anndata
DocumentsData structure for annotated matrices in single-cell analysis; use when reading/writing .h5ad (or zarr) and exchanging data with the scverse ecosystem.
How to use this skill
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When to Use
Use AnnData when you need to:
- Load, inspect, or export annotated single-cell datasets stored as
.h5ad(orzarr) for downstream tools. - Keep a matrix (cells × features) tightly coupled with observation/feature metadata (e.g., cell types, batches, gene annotations).
- Work efficiently with large, sparse count matrices (e.g., scRNA-seq) and avoid loading everything into memory (backed mode).
- Combine multiple experiments/batches/modalities into a unified object while tracking provenance.
- Subset/filter/transform data while preserving alignment between the matrix and metadata.
Key Features
- Unified container:
X(data matrix) plus aligned annotations:obs,var,uns, and multi-dimensional slots (obsm,varm,obsp,varp), pluslayersand optionalraw. - Interoperable I/O: Native
.h5adandzarr, plus common genomics formats (e.g., 10x, loom, mtx, csv). - Scalable workflows: Sparse matrices and backed mode (
backed="r") for large datasets. - Safe subsetting: Slicing preserves alignment across matrix and annotations; supports views vs copies.
- Concatenation utilities:
ad.concat(...)with join/merge strategies and batch labeling; experimental lazy collections.
Reference notes: the original material mentions additional guides under
references/(e.g.,references/data_structure.md,references/io_operations.md,references/concatenation.md,references/manipulation.md,references/best_practices.md) for deeper explanations of each topic.
Dependencies
anndata(latest compatible with your environment; install via pip/uv)numpypandasscipy(recommended for sparse matrices)- Optional ecosystem tools (only if needed):
scanpymuontorch(for deep learning) andanndataexperimental loader utilities
Example Usage
A complete runnable example that creates an AnnData object, writes/reads .h5ad, subsets, concatenates batches, and demonstrates backed mode.
import numpy as np
import pandas as pd
import anndata as ad
from scipy.sparse import csr_matrix
# ----------------------------
# 1) Create an AnnData object
# ----------------------------
rng = np.random.default_rng(0)
n_cells, n_genes = 100, 500
X = rng.poisson(1.0, size=(n_cells, n_genes)).astype(np.float32)
obs = pd.DataFrame(
{
"cell_type": (["T cell", "B cell"] * (n_cells // 2)),
"sample": (["A", "B"] * (n_cells // 2)),
"quality_score": rng.random(n_cells),
},
index=[f"cell_{i}" for i in range(n_cells)],
)
var = pd.DataFrame(
{"gene_name": [f"Gene_{j}" for j in range(n_genes)]},
index=[f"ENSG{j:05d}" for j in range(n_genes)],
)
adata = ad.AnnData(X=X, obs=obs, var=var)
# Use sparse storage for typical count-like matrices
adata.X = csr_matrix(adata.X)
# Convert string columns to categoricals to reduce memory and speed up ops
adata.strings_to_categoricals()
print(f"Created: {adata.n_obs} obs × {adata.n_vars} vars")
# ----------------------------
# 2) Write and read .h5ad
# ----------------------------
adata.write_h5ad("example.h5ad", compression="gzip")
adata2 = ad.read_h5ad("example.h5ad")
print(f"Reloaded: {adata2.n_obs} obs × {adata2.n_vars} vars")
# ----------------------------
# 3) Subset (keeps alignment)
# ----------------------------
t_cells = adata2[adata2.obs["cell_type"] == "T cell", :]
high_quality = adata2[adata2.obs["quality_score"] > 0.8, :]
print(f"T cells: {t_cells.n_obs}")
print(f"High quality: {high_quality.n_obs}")
# ----------------------------
# 4) Concatenate batches
# ----------------------------
adata_a = adata2[adata2.obs["sample"] == "A", :].copy()
adata_b = adata2[adata2.obs["sample"] == "B", :].copy()
combined = ad.concat(
[adata_a, adata_b],
axis=0, # concatenate observations (cells)
join="inner", # keep shared variables
label="batch", # add a column in .obs
keys=["A", "B"], # batch labels
)
print(combined.obs["batch"].value_counts().to_dict())
# ----------------------------
# 5) Backed mode for large files
# ----------------------------
adata_backed = ad.read_h5ad("example.h5ad", backed="r")
# Slicing in backed mode is metadata-friendly; load to memory when needed:
subset_mem = adata_backed[:10, :50].to_memory()
print(f"Backed subset loaded: {subset_mem.shape}")
Implementation Details
Data model (core slots)
X: primary data matrix (densenumpy.ndarrayor sparsescipy.sparse), shape(n_obs, n_vars).obs: per-observation metadata (pandas.DataFrame), indexed byobs_names(e.g., cell IDs).var: per-variable metadata (pandas.DataFrame), indexed byvar_names(e.g., gene IDs).layers: named alternative matrices aligned toX(e.g.,"counts","log1p").obsm/varm: multi-dimensional embeddings aligned to obs/var (e.g., PCA, UMAP coordinates).obsp/varp: pairwise graphs/matrices (e.g., kNN graph inobsp["connectivities"]).uns: unstructured metadata (dict-like), often used for parameters and plotting configs.raw(optional): snapshot of unfiltered/untransformed data for reproducibility.
Views vs copies
- Slicing like
adata_subset = adata[mask, :]typically returns a view (lightweight reference). - Use
.copy()when you need an independent object (e.g., before in-place modifications).
Backed mode (large datasets)
ad.read_h5ad(path, backed="r")keeps the matrix on disk and loads data lazily.- Convert a slice to memory with
.to_memory()when you need in-memory computation. - Backed mode is best for filtering by metadata, chunked processing, and avoiding OOM.
Concatenation behavior
ad.concat([...], axis=0)stacks observations;axis=1stacks variables.join="inner"keeps intersection of variables;join="outer"unions variables (may introduce missing values).label+keysrecords dataset/batch provenance in.obs[label].- Merge strategies control how conflicting
.unsand annotation columns are handled (choose based on your data governance needs).
Practical performance parameters
- Prefer sparse matrices (
csr_matrix) for count-like data. - Convert repeated strings to categoricals (
adata.strings_to_categoricals()). - Use compression when writing
.h5ad(e.g.,compression="gzip") to reduce storage; considerzarrfor chunked/cloud-friendly access.