---|---|
| weight_decay | 0.0 | 0.001 | 0.0 preserves reference |
| max_epochs | 100-200 | 200-400 | Less for surgery |
| early_stopping | True | True | Prevents overfitting |
まだレビューはありません。使ってみた感想をお寄せください。
概要と使いどころ
Workflow for read alignment, sorting, indexing, mapping statistics, and downstream-ready alignment artifacts.
日本語の概要は準備中です。原文の説明を表示しています。
Validate protein designs using AlphaFold2 structure prediction. Use this skill when: (1) Validating designed sequences fold correctly, (2) Predicting binder-target complex structures, (3) Calculating confidence metrics (pLDDT, pTM, ipTM), (4) Self-consistency validation of designs, (5) Multi-chain complex prediction with AlphaFold-Multimer. For faster single-chain prediction, use esm. For QC thresholds, use protein-qc.
日本語の概要は準備中です。原文の説明を表示しています。
AlphaFold2 / AlphaFold-Multimer structure prediction for validation and confidence scoring. Use this skill when: (1) Validating designed sequences fold correctly, (2) Predicting binder-target complex structures, (3) Calculating confidence metrics (pLDDT, pTM, ipTM), (4) Self-consistency validation of designs, (5) Multi-chain complex prediction with AlphaFold-Multimer. For faster single-chain prediction, use esm2-sequence-scoring. For QC thresholds, use protein-design-qc.
日本語の概要は準備中です。原文の説明を表示しています。
Workflow for event-level and isoform-level splicing analysis with sashimi-ready outputs and splice QC.
日本語の概要は準備中です。原文の説明を表示しています。
ATAC-seq processing with assay QC, MACS3 peak calling, consensus peak matrices, differential accessibility, and motif or footprint follow-up.
日本語の概要は準備中です。原文の説明を表示しています。
End-to-end binder design using BindCraft hallucination. Use this skill when: (1) Designing protein binders with built-in AF2 validation, (2) Running production-quality binder campaigns, (3) Using different design protocols (fast, default, slow), (4) Need joint backbone and sequence optimization, (5) Want high experimental success rate. For backbone-only generation, use rfdiffusion. For QC thresholds, use protein-qc. For tool selection guidance, use binder-design.
日本語の概要は準備中です。原文の説明を表示しています。