cellxgene-census — Централизованный доступ к данным секвенирования единичных клеток

--- name: cellxgene-census description: Query the CELLxGENE Census (61M+ cells) programmatically. Use when you need expression data across tissues, diseases, or cell types from the largest curated single-cell atlas. Best for population-scale queries, reference atlas comparisons. For analyzing your own data use scanpy or scvi-tools. license: Unknown metadata: skill-author: K-Dense Inc. --- # CZ CELLxGENE Census ## Overview The CZ CELLxGENE Census provides programmatic access to a comprehensive, versioned collection of standardized single-cell genomics data from CZ CELLxGENE Discover. This skill enables efficient querying and analysis of millions of cells across thousands of datasets. The Census includes: - **61+ million cells** from human and mouse - **Standardized metadata** (cell types, tissues, diseases, donors) - **Raw gene expression** matrices - **Pre-calculated embeddings** and statistics - **Integration with PyTorch, scanpy, and other analysis tools** ## When to Use This Skill This skill should be used when: - Querying single-cell expression data by cell type, tissue, or disease - Exploring available single-cell datasets and metadata - Training machine learning models on single-cell data - Performing large-scale cross-dataset analyses - Integrating Census data with scanpy or other analysis frameworks - Computing statistics across millions of cells - Accessing pre-calculated embeddings or model predictions ## Installation and Setup Install the Census API: ```bash uv pip install cellxgene-census ``` For machine learning workflows, install additional dependencies: ```bash uv pip install cellxgene-census[experimental] ``` ## Core Workflow Patterns ### 1. Opening the Census Always use the context manager to ensure proper resource cleanup: ```python import cellxgene_census # Open latest stable version with cellxgene_census.open_soma() as census: # Work with census data # Open specific version for reproducibility with cellxgene_census.open_soma(census_version="2023-07-25") as census: # Work with census data ``` **Key points:** - Use context manager (`with` statement) for automatic cleanup - Specify `census_version` for reproducible analyses - Default opens latest "stable" release ### 2. Exploring Census Information Before querying expression data, explore available datasets and metadata. **Access summary information:** ```python # Get summary statistics summary = census["census_info"]["summary"].read().concat().to_pandas() print(f"Total cells: {summary['total_cell_count'][0]}") # Get all datasets datasets = census["census_info"]["datasets"].read().concat().to_pandas() # Filter datasets by criteria covid_datasets = datasets[datasets["disease"].str.contains("COVID", na=False)] ``` **Query cell metadata to understand available data:** ```python # Get unique cell types in a tissue cell_metadata = cellxgene_census.get_obs( census, "homo_sapiens", value_filter="tissue_general == 'brain' and is_primary_data == True", column_names=["cell_type"] ) unique_cell_types = cell_metadata["cell_type"].unique() print(f"Found {len(unique_cell_types)} cell types in brain") # Count cells by tissue tissue_counts = cell_metadata.groupby("tissue_general").size() ``` **Important:** Always filter for `is_primary_data == True` to avoid counting duplicate cells unless specifically analyzing duplicates. ### 3. Querying Expression Data (Small to Medium Scale) For queries returning < 100k cells that fit in memory, use `get_anndata()`: ```python # Basic query with cell type and tissue filters adata = cellxgene_census.get_anndata( census=census, organism="Homo sapiens", # or "Mus musculus" obs_value_filter="cell_type == 'B cell' and tissue_general == 'lung' and is_primary_data == True", obs_column_names=["assay", "disease", "sex", "donor_id"], ) # Query specific genes with multiple filters adata = cellxgene_census.get_anndata( census=census, organism="Homo sapiens", var_value_filter="feature_name in ['CD4', 'CD8A', 'CD19', 'FOXP3']", obs_value_filter="cell_type == 'T cell' and disease == 'COVID-19' and is_primary_data == True", obs_column_names=["cell_type", "tissue_general", "donor_id"], ) ``` **Filter syntax:** - Use `obs_value_filter` for cell filtering - Use `var_value_filter` for gene filtering - Combine conditions with `and`, `or` - Use `in` for multiple values: `tissue in ['lung', 'liver']` - Select only needed columns with `obs_column_names` **Getting metadata separately:** ```python # Query cell metadata cell_metadata = cellxgene_census.get_obs( census, "homo_sapiens", value_filter="disease == 'COVID-19' and is_primary_data == True", column_names=["cell_type", "tissue_general", "donor_id"] ) # Query gene metadata gene_metadata = cellxgene_census.get_var( census, "homo_sapiens", value_filter="feature_name in ['CD4', 'CD8A']", column_names=["feature_id", "feature_name", "feature_length"] ) ``` ### 4. Large-Scale Queries (Out-of-Core Processing) For queries exceeding available RAM, use `axis_query()` with iterative processing: ```python import tiledbsoma as soma # Create axis query query = census["census_data"]["homo_sapiens"].axis_query( measurement_name="RNA", obs_query=soma.AxisQuery( value_filter="tissue_general == 'brain' and is_primary_data == True" ), var_query=soma.AxisQuery( value_filter="feature_name in ['FOXP2', 'TBR1', 'SATB2']" ) ) # Iterate through expression matrix in chunks iterator = query.X("raw").tables() for batch in iterator: # batch is a pyarrow.Table with columns: # - soma_data: expression value # - soma_dim_0: cell (obs) coordinate # - soma_dim_1: gene (var) coordinate process_batch(batch) ``` **Computing incremental statistics:** ```python # Example: Calculate mean expression n_observations = 0 sum_values = 0.0 iterator = query.X("raw").tables() for batch in iterator: values = batch["soma_data"].to_numpy() n_observations += len(values) sum_values += values.sum() mean_expression = sum_values / n_observations ``` ### 5. Machine Learning with PyTorch For training models, use the experimental PyTorch integration: ```python from cellxgene_census.experimental.ml import experiment_dataloader with cellxgene_census.open_soma() as census: # Create dataloader dataloader = experiment_dataloader( census["census_data"]["homo_sapiens"], measurement_name="RNA", X_name="raw", obs_value_filter="tissue_general == 'liver' and is_primary_data == True", obs_column_names=["cell_type"], batch_size=128, shuffle=True, ) # Training loop for epoch in range(num_epochs): for batch in dataloader: X = batch["X"] # Gene expression tensor labels = batch["obs"]["cell_type"] # Cell type labels # Forward pass outputs = model(X) loss = criterion(outputs, labels) # Backward pass optimizer.zero_grad() loss.backward() optimizer.step() ``` **Train/test splitting:** ```python from cellxgene_census.experimental.ml import ExperimentDataset # Create dataset from experiment dataset = ExperimentDataset( experiment_axis_query, layer_name="raw", obs_column_names=["cell_type"], batch_size=128, ) # Split into train and test train_dataset, test_dataset = dataset.random_split( split=[0.8, 0.2], seed=42 ) ``` ### 6. Integration with Scanpy Seamlessly integrate Census data with scanpy workflows: ```python import scanpy as sc # Load data from Census adata = cellxgene_census.get_anndata( census=census, organism="Homo sapiens", obs_value_filter="cell_type == 'neuron' and tissue_general == 'cortex' and is_primary_data == True", ) # Standard scanpy workflow sc.pp.normalize_total(adata, target_sum=1e4) sc.pp.log1p(adata) sc.pp.highly_variable_genes(adata, n_top_genes=2000) # Dimensionality reduction sc.pp.pca(adata, n_comps=50) sc.pp.neighbors(adata) sc.tl.umap(adata) # Visualization sc.pl.umap(adata, color=["cell_type", "tissue", "disease"]) ``` ### 7. Multi-Dataset Integration Query and integrate multiple datasets: ```python # Strategy 1: Query multiple tissues separately tissues = ["lung", "liver", "kidney"] adatas = [] for tissue in tissues: adata = cellxgene_census.get_anndata( census=census, organism="Homo sapiens", obs_value_filter=f"tissue_general == '{tissue}' and is_primary_data == True", ) adata.obs["tissue"] = tissue adatas.append(adata) # Concatenate combined = adatas[0].concatenate(adatas[1:]) # Strategy 2: Query multiple datasets directly adata = cellxgene_census.get_anndata( census=census, organism="Homo sapiens", obs_value_filter="tissue_general in ['lung', 'liver', 'kidney'] and is_primary_data == True", ) ``` ## Key Concepts and Best Practices ### Always Filter for Primary Data Unless analyzing duplicates, always include `is_primary_data == True` in queries to avoid counting cells multiple times: ```python obs_value_filter="cell_type == 'B cell' and is_primary_data == True" ``` ### Specify Census Version for Reproducibility Always specify the Census version in production analyses: ```python census = cellxgene_census.open_soma(census_version="2023-07-25") ``` ### Estimate Query Size Before Loading For large queries, first check the number of cells to avoid memory issues: ```python # Get cell count metadata = cellxgene_census.get_obs( census, "homo_sapiens", value_filter="tissue_general == 'brain' and is_primary_data == True", column_names=["soma_joinid"] ) n_cells = len(metadata) print(f"Query will return {n_cells:,} cells") # If too large (>100k), use out-of-core processing ``` ### Use tissue_general for Broader Groupings The `tissue_general` field provides coarser categories than `tissue`, useful for cross-tissue analyses: ```python # Broader grouping obs_value_filter="tissue_general == 'immune system'" # Specific tissue obs_value_filter="tissue == 'peripheral blood mononuclear cell'" ``` ### Select Only Needed Columns Minimize data transfer by specifying only required metadata columns: ```python obs_column_names=["cell_type", "tissue_general", "disease"] # Not all columns ``` ### Check Dataset Presence for Gene-Specific Queries When analyzing specific genes, verify which datasets measured them: ```python presence = cellxgene_census.get_presence_matrix( census, "homo_sapiens", var_value_filter="feature_name in ['CD4', 'CD8A']" ) ``` ### Two-Step Workflow: Explore Then Query First explore metadata to understand available data, then query expression: ```python # Step 1: Explore what's available metadata = cellxgene_census.get_obs( census, "homo_sapiens", value_filter="disease == 'COVID-19' and is_primary_data == True", column_names=["cell_type", "tissue_general"] ) print(metadata.value_counts()) # Step 2: Query based on findings adata = cellxgene_census.get_anndata( census=census, organism="Homo sapiens", obs_value_filter="disease == 'COVID-19' and cell_type == 'T cell' and is_primary_data == True", ) ``` ## Available Metadata Fields ### Cell Metadata (obs) Key fields for filtering: - `cell_type`, `cell_type_ontology_term_id` - `tissue`, `tissue_general`, `tissue_ontology_term_id` - `disease`, `disease_ontology_term_id` - `assay`, `assay_ontology_term_id` - `donor_id`, `sex`, `self_reported_ethnicity` - `development_stage`, `development_stage_ontology_term_id` - `dataset_id` - `is_primary_data` (Boolean: True = unique cell) ### Gene Metadata (var) - `feature_id` (Ensembl gene ID, e.g., "ENSG00000161798") - `feature_name` (Gene symbol, e.g., "FOXP2") - `feature_length` (Gene length in base pairs) ## Reference Documentation This skill includes detailed reference documentation: ### references/census_schema.md Comprehensive documentation of: - Census data structure and organization - All available metadata fields - Value filter syntax and operators - SOMA object types - Data inclusion criteria **When to read:** When you need detailed schema information, full list of metadata fields, or complex filter syntax. ### references/common_patterns.md Examples and patterns for: - Exploratory queries (metadata only) - Small-to-medium queries (AnnData) - Large queries (out-of-core processing) - PyTorch integration - Scanpy integration workflows - Multi-dataset integration - Best practices and common pitfalls **When to read:** When implementing specific query patterns, looking for code examples, or troubleshooting common issues. ## Common Use Cases ### Use Case 1: Explore Cell Types in a Tissue ```python with cellxgene_census.open_soma() as census: cells = cellxgene_census.get_obs( census, "homo_sapiens", value_filter="tissue_general == 'lung' and is_primary_data == True", column_names=["cell_type"] ) print(cells["cell_type"].value_counts()) ``` ### Use Case 2: Query Marker Gene Expression ```python with cellxgene_census.open_soma() as census: adata = cellxgene_census.get_anndata( census=census, organism="Homo sapiens", var_value_filter="feature_name in ['CD4', 'CD8A', 'CD19']", obs_value_filter="cell_type in ['T cell', 'B cell'] and is_primary_data == True", ) ``` ### Use Case 3: Train Cell Type Classifier ```python from cellxgene_census.experimental.ml import experiment_dataloader with cellxgene_census.open_soma() as census: dataloader = experiment_dataloader( census["census_data"]["homo_sapiens"], measurement_name="RNA", X_name="raw", obs_value_filter="is_primary_data == True", obs_column_names=["cell_type"], batch_size=128, shuffle=True, ) # Train model for epoch in range(epochs): for batch in dataloader: # Training logic pass ``` ### Use Case 4: Cross-Tissue Analysis ```python with cellxgene_census.open_soma() as census: adata = cellxgene_census.get_anndata( census=census, organism="Homo sapiens", obs_value_filter="cell_type == 'macrophage' and tissue_general in ['lung', 'liver', 'brain'] and is_primary_data == True", ) # Analyze macrophage differences across tissues sc.tl.rank_genes_groups(adata, groupby="tissue_general") ``` ## Troubleshooting ### Query Returns Too Many Cells - Add more specific filters to reduce scope - Use `tissue` instead of `tissue_general` for finer granularity - Filter by specific `dataset_id` if known - Switch to out-of-core processing for large queries ### Memory Errors - Reduce query scope with more restrictive filters - Select fewer genes with `var_value_filter` - Use out-of-core processing with `axis_query()` - Process data in batches ### Duplicate Cells in Results - Always include `is_primary_data == True` in filters - Check if intentionally querying across multiple datasets ### Gene Not Found - Verify gene name spelling (case-sensitive) - Try Ensembl ID with `feature_id` instead of `feature_name` - Check dataset presence matrix to see if gene was measured - Some genes may have been filtered during Census construction ### Version Inconsistencies - Always specify `census_version` explicitly - Use same version across all analyses - Check release notes for version-specific changes