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Agent Skill · 前端设计

scvi-tools(scvi-tools 单细胞分析)

用于辅助文档、README、Markdown、说明文和内容稿件的整理与改写。它适合让 Agent 提炼结构、补齐章节、统一术语、检查链接或把零散材料整理成可读文档。使用时应保留项目已有事实、命令和路径,不要把未确认的信息写成确定结论;涉及对外文案时,还需要控制语气,避免过度营销或夸大能力。

scvi-tools 是前端设计类 Agent Skill,可用宿主为 Codex、Claude、Cursor、Gemini CLI,通过GitHub 仓库获取,权限为需要联网;许可证为 MIT,第三方扫描已通过,按安装量在前端设计类的 10,216 个 Skill 里排第 7,232。

总安装 399周安装 16GitHub Stars 3下载 129核验 2026-05-01

安装说明

本站只整理中文说明,不托管安装包,也不代用户安装。
GitHub
许可证
MIT

安装方式

通过对话安装

复制提示词发给支持本地命令或 Skills 的 AI 助手,先确认命令和权限,再让它执行。

请帮我安装这个 Agent Skill:scvi-tools(scvi-tools 单细胞分析)
来源仓库:https://github.com/drshailesh88/integrated_content_os
仓库路径:skills/scvi-tools
安装命令:
npx skills add https://github.com/drshailesh88/integrated_content_os --skill scvi-tools
安装前请先检查当前环境是否支持对应 CLI,并向我确认将要执行的命令、安装目录、联网范围和文件读写权限;确认后再执行。

命令行安装

复制命令到本机终端执行。不同来源提供的安装方式可能略有差异;本站展示可直接复制的安装命令,安装前请核对来源页面。

skills.shnpx skills
npx skills add https://github.com/drshailesh88/integrated_content_os --skill scvi-tools

这个 Skill 是做什么的

前端设计类 Skill 关注页面结构、视觉规范和组件写法,输出通常是可运行的界面代码。

用于单细胞多组学数据的深度生成建模。实现批次效应去除与跨样本整合分析。scvi-tools 属于前端设计类 Skill,可作为该场景下的辅助能力补充。支持CITE-seq与空间转录组数据联合建模。安装需指定仓库路径,使用npx命令添加技能。显存不足时可降低批量大小分批处理。

适用宿主包括 Codex、Claude、Cursor、Gemini CLI,接入前应确认版本、权限和运行环境要求。

来源仓库内路径:skills/scvi-tools

上手步骤

4 步
  1. 1

    确认自己的宿主工具

    公开资料标注支持 Codex、Claude、Cursor、Gemini CLI;先确认自己用的是其中之一,再按对应工具的 Skills 目录放置。

  2. 2

    拿到安装命令

    可以直接复制的命令是 npx skills add https://github.com/drshailesh88/integrated_content_os --skill scv…;命令里的占位符换成自己的路径或密钥再执行。

  3. 3

    安装后重启宿主

    命令执行完要完全退出宿主工具再打开,让新装的 Skill 被重新扫描到,否则列表里可能看不到。

  4. 4

    按最小权限试用

    它需要需要联网,先在测试目录或测试账号里跑,确认没问题再放到正式项目。

常见问题

6 条

scvi-tools 怎么安装?

在终端执行 npx skills add https://github.com/drshailesh88/integrated_content_os --skill scvi-tools。装完完全退出宿主工具再打开,让它重新扫描本地 Skill。

scvi-tools 支持哪些 AI 工具?

公开资料标注支持 Codex、Claude、Cursor、Gemini CLI。其他工具只要能读取本地 Skill 目录,一般也能手动放进去,但要自己确认触发方式是否一致。

scvi-tools 需要什么权限?

权限级别是需要联网。该 Skill 可能需要联网访问来源站点、仓库或外部 API;具体网络访问范围需要结合源码和 README 复核。

scvi-tools 是免费的吗?

来源标注的许可证是 MIT。本站不代收任何费用,也不托管安装包;能否商用、要不要署名,以许可证原文为准。

scvi-tools 用的人多吗?

公开数据是累计安装 399 次,近一周安装 16 次,下载 129 次,GitHub 3 星。这些数字来自第三方目录统计,只能当作热度参考,不代表质量或安全性。

scvi-tools 安全吗?

第三方扫描结果为通过,但这只覆盖已知的静态检查项,不能替代自己读一遍源码和安装命令。

值得选的地方和要先想清楚的地方

值得选的地方

  • 同时适配 4 种工具,换客户端不用重新找替代品。
  • 3 个目录同时收录,说明这个 Skill 流传比较广。
  • 许可证明确为 MIT,商用和分发边界好判断。
  • 第三方扫描已通过,常见的高风险行为没有命中。

先想清楚的地方

  • 第三方目录整理,版本更新和行为细节以来源仓库为准。

适不适合你

更适合

  • 已经在用 Codex,想直接扩展它能力的人。
  • 需要处理前端设计类任务、又不想每次都手写提示词的人。
  • 需要许可证清楚、并且有第三方扫描结果的团队项目。

不太适合

  • 需要厂商级技术支持和 SLA 的生产系统。

前端设计类 Skill 对比

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8,823,360126,072只读MIT通过
vercel-composition-patterns

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vercel-react-native-skills

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2,468,66425,878只读MIT通过
adapt

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2,027,04023,125操作浏览器未明确通过
bolder

bolder 分析 · Codex、Claude

2,004,28823,130只读未明确通过
scvi-tools

scvi-tools 单细胞分析 · 本页

3993需要联网MIT通过

按安装量取同分类前几名;数字来自第三方目录统计,只作热度参考,不代表质量结论。

SKILL.md 原文

scvi-tools

Overview

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.

When to Use This Skill

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

Core Capabilities

scvi-tools provides models organized by data modality:

1. Single-Cell RNA-seq Analysis

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

2. Chromatin Accessibility (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

3. Multimodal & Multi-omics Integration

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

4. Spatial Transcriptomics

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

5. Specialized Modalities

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

Typical Workflow

All scvi-tools models follow a consistent API pattern:

# 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)

# 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"]
)

# 3. Create and train model
model = scvi.model.SCVI(adata)
model.train()

# 4. Extract latent representations and normalized values
latent = model.get_latent_representation()
normalized = model.get_normalized_expression(library_size=1e4)

# 5. Store in AnnData for downstream analysis
adata.obsm["X_scVI"] = latent
adata.layers["scvi_normalized"] = normalized

# 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

Common Analysis Tasks

Differential Expression

Probabilistic DE analysis using the learned generative models:

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.

Model Persistence

Save and load trained models:

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

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

Batch Correction and Integration

Integrate datasets across batches or studies:

# Register batch information
scvi.model.SCVI.setup_anndata(adata, batch_key="study")

# Model automatically learns batch-corrected representations
model = scvi.model.SCVI(adata)
model.train()
latent = model.get_latent_representation()  # Batch-corrected

Theoretical Foundations

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.

Additional Resources

Installation

uv pip install scvi-tools
# For GPU support
uv pip install scvi-tools[cuda]

Best Practices

  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

平台分布

Claude Code

27.14%
按下载量换算35

OpenCode

21.64%
按下载量换算28

Antigravity

17.35%
按下载量换算22

Gemini CLI

14.71%
按下载量换算19

windsurf

7.89%
按下载量换算10

Codex

3.95%
按下载量换算5

安全审计

Gen Agent Trust Hub

通过

Socket

通过

Snyk

通过

权限和风险

需要联网

该 Skill 可能需要联网访问来源站点、仓库或外部 API;具体网络访问范围需要结合源码和 README 复核。

安装前确认

本站仅展示第三方公开信息,不托管安装包,不提供自动安装或运行环境。安装前应自行审查源码、依赖和命令行为。

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