Data structure for annotated matrices in single-cell analysis. Use when working with .h5ad files or integrating with the scverse ecosystem. This is the data format skill—for analysis workflows use scanpy; for probabilistic models use scvi-tools; for population-scale queries use cellxgene-census.
Data structure for annotated matrices in single-cell analysis. Use when working with .h5ad files or integrating with the scverse ecosystem. This is the data format skill—for analysis workflows use scanpy; for probabilistic models use scvi-tools; for population-scale queries use cellxgene-census.
license
BSD-3-Clause license
metadata
{"skill-author":"K-Dense Inc."}
verified
false
lastVerifiedAt
"2026-02-19T05:29:09.098Z"
source
builtin
trust_score
100
provenance_sha
4d3fc48be3fbe557
AnnData
Overview
AnnData is a Python package for handling annotated data matrices, storing experimental measurements (X) alongside observation metadata (obs), variable metadata (var), and multi-dimensional annotations (obsm, varm, obsp, varp, uns). Originally designed for single-cell genomics through Scanpy, it now serves as a general-purpose framework for any annotated data requiring efficient storage, manipulation, and analysis.
When to Use This Skill
Use this skill when:
Creating, reading, or writing AnnData objects
Working with h5ad, zarr, or other genomics data formats
Performing single-cell RNA-seq analysis
Managing large datasets with sparse matrices or backed mode
Concatenating multiple datasets or experimental batches
Subsetting, filtering, or transforming annotated data
Integrating with scanpy, scvi-tools, or other scverse ecosystem tools
# Use sparse matrices for sparse datafrom scipy.sparse import csr_matrix
adata.X = csr_matrix(adata.X)
# Convert strings to categoricals
adata.strings_to_categoricals()
# Use backed mode for large files
adata = ad.read_h5ad('large.h5ad', backed='r')
# Store raw before filtering
adata.raw = adata.copy()
adata = adata[:, adata.var['highly_variable']]
Integration with Scverse Ecosystem
AnnData serves as the foundational data structure for the scverse ecosystem:
import muon as mu
# Combine RNA and protein data
mdata = mu.MuData({'rna': adata_rna, 'protein': adata_protein})
PyTorch integration
from anndata.experimental import AnnLoader
# Create DataLoader for deep learning
dataloader = AnnLoader(adata, batch_size=128, shuffle=True)
for batch in dataloader:
X = batch.X
# Train model
Common Workflows
Single-cell RNA-seq analysis
import anndata as ad
import scanpy as sc
# 1. Load data
adata = ad.read_10x_h5('filtered_feature_bc_matrix.h5')
# 2. Quality control
adata.obs['n_genes'] = (adata.X > 0).sum(axis=1)
adata.obs['n_counts'] = adata.X.sum(axis=1)
adata = adata[adata.obs['n_genes'] > 200]
adata = adata[adata.obs['n_counts'] < 50000]
# 3. Store raw
adata.raw = adata.copy()
# 4. Normalize and filter
sc.pp.normalize_total(adata, target_sum=1e4)
sc.pp.log1p(adata)
sc.pp.highly_variable_genes(adata, n_top_genes=2000)
adata = adata[:, adata.var['highly_variable']]
# 5. Save processed data
adata.write_h5ad('processed.h5ad')
# Open in backed mode
adata = ad.read_h5ad('100GB_dataset.h5ad', backed='r')
# Filter based on metadata (no data loading)
high_quality = adata[adata.obs['quality_score'] > 0.8]
# Load filtered subset
adata_subset = high_quality.to_memory()
# Process subset
process(adata_subset)
# Or process in chunks
chunk_size = 1000for i inrange(0, adata.n_obs, chunk_size):
chunk = adata[i:i+chunk_size, :].to_memory()
process(chunk)
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