scanpy-scrna-seq
From the author
scRNA-seq with Scanpy: QC, normalization, HVG selection, PCA, neighborhood graph, UMAP/t-SNE, Leiden clustering, markers, cell annotation, trajectory inference. Standard scRNA-seq exploration.
Install
npx skills add jaechang-hits/SciAgent-Skills --skill scanpy-scrna-seq -a claude-code
Installs to .claude/skills/scanpy-scrna-seq/ · Each command fetches the skill straight from GitHub with the open skills CLI.
Download .zip
Byte-identical to the scanned commit, with the repository’s licence and a SOURCE.txt.
Want your agent to suggest skills while you type? See how to use skills from your IDE.
Safety checks on SKILL.md
No warnings.
Why 86
Security100
Provenance71
Maintenance100
Licence100
Adoption43
aiqbench computes the trust score from public signals. It is not a security audit, so read a skill before you install it.
Similar skills
Closest to this one by what they do and when they are used.
- 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
- scveloK-Dense-AI/scientific-agent-skillsPerforms RNA velocity analysis with scVelo from spliced and unspliced single-cell RNA counts. Fits deterministic or dynamical models, examines gene phase portraits, builds velocity graphs, estimates relative latent time, and ranks velocity-associated genes. Use for directional trajectory hypotheses and kinetic-model diagnostics alongside Scanpy; velocity alone does not establish cell fate or causal drivers.Other★ 54.1K
- spatial-transcriptomics-analysis-squidpyjaechang-hits/SciAgent-SkillsSquidpy spatial statistics on annotated spatial transcriptomics: build the spatial graph (Visium grid, kNN, radius, Delaunay), neighbourhood enrichment z-scores, distance-resolved co-occurrence, interaction matrix and centrality scores, Ripley's L/F/G point patterns, spatially variable genes by Moran's I / Geary's C, and permutation ligand-receptor tests (ligrec, OmniPath). Works on Visium spots and single-cell-resolution data (Xenium, MERFISH, CosMx, Slide-seq). Needs cluster or cell type labels for all but the spatially variable gene step. For an end-to-end ligand-receptor workflow use spatial-transcriptomics-cell-cell-communication.Testing★ 382
- 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.OfficialOther★ 31.9K
- spatial-transcriptomics-cell-type-annotationjaechang-hits/SciAgent-SkillsSpatial transcriptomics cell type annotation for single-cell-resolution platforms (Xenium, MERFISH, CosMx, SeqFISH): CELLxGENE reference download, Harmony label transfer, per-cluster marker evidence naming lineages then subtypes, spatial niches. Visium/Slide-seq spots: GPU -> spatial-transcriptomics-deconvolution-cell2location; CPU -> spatial-mapping-tangram (cell types: per-spot proportions); no reference -> spatial-domain-detection (regions: domains from markers). Beyond labels (microenvironment, arrangement, spatial patterns): read spatial-transcriptomics-analysis-squidpy before asking the user.Documents★ 382
- cell-type-annotationjaechang-hits/SciAgent-SkillsscRNA-seq cell type annotation - read before any annotation skills. Chooses and runs the route: name clusters manually from canonical markers (scanpy, runnable code here), transfer labels with CellTypist or a popV/scANVI on a reference, or do both and validate one against other. Covers package availability, tissue- and state-matched references, marker panels, confidence and marker validation of transferred labels, doublets, unresolved clusters. Tool-specific code lives in celltypist/popv-cell-annotation and scvi-tools-single-cell.Planning★ 382
Ratings & reviews
—
no reviews
Tried this skill? Rate it to help others. Sign in
Discussion
Join the discussion. Sign in