scvi-tools-single-cell
De la autor
Deep generative models for single-cell omics: probabilistic batch correction (scVI), semi-supervised annotation (scANVI), CITE-seq RNA+protein (totalVI), transfer learning (scARCHES), and DE with uncertainty. Unified setup→train→extract API on AnnData. Use harmony-batch-correction for fast linear correction without deep learning; muon for multi-modal MuData workflows.
Instalare
npx skills add jaechang-hits/SciAgent-Skills --skill scvi-tools-single-cell -a claude-code
Se instalează în .claude/skills/scvi-tools-single-cell/ · Fiecare comandă descarcă skill-ul direct de pe GitHub cu utilitarul open source skills.
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Skill-uri similare
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- scvi-toolsanthropics/knowledge-work-pluginsDeep learning for single-cell analysis using scvi-tools. This skill should be used when users need (1) data integration and batch correction with scVI/scANVI, (2) ATAC-seq analysis with PeakVI, (3) CITE-seq multi-modal analysis with totalVI, (4) multiome RNA+ATAC analysis with MultiVI, (5) spatial transcriptomics deconvolution with DestVI, (6) label transfer and reference mapping with scANVI/scArches, (7) RNA velocity with veloVI, or (8) any deep learning-based single-cell method. Triggers include mentions of scVI, scANVI, totalVI, PeakVI, MultiVI, DestVI, veloVI, sysVI, scArches, variational autoencoder, VAE, batch correction, data integration, multi-modal, CITE-seq, multiome, reference mapping, latent space.OficialAltele★ 31.9K
- scgptaipoch/open-scienceEmbed and annotate single-cell expression data with scGPT, a foundation model for single-cell biology. Use this skill when: (1) Producing cell embeddings from an AnnData for clustering/integration, (2) Zero-shot or fine-tuned cell-type annotation, (3) Gene-level representation for perturbation/GRN tasks. For probabilistic single-cell models (scVI etc.), use the scvi-tools library.Știință★ 5.4K
- multimodal-omics-integrationjaechang-hits/SciAgent-SkillsMultimodal and multi-section integration for spatial and single-cell omics: totalVI joint RNA + protein (Visium CytAssist Gene and Protein, CITE-seq), MultiVI joint RNA + ATAC (10x Multiome, spatial ATAC-RNA), BBKNN integration of several tissue sections, scanpy ingest label transfer between sections, and gene signature scores mapped on tissue. Outputs joint latent spaces, denoised protein maps, integrated clusters, transferred labels. For dissociated CITE-seq and scVI/scANVI use scvi-tools-single-cell; for MOFA+ factor analysis use mofaplus-multi-omics or muon-multiomics-singlecell; for Harmony use harmony-batch-correction.Știință★ 382
- muon-multiomics-singlecelljaechang-hits/SciAgent-SkillsMulti-modal single-cell analysis with muon/MuData. Joint RNA+ATAC (10x Multiome), CITE-seq (RNA+protein), other multi-omics. MuData holds per-modality AnnData with shared obs. WNN joint embedding, per-modality preprocessing, MOFA factor analysis. Use scanpy-scrna-seq for single-modality RNA; use muon when combining 2+ omics from the same cells.Știință★ 382
- scanpyK-Dense-AI/scientific-agent-skillsPerforms Scanpy single-cell RNA-seq QC, normalization, HVG selection, PCA/UMAP/t-SNE, clustering, exploratory marker ranking, pseudobulk preparation, visualization, and Seurat or SingleCellExperiment RDS conversion to h5ad. Applies to established exploratory scRNA-seq workflows with explicit count and expression provenance; complementary skills cover scvi-tools models and AnnData format details.Marketing★ 54.1K
- anndataK-Dense-AI/scientific-agent-skillsHandles annotated matrices in single-cell analysis, .h5ad and Zarr files, and integration with the scverse ecosystem. This is the data format skill—for analysis workflows use scanpy; for probabilistic models use scvi-tools; for population-scale queries use cellxgene-census.Altele★ 54.1K
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