scrna-seq-pipeline

name	scrna-seq-pipeline
description	Scanpy-based single-cell RNA-seq analysis pipeline covering loading (10X, h5ad), QC, normalization, HVG selection, PCA/UMAP, Leiden clustering, differential expression, and batch correction (Harmony, scVI). Use when the user mentions single-cell, scRNA-seq, Scanpy, AnnData, UMAP, clustering, 10X, h5ad, leiden, highly variable genes, Harmony, scVI, cluster cells, find marker genes, filter low-quality cells, gene expression matrix, doublet removal, normalize counts, dimensionality reduction, cell clustering, QC single-cell, filtered_feature_bc_matrix, cellranger output, 10X h5, scrublet, cell ranger, count matrix, find cell types, batch effect, integration, neighborhood graph, or differential expression genes.
usage	Invoke when processing scRNA-seq data with Scanpy, including QC, normalization, clustering, DE, or batch correction.
version	1.0.0
validated_against	{"date":"2025-01-15T00:00:00.000Z","packages":{"scanpy":"1.10","anndata":"0.10","scvi-tools":"1.1"}}
tags	["skill","category:pipeline","single-cell","scanpy","scrna-seq","hcls"]

scRNA-seq Pipeline (Scanpy)

Overview

This skill produces a reproducible scRNA-seq analysis in Python using Scanpy and AnnData. It covers the standard workflow: load counts → QC filter → normalize/log → HVG → scale/PCA → neighbors/UMAP → Leiden → differential expression, plus batch correction with Harmony or scVI. Default parameters follow the Scanpy PBMC3k tutorial conventions and are safe starting points for most 10X Genomics datasets.

Output is a single .h5ad file with all intermediate embeddings, cluster labels, and DE results stored on the AnnData object.

Usage

Install dependencies:

pip install "scanpy>=1.10" anndata leidenalg python-igraph harmonypy scvi-tools

Run the pipeline end-to-end:

import scanpy as sc
import scanpy.external as sce

sc.settings.verbosity = 2
sc.settings.set_figure_params(dpi=100, facecolor="white")

# 1. Load
adata = sc.read_10x_h5("filtered_feature_bc_matrix.h5")
# Alternatives:
# adata = sc.read_10x_mtx("filtered_feature_bc_matrix/", var_names="gene_symbols", cache=True)
# adata = sc.read_h5ad("input.h5ad")
adata.var_names_make_unique()

# 2. QC
adata.var["mt"] = adata.var_names.str.startswith("MT-")
sc.pp.calculate_qc_metrics(adata, qc_vars=["mt"], percent_top=None, log1p=False, inplace=True)
sc.pp.filter_cells(adata, min_genes=200)
sc.pp.filter_genes(adata, min_cells=3)
adata = adata[adata.obs.n_genes_by_counts < 5000, :]
adata = adata[adata.obs.pct_counts_mt < 20, :].copy()

# 3. Normalize + HVG
sc.pp.normalize_total(adata, target_sum=1e4)
sc.pp.log1p(adata)
adata.raw = adata  # freeze log-normalized full gene set BEFORE HVG subset
sc.pp.highly_variable_genes(adata, n_top_genes=2000, flavor="seurat")
adata = adata[:, adata.var.highly_variable].copy()

# 4. Scale + PCA + neighbors + UMAP + Leiden
sc.pp.scale(adata, max_value=10)
sc.tl.pca(adata, n_comps=50, svd_solver="arpack")
sc.pp.neighbors(adata, n_neighbors=15, n_pcs=30)
sc.tl.umap(adata)
sc.tl.leiden(adata, resolution=0.5)

# 5. Differential expression per cluster
sc.tl.rank_genes_groups(adata, groupby="leiden", method="wilcoxon")

# 6. Save
adata.write("result.h5ad", compression="gzip")

Batch correction — Harmony

# Assumes adata.obs["batch"] exists and PCA is already computed.
sce.pp.harmony_integrate(adata, key="batch")  # writes adata.obsm["X_pca_harmony"]
sc.pp.neighbors(adata, n_neighbors=15, n_pcs=30, use_rep="X_pca_harmony")
sc.tl.umap(adata)
sc.tl.leiden(adata, resolution=0.5)

Batch correction — scVI

scVI requires raw counts. Run it before normalization, or keep a raw-count layer.

import scvi

# adata_raw holds unnormalized integer counts; adata.obs["batch"] is the batch key.
scvi.model.SCVI.setup_anndata(adata_raw, batch_key="batch")
model = scvi.model.SCVI(adata_raw, n_latent=30)
model.train(max_epochs=400, early_stopping=True)
adata.obsm["X_scVI"] = model.get_latent_representation()

sc.pp.neighbors(adata, n_neighbors=15, use_rep="X_scVI")
sc.tl.umap(adata)
sc.tl.leiden(adata, resolution=0.5)

Response Format

• Lead with the command or code the user needs — explain after
• Structure as: confirm inputs → working code → key parameters explained → gotchas
• One complete working example per task; do not show every alternative
• Keep code comments minimal and functional (what, not why-it-exists)
• Target: 50-100 lines of code with brief surrounding explanation

Core Concepts

• AnnData layout. adata.X is the current expression matrix (cells × genes). adata.obs holds per-cell metadata (QC metrics, cluster labels, batch). adata.var holds per-gene metadata (HVG flags, mt). Embeddings live in adata.obsm (X_pca, X_umap, X_scVI). Neighbor graph and DE results live in adata.uns.
• .raw snapshot. adata.raw = adata stores the full log-normalized matrix before HVG subsetting. Downstream plotting functions (sc.pl.umap(..., color="GENE"), sc.pl.rank_genes_groups) read from .raw so you can visualize any gene even after restricting adata to HVGs.
• QC thresholds are dataset-dependent. n_genes ∈ [200, 5000] and pct_mt < 20 are reasonable defaults for human 10X PBMC-like data. Inspect distributions (sc.pl.violin) before committing. Use MT- for human and mt- for mouse.
• HVG flavor matters. Use flavor="seurat" on log-normalized data (default). Use flavor="seurat_v3" on raw counts — it expects integer counts and will error or mislead on log data.
• Neighbors parameters. n_neighbors controls local/global structure (10–50; larger = smoother UMAP). n_pcs should capture the elbow in sc.pl.pca_variance_ratio (typically 20–50). Leiden resolution controls cluster granularity (0.2–1.5; higher = more clusters).
• Batch correction choice. Harmony is fast, operates on PCA, and works well for mild-to-moderate batch effects. scVI is a deep generative model, needs raw counts and GPU for speed, and handles stronger technical variation and multi-modal designs.

Quick Reference

Loading

Input	Call
10X HDF5	sc.read_10x_h5("filtered_feature_bc_matrix.h5")
10X MTX dir	sc.read_10x_mtx("path/", var_names="gene_symbols", cache=True)
Existing AnnData	sc.read_h5ad("input.h5ad")
Always after load	adata.var_names_make_unique()

Key parameter ranges

Parameter	Default	Typical range	Notes
filter_cells(min_genes=)	200	100–500	Drop empty/low-quality droplets
filter_genes(min_cells=)	3	3–10	Drop rarely-expressed genes
n_genes_by_counts <	5000	2500–8000	Upper bound flags doublets
pct_counts_mt <	20	5–25	Human tissue dependent
normalize_total(target_sum=)	1e4	1e4	CP10k; standard
n_top_genes (HVG)	2000	1000–5000	More HVGs → more signal + noise
scale(max_value=)	10	10	Clip extreme z-scores
pca(n_comps=)	50	30–100	Pick elbow for downstream n_pcs
neighbors(n_neighbors=)	15	10–50	Larger → smoother manifold
neighbors(n_pcs=)	30	20–50	≤ n_comps
leiden(resolution=)	0.5	0.2–1.5	Higher → more clusters

DE & inspection

sc.tl.rank_genes_groups(adata, groupby="leiden", method="wilcoxon")
sc.pl.rank_genes_groups(adata, n_genes=25, sharey=False)

# Top-N markers per cluster as a DataFrame
import pandas as pd
result = adata.uns["rank_genes_groups"]
groups = result["names"].dtype.names
markers = pd.DataFrame({g: result["names"][g][:20] for g in groups})

Saving / loading

adata.write("result.h5ad", compression="gzip")
adata = sc.read_h5ad("result.h5ad")

Common Mistakes

• Wrong: Subsetting to HVGs before saving adata.raw = adata Right: Always set .raw on the log-normalized full matrix before adata = adata[:, adata.var.highly_variable].copy() Why: Without .raw, you lose the ability to plot or score non-HVG genes in downstream analysis

• Wrong: Using flavor="seurat_v3" on log-normalized data Right: Match HVG flavor to data state: seurat_v3 requires raw integer counts; seurat (default) requires log-normalized data Why: Wrong flavor produces nonsense HVG rankings or errors, corrupting all downstream steps

• Wrong: Skipping adata.var_names_make_unique() after loading 10X data Right: Call adata.var_names_make_unique() immediately after loading Why: Duplicated gene symbols cause silent misbehavior in indexing, HVG selection, and DE analysis

• Wrong: Running scVI on normalized/log-transformed data Right: Feed scVI the raw-count AnnData and set batch_key via setup_anndata Why: scVI models counts directly; normalized input violates its distributional assumptions and produces incorrect latent spaces

• Wrong: Using MT- prefix for mouse mitochondrial genes (or mt- for human) Right: Use MT- for human genes and mt- for mouse genes Why: Wrong prefix makes pct_counts_mt always zero, rendering the QC filter a no-op

• Wrong: Boolean-slicing AnnData without calling .copy() Right: Always use .copy() after filtering: adata = adata[mask, :].copy() Why: Without .copy(), the result is a view; subsequent in-place operations will warn or fail

References

• Scanpy: Wolf et al. Genome Biol 2018, https://doi.org/10.1186/s13059-017-1382-0
• Scanpy tutorials: https://scanpy.readthedocs.io/en/stable/tutorials.html
• scVI: Gayoso et al. Nat Biotechnol 2022, https://doi.org/10.1038/s41587-021-01206-w
• Harmony: Korsunsky et al. Nat Methods 2019, https://doi.org/10.1038/s41592-019-0619-0