De la autor
RNA velocity analysis with scVelo. Estimate cell state transitions from unspliced/spliced mRNA dynamics, infer trajectory directions, compute latent time, and identify driver genes in single-cell RNA-seq data. Complements Scanpy/scVI-tools for trajectory inference.
Instalare
npx skills add BioTender-max/awesome-bio-agent-skills --skill scvelo -a claude-code
Se instalează în .claude/skills/scvelo/ · Fiecare comandă descarcă skill-ul direct de pe GitHub cu utilitarul open source skills.
Descarcă .zip
Identic octet cu octet cu commit-ul scanat, cu licența depozitului și un fișier SOURCE.txt.
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Verificări de siguranță pe SKILL.md
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De ce 74
Securitate85
Proveniență68
Întreținere70
Licență100
Adopție39
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Skill-uri similare
Cele mai apropiate de acesta prin ce fac și când sunt folosite.
- alterlab-scveloAlterLab-IEU/AlterLab-Academic-SkillsRun 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.Altele★ 85
- 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★ 56.2K
- trajectory-analysisawslabs/hcls-agent-skillsSingle-cell trajectory inference pipeline covering diffusion pseudotime (DPT), PAGA, RNA velocity with scVelo, and fate mapping with CellRank. Use when the user mentions pseudotime, trajectory, lineage, differentiation, RNA velocity, scVelo, CellRank, PAGA, diffusion map, fate probabilities, terminal states, spliced/unspliced, velocyto, order cells by development, cell differentiation path, cell fate, branching analysis, monocle, developmental trajectory, stem cell differentiation, progenitor to mature, how do cells differentiate, cell lineage tree, velocity arrows, fate mapping, transition probabilities, root cells, terminal states, absorption probabilities, or latent time.Altele★ 72
- trajectory-inferencejaechang-hits/SciAgent-SkillsTrajectory inference and cell fate mapping for single-cell and spatial transcriptomics: PAGA graph + diffusion pseudotime (no velocity needed), scVelo RNA velocity (stochastic / dynamical, from spliced/unspliced counts), CellRank 2 terminal states, fate probabilities and lineage drivers, then pseudotime and fates mapped on tissue with a spatial autocorrelation check. Outputs pseudotime, velocity streams, fate probability tables. Imaging panels (Xenium, MERFISH) have no unspliced counts: use PAGA/DPT or the CellRank pseudotime kernel. For a basic PAGA recipe inside a standard scRNA-seq workflow see scanpy-scrna-seq.Productivitate★ 385
- 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★ 34.8K
- scrna-seq-pipelineawslabs/hcls-agent-skillsScanpy-based single-cell RNA-seq analysis pipeline covering loading (10X, h5ad), QC, normalization, HVG selection, PCA/UMAP, Leiden clustering, differential expression, and batch correction (Harmony, scVI). Use when the user mentions single-cell, scRNA-seq, Scanpy, AnnData, UMAP, clustering, 10X, h5ad, leiden, highly variable genes, Harmony, scVI, cluster cells, find marker genes, filter low-quality cells, gene expression matrix, doublet removal, normalize counts, dimensionality reduction, cell clustering, QC single-cell, filtered_feature_bc_matrix, cellranger output, 10X h5, scrublet, cell ranger, count matrix, find cell types, batch effect, integration, neighborhood graph, or differential expression genes.Altele★ 72
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