Transform lengthy academic papers into concise, structured 250-word abstracts.
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。
Data structure for annotated matrices in single-cell analysis; use when reading/writing .h5ad (or zarr) and exchanging data with the scverse ecosystem.
インストールする前に、エージェントに与えられる指示の中身を確認できます。
Use AnnData when you need to:
.h5ad (or zarr) for downstream tools.X (data matrix) plus aligned annotations: obs, var, uns, and multi-dimensional slots (obsm, varm, obsp, varp), plus layers and optional raw..h5ad and zarr, plus common genomics formats (e.g., 10x, loom, mtx, csv).backed="r") for large datasets.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.
anndata (latest compatible with your environment; install via pip/uv)numpypandasscipy (recommended for sparse matrices)scanpymuontorch (for deep learning) and anndata experimental loader utilitiesA 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}")
X: primary data matrix (dense numpy.ndarray or sparse scipy.sparse), shape (n_obs, n_vars).obs: per-observation metadata (pandas.DataFrame), indexed by obs_names (e.g., cell IDs).var: per-variable metadata (pandas.DataFrame), indexed by var_names (e.g., gene IDs).layers: named alternative matrices aligned to X (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 in obsp["connectivities"]).uns: unstructured metadata (dict-like), often used for parameters and plotting configs.raw (optional): snapshot of unfiltered/untransformed data for reproducibility.adata_subset = adata[mask, :] typically returns a view (lightweight reference)..copy() when you need an independent object (e.g., before in-place modifications).ad.read_h5ad(path, backed="r") keeps the matrix on disk and loads data lazily..to_memory() when you need in-memory computation.ad.concat([...], axis=0) stacks observations; axis=1 stacks variables.join="inner" keeps intersection of variables; join="outer" unions variables (may introduce missing values).label + keys records dataset/batch provenance in .obs[label]..uns and annotation columns are handled (choose based on your data governance needs).csr_matrix) for count-like data.adata.strings_to_categoricals())..h5ad (e.g., compression="gzip") to reduce storage; consider zarr for chunked/cloud-friendly access.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
Transform lengthy academic papers into concise, structured 250-word abstracts.
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。
Precision editing tool that reduces abstract word count through intelligent compression techniques, maintaining scientific rigor while meeting strict journal and conference requirements.
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。
Refines long medical academic texts into SCI-style unstructured Chinese and English abstracts; use when you need to condense drafts/reports/summaries into bilingual abstracts and generate Summary_Report.md.
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。
Generates submission-ready Elsevier/SCI Highlights from manuscript text or extracted PDF/DOCX/TXT content. Use when a user needs 3-5 concise, evidence-grounded highlight bullets for a research paper, review, meta-analysis, case report, or bioinformatics manuscript.
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。
Generates complete FAERS pharmacovigilance study designs for multi-drug or class-level safety comparison inside one predefined SOC or AE family using active comparators, disproportionality analysis, subgroup characterization, and reviewer-facing evidence control.
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。
Analyze data with `adme-property-predictor` using a reproducible workflow, explicit validation, and structured outputs for review-ready interpretation.
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。