scvi-tools

Compare original and translation side by side

🇺🇸

Original

English
🇨🇳

Translation

Chinese

scvi-tools

scvi-tools

Overview

概述

scvi-tools is a comprehensive Python framework for probabilistic models in single-cell genomics. Built on PyTorch and PyTorch Lightning, it provides deep generative models using variational inference for analyzing diverse single-cell data modalities.
scvi-tools是一个用于单细胞基因组学概率建模的综合性Python框架。它基于PyTorch和PyTorch Lightning构建,提供采用变分推断的深度生成模型,用于分析多种单细胞数据模态。

When to Use This Skill

何时使用该技能

Use this skill when:
  • Analyzing single-cell RNA-seq data (dimensionality reduction, batch correction, integration)
  • Working with single-cell ATAC-seq or chromatin accessibility data
  • Integrating multimodal data (CITE-seq, multiome, paired/unpaired datasets)
  • Analyzing spatial transcriptomics data (deconvolution, spatial mapping)
  • Performing differential expression analysis on single-cell data
  • Conducting cell type annotation or transfer learning tasks
  • Working with specialized single-cell modalities (methylation, cytometry, RNA velocity)
  • Building custom probabilistic models for single-cell analysis
在以下场景中使用该技能:
  • 分析单细胞RNA-seq数据(降维、批次校正、整合)
  • 处理单细胞ATAC-seq或染色质可及性数据
  • 整合多模态数据(CITE-seq、多组学、配对/非配对数据集)
  • 分析空间转录组学数据(反卷积、空间映射)
  • 对单细胞数据进行差异表达分析
  • 执行细胞类型注释或迁移学习任务
  • 处理特殊单细胞模态数据(甲基化、流式细胞术、RNA velocity)
  • 构建用于单细胞分析的自定义概率模型

Core Capabilities

核心功能

scvi-tools provides models organized by data modality:
scvi-tools提供按数据模态分类的模型:

1. Single-Cell RNA-seq Analysis

1. 单细胞RNA-seq分析

Core models for expression analysis, batch correction, and integration. See
references/models-scrna-seq.md
for:
  • scVI: Unsupervised dimensionality reduction and batch correction
  • scANVI: Semi-supervised cell type annotation and integration
  • AUTOZI: Zero-inflation detection and modeling
  • VeloVI: RNA velocity analysis
  • contrastiveVI: Perturbation effect isolation
用于表达分析、批次校正和整合的核心模型。详情见
references/models-scrna-seq.md
  • scVI: 无监督降维和批次校正
  • scANVI: 半监督细胞类型注释与整合
  • AUTOZI: 零膨胀检测与建模
  • VeloVI: RNA velocity分析
  • contrastiveVI: 扰动效应分离

2. Chromatin Accessibility (ATAC-seq)

2. 染色质可及性(ATAC-seq)

Models for analyzing single-cell chromatin data. See
references/models-atac-seq.md
for:
  • PeakVI: Peak-based ATAC-seq analysis and integration
  • PoissonVI: Quantitative fragment count modeling
  • scBasset: Deep learning approach with motif analysis
用于分析单细胞染色质数据的模型。详情见
references/models-atac-seq.md
  • PeakVI: 基于峰的ATAC-seq分析与整合
  • PoissonVI: 定量片段计数建模
  • scBasset: 结合基序分析的深度学习方法

3. Multimodal & Multi-omics Integration

3. 多模态与多组学整合

Joint analysis of multiple data types. See
references/models-multimodal.md
for:
  • totalVI: CITE-seq protein and RNA joint modeling
  • MultiVI: Paired and unpaired multi-omic integration
  • MrVI: Multi-resolution cross-sample analysis
多种数据类型的联合分析。详情见
references/models-multimodal.md
  • totalVI: CITE-seq蛋白与RNA联合建模
  • MultiVI: 配对与非配对多组学整合
  • MrVI: 多分辨率跨样本分析

4. Spatial Transcriptomics

4. 空间转录组学

Spatially-resolved transcriptomics analysis. See
references/models-spatial.md
for:
  • DestVI: Multi-resolution spatial deconvolution
  • Stereoscope: Cell type deconvolution
  • Tangram: Spatial mapping and integration
  • scVIVA: Cell-environment relationship analysis
空间分辨转录组学分析。详情见
references/models-spatial.md
  • DestVI: 多分辨率空间反卷积
  • Stereoscope: 细胞类型反卷积
  • Tangram: 空间映射与整合
  • scVIVA: 细胞-环境关系分析

5. Specialized Modalities

5. 特殊模态

Additional specialized analysis tools. See
references/models-specialized.md
for:
  • MethylVI/MethylANVI: Single-cell methylation analysis
  • CytoVI: Flow/mass cytometry batch correction
  • Solo: Doublet detection
  • CellAssign: Marker-based cell type annotation
额外的专用分析工具。详情见
references/models-specialized.md
  • MethylVI/MethylANVI: 单细胞甲基化分析
  • CytoVI: 流式/质谱细胞术批次校正
  • Solo: 双细胞检测
  • CellAssign: 基于标记物的细胞类型注释

Typical Workflow

典型工作流程

All scvi-tools models follow a consistent API pattern:
python
undefined
所有scvi-tools模型遵循一致的API模式:
python
undefined

1. Load and preprocess data (AnnData format)

1. Load and preprocess data (AnnData format)

import scvi import scanpy as sc
adata = scvi.data.heart_cell_atlas_subsampled() sc.pp.filter_genes(adata, min_counts=3) sc.pp.highly_variable_genes(adata, n_top_genes=1200)
import scvi import scanpy as sc
adata = scvi.data.heart_cell_atlas_subsampled() sc.pp.filter_genes(adata, min_counts=3) sc.pp.highly_variable_genes(adata, n_top_genes=1200)

2. Register data with model (specify layers, covariates)

2. Register data with model (specify layers, covariates)

scvi.model.SCVI.setup_anndata( adata, layer="counts", # Use raw counts, not log-normalized batch_key="batch", categorical_covariate_keys=["donor"], continuous_covariate_keys=["percent_mito"] )
scvi.model.SCVI.setup_anndata( adata, layer="counts", # Use raw counts, not log-normalized batch_key="batch", categorical_covariate_keys=["donor"], continuous_covariate_keys=["percent_mito"] )

3. Create and train model

3. Create and train model

model = scvi.model.SCVI(adata) model.train()
model = scvi.model.SCVI(adata) model.train()

4. Extract latent representations and normalized values

4. Extract latent representations and normalized values

latent = model.get_latent_representation() normalized = model.get_normalized_expression(library_size=1e4)
latent = model.get_latent_representation() normalized = model.get_normalized_expression(library_size=1e4)

5. Store in AnnData for downstream analysis

5. Store in AnnData for downstream analysis

adata.obsm["X_scVI"] = latent adata.layers["scvi_normalized"] = normalized
adata.obsm["X_scVI"] = latent adata.layers["scvi_normalized"] = normalized

6. Downstream analysis with scanpy

6. Downstream analysis with scanpy

sc.pp.neighbors(adata, use_rep="X_scVI") sc.tl.umap(adata) sc.tl.leiden(adata)

**Key Design Principles:**
- **Raw counts required**: Models expect unnormalized count data for optimal performance
- **Unified API**: Consistent interface across all models (setup → train → extract)
- **AnnData-centric**: Seamless integration with the scanpy ecosystem
- **GPU acceleration**: Automatic utilization of available GPUs
- **Batch correction**: Handle technical variation through covariate registration
sc.pp.neighbors(adata, use_rep="X_scVI") sc.tl.umap(adata) sc.tl.leiden(adata)

**核心设计原则:**
- **需要原始计数**:模型为获得最佳性能,要求输入未归一化的计数数据
- **统一API**:所有模型采用一致的接口(设置→训练→提取结果)
- **以AnnData为中心**:与scanpy生态系统无缝集成
- **GPU加速**:自动利用可用的GPU
- **批次校正**:通过协变量注册处理技术变异

Common Analysis Tasks

常见分析任务

Differential Expression

差异表达分析

Probabilistic DE analysis using the learned generative models:
python
de_results = model.differential_expression(
    groupby="cell_type",
    group1="TypeA",
    group2="TypeB",
    mode="change",  # Use composite hypothesis testing
    delta=0.25      # Minimum effect size threshold
)
See
references/differential-expression.md
for detailed methodology and interpretation.
使用学习到的生成模型进行概率性差异表达分析:
python
de_results = model.differential_expression(
    groupby="cell_type",
    group1="TypeA",
    group2="TypeB",
    mode="change",  # Use composite hypothesis testing
    delta=0.25      # Minimum effect size threshold
)
详情见
references/differential-expression.md
了解方法学细节及解读方式。

Model Persistence

模型持久化

Save and load trained models:
python
undefined
保存和加载已训练的模型:
python
undefined

Save model

Save model

model.save("./model_directory", overwrite=True)
model.save("./model_directory", overwrite=True)

Load model

Load model

model = scvi.model.SCVI.load("./model_directory", adata=adata)
undefined
model = scvi.model.SCVI.load("./model_directory", adata=adata)
undefined

Batch Correction and Integration

批次校正与整合

Integrate datasets across batches or studies:
python
undefined
整合不同批次或研究的数据集:
python
undefined

Register batch information

Register batch information

scvi.model.SCVI.setup_anndata(adata, batch_key="study")
scvi.model.SCVI.setup_anndata(adata, batch_key="study")

Model automatically learns batch-corrected representations

Model automatically learns batch-corrected representations

model = scvi.model.SCVI(adata) model.train() latent = model.get_latent_representation() # Batch-corrected
undefined
model = scvi.model.SCVI(adata) model.train() latent = model.get_latent_representation() # Batch-corrected
undefined

Theoretical Foundations

理论基础

scvi-tools is built on:
  • Variational inference: Approximate posterior distributions for scalable Bayesian inference
  • Deep generative models: VAE architectures that learn complex data distributions
  • Amortized inference: Shared neural networks for efficient learning across cells
  • Probabilistic modeling: Principled uncertainty quantification and statistical testing
See
references/theoretical-foundations.md
for detailed background on the mathematical framework.
scvi-tools基于以下理论构建:
  • 变分推断:近似后验分布以实现可扩展的贝叶斯推断
  • 深度生成模型:学习复杂数据分布的VAE架构
  • 摊销推断:共享神经网络以实现跨细胞的高效学习
  • 概率建模:原则性的不确定性量化与统计检验
详情见
references/theoretical-foundations.md
了解数学框架的详细背景。

Additional Resources

额外资源

Installation

安装

bash
uv pip install scvi-tools
bash
uv pip install scvi-tools

For GPU support

For GPU support

uv pip install scvi-tools[cuda]
undefined
uv pip install scvi-tools[cuda]
undefined

Best Practices

最佳实践

  1. Use raw counts: Always provide unnormalized count data to models
  2. Filter genes: Remove low-count genes before analysis (e.g.,
    min_counts=3
    )
  3. Register covariates: Include known technical factors (batch, donor, etc.) in
    setup_anndata
  4. Feature selection: Use highly variable genes for improved performance
  5. Model saving: Always save trained models to avoid retraining
  6. GPU usage: Enable GPU acceleration for large datasets (
    accelerator="gpu"
    )
  7. Scanpy integration: Store outputs in AnnData objects for downstream analysis
  1. 使用原始计数:始终向模型提供未归一化的计数数据
  2. 过滤基因:分析前移除低计数基因(例如
    min_counts=3
  3. 注册协变量:在
    setup_anndata
    中纳入已知的技术因素(批次、供体等)
  4. 特征选择:使用高可变基因以提升性能
  5. 模型保存:始终保存已训练的模型以避免重复训练
  6. GPU使用:对大型数据集启用GPU加速(
    accelerator="gpu"
  7. Scanpy整合:将输出存储在AnnData对象中以便后续分析