alterlab-scvi-tools

Featured

Train deep generative models for single-cell omics with scvi-tools — probabilistic batch correction and integration (scVI), reference-mapping transfer learning (scArches), differential expression with uncertainty, and multimodal models (totalVI for CITE-seq, MultiVI for multiome). Use when correcting batch effects, integrating multimodal data, or doing advanced probabilistic single-cell modeling — for standard analysis pipelines use scanpy. Part of the AlterLab Academic Skills suite.

AI & Automation 66 stars 13 forks Updated 1 weeks ago MIT

Install

View on GitHub

Quality Score: 89/100

Stars 20%
61
Recency 20%
90
Frontmatter 20%
70
Documentation 15%
100
Issue Health 10%
50
License 10%
100
Description 5%
100

Skill Content

# 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-ce...

Details

Author
AlterLab-IEU
Repository
AlterLab-IEU/AlterLab-Academic-Skills
Created
5 months ago
Last Updated
1 weeks ago
Language
Python
License
MIT

Integrates with

Bundled in these plugins

Similar Skills

Semantically similar based on skill content — not just same category

AI & Automation Featured

alterlab-scgpt

Apply the scGPT single-cell foundation model (Cui 2024) to annotate and embed cells — zero-shot and fine-tuned cell-type annotation, gene/cell embeddings, batch integration, and gene-regulatory / perturbation inference from AnnData. Use when annotating cell types with a pretrained foundation model, generating scGPT embeddings, integrating batches with a transformer, or running zero-shot single-cell inference on an h5ad. For probabilistic latent models (scVI/scANVI) prefer alterlab-scvi-tools; for the standard QC→cluster→UMAP→DE pipeline prefer alterlab-scanpy; for the AnnData data structure itself prefer alterlab-anndata; for protein language models prefer alterlab-esm. Part of the AlterLab Academic Skills suite.

66 Updated 1 weeks ago
AlterLab-IEU
AI & Automation Featured

alterlab-scvelo

Run RNA velocity analysis with scVelo on single-cell RNA-seq data — estimate cell-state transitions from spliced/unspliced mRNA dynamics, infer trajectory direction, compute latent time, and identify driver genes. Use when adding directionality to trajectories or studying differentiation dynamics from spliced/unspliced layers (velocyto/STARsolo output); for the general QC, clustering, UMAP, and differential-expression analysis pipeline prefer alterlab-scanpy instead, and for .h5ad data-structure I/O and layer wrangling prefer alterlab-anndata instead. Part of the AlterLab Academic Skills suite.

66 Updated 1 weeks ago
AlterLab-IEU
AI & Automation Featured

alterlab-deeptools

Process and visualize deep-sequencing coverage with the deepTools CLI — convert BAM to bigWig (bamCoverage), build log2 ratio tracks (bamCompare), run QC (multiBamSummary correlation, PCA, plotFingerprint), apply the ATAC-seq Tn5 shift (alignmentSieve --ATACshift), and make TSS/peak heatmaps and profiles (computeMatrix, plotHeatmap, plotProfile). Use for coverage tracks, signal heatmaps/profiles, normalization (RPGC/CPM/RPKM), and effective-genome-size lookups for ChIP-seq, ATAC-seq, MNase-seq, or RNA-seq. NOT for per-read/CIGAR/MAPQ BAM record access — that is pysam. Part of the AlterLab Academic Skills suite.

66 Updated 1 weeks ago
AlterLab-IEU