mcpbeat Sign in

Scvelo Agent Skill

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.

2.7k tokens
context cost
SKILL.md, read when the skill is used
3
files
ships runnable scripts
1
copies elsewhere
how many repositories repackaged it
32 514
stars on the repo
on the repository, not the skill itself

Install

one command, takes just this skill from the repository
npx skills add https://github.com/K-Dense-AI/scientific-agent-skills --skill scvelo

The instruction itself

19 sections, as written by the author

scVelo — RNA Velocity Analysis

Overview

scVelo is the leading Python package for RNA velocity analysis in single-cell RNA-seq data. It infers cell state transitions by modeling the kinetics of mRNA splicing — using the ratio of unspliced (pre-mRNA) to spliced (mature mRNA) abundances to determine whether a gene is being upregulated or downregulated in each cell. This allows reconstruction of developmental trajectories and identification of cell fate decisions without requiring time-course data.

Installation: uv pip install scvelo

Key resources:

  • Documentation: https://scvelo.readthedocs.io/
  • GitHub: https://github.com/theislab/scvelo
  • Paper: Bergen et al. (2020) Nature Biotechnology. PMID: 32747759

When to Use This Skill

Use scVelo when:

  • Trajectory inference from snapshot data: Determine which direction cells are differentiating
  • Cell fate prediction: Identify progenitor cells and their downstream fates
  • Driver gene identification: Find genes whose dynamics best explain observed trajectories
  • Developmental biology: Model hematopoiesis, neurogenesis, epithelial-to-mesenchymal transitions
  • Latent time estimation: Order cells along a pseudotime derived from splicing dynamics
  • Complement to Scanpy: Add directional information to UMAP embeddings

Prerequisites

scVelo requires count matrices for both unspliced and spliced RNA. These are generated by:

  • STARsolo or kallisto|bustools with lamanno mode
  • velocyto CLI: velocyto run10x / velocyto run
  • alevin-fry / simpleaf with spliced/unspliced output

Data is stored in an AnnData object with layers["spliced"] and layers["unspliced"].

Standard RNA Velocity Workflow

1. Setup and Data Loading

import scvelo as scv
import scanpy as sc
import numpy as np
import matplotlib.pyplot as plt

# Configure settings
scv.settings.verbosity = 3       # Show computation steps
scv.settings.presenter_view = True
scv.settings.set_figure_params('scvelo')

# Load data (AnnData with spliced/unspliced layers)
# Option A: Load from loom (velocyto output)
adata = scv.read("cellranger_output.loom", cache=True)

# Option B: Merge velocyto loom with Scanpy-processed AnnData
adata_processed = sc.read_h5ad("processed.h5ad")  # Has UMAP, clusters
adata_velocity = scv.read("velocyto.loom")
adata = scv.utils.merge(adata_processed, adata_velocity)

# Verify layers
print(adata)
# obs × var: N × G
# layers: 'spliced', 'unspliced' (required)
# obsm['X_umap'] (required for visualization)

2. Preprocessing

# Filter and normalize. As of scVelo 0.3, filter_and_normalize() only filters
# genes and normalizes per cell -- it no longer takes n_top_genes and no longer
# log-transforms, so the log step and HVG selection come from Scanpy.
scv.pp.filter_and_normalize(
    adata,
    min_shared_counts=20    # Minimum counts in spliced+unspliced
)
sc.pp.log1p(adata)
sc.pp.highly_variable_genes(adata, n_top_genes=2000, subset=True)

# Compute first and second order moments (means and variances)
# knn_connectivities must be computed first
sc.pp.neighbors(adata, n_neighbors=30, n_pcs=30)
scv.pp.moments(
    adata,
    n_pcs=30,
    n_neighbors=30
)

3. Velocity Estimation — Stochastic Model

The stochastic model is fast and suitable for exploratory analysis:

# Stochastic velocity (faster, less accurate)
scv.tl.velocity(adata, mode='stochastic')
scv.tl.velocity_graph(adata)

# Visualize
scv.pl.velocity_embedding_stream(
    adata,
    basis='umap',
    color='leiden',
    title="RNA Velocity (Stochastic)"
)

The dynamical model fits the full splicing kinetics and is more accurate:

# Recover dynamics (computationally intensive; ~10-30 min for 10K cells)
scv.tl.recover_dynamics(adata, n_jobs=4)

# Compute velocity from dynamical model
scv.tl.velocity(adata, mode='dynamical')
scv.tl.velocity_graph(adata)

5. Latent Time

The dynamical model enables computation of a shared latent time (pseudotime):

# Compute latent time
scv.tl.latent_time(adata)

# Visualize latent time on UMAP
scv.pl.scatter(
    adata,
    color='latent_time',
    color_map='gnuplot',
    size=80,
    title='Latent time'
)

# Identify top genes ordered by latent time
top_genes = adata.var['fit_likelihood'].sort_values(ascending=False).index[:300]
scv.pl.heatmap(
    adata,
    var_names=top_genes,
    sortby='latent_time',
    col_color='leiden',
    n_convolve=100
)

6. Driver Gene Analysis

# Identify genes with highest velocity fit
scv.tl.rank_velocity_genes(adata, groupby='leiden', min_corr=0.3)
df = scv.DataFrame(adata.uns['rank_velocity_genes']['names'])
print(df.head(10))

# Speed and coherence
scv.tl.velocity_confidence(adata)
scv.pl.scatter(
    adata,
    c=['velocity_length', 'velocity_confidence'],
    cmap='coolwarm',
    perc=[5, 95]
)

# Phase portraits for specific genes
scv.pl.velocity(adata, ['Cpe', 'Gnao1', 'Ins2'],
               ncols=3, figsize=(16, 4))

7. Velocity Arrows and Pseudotime

# Arrow plot on UMAP
scv.pl.velocity_embedding(
    adata,
    arrow_length=3,
    arrow_size=2,
    color='leiden',
    basis='umap'
)

# Stream plot (cleaner visualization)
scv.pl.velocity_embedding_stream(
    adata,
    basis='umap',
    color='leiden',
    smooth=0.8,
    min_mass=4
)

# Velocity pseudotime (alternative to latent time)
scv.tl.velocity_pseudotime(adata)
scv.pl.scatter(adata, color='velocity_pseudotime', cmap='gnuplot')

8. PAGA Trajectory Graph

# PAGA graph with velocity-informed transitions
scv.tl.paga(adata, groups='leiden')
df = scv.get_df(adata, 'paga/transitions_confidence', precision=2).T
df.style.background_gradient(cmap='Blues').format('{:.2g}')

# Plot PAGA with velocity
scv.pl.paga(
    adata,
    basis='umap',
    size=50,
    alpha=0.1,
    min_edge_width=2,
    node_size_scale=1.5
)

Complete Workflow Script

import scvelo as scv
import scanpy as sc

def run_rna_velocity(adata, n_top_genes=2000, mode='dynamical', n_jobs=4):
    """
    Complete RNA velocity workflow.

    Args:
        adata: AnnData with 'spliced' and 'unspliced' layers, UMAP in obsm
        n_top_genes: Number of top HVGs for velocity
        mode: 'stochastic' (fast) or 'dynamical' (accurate)
        n_jobs: Parallel jobs for dynamical model

    Returns:
        Processed AnnData with velocity information
    """
    scv.settings.verbosity = 2

    # 1. Preprocessing (scVelo 0.3 dropped log/HVG from filter_and_normalize)
    scv.pp.filter_and_normalize(adata, min_shared_counts=20)
    sc.pp.log1p(adata)
    sc.pp.highly_variable_genes(adata, n_top_genes=n_top_genes, subset=True)

    if 'neighbors' not in adata.uns:
        sc.pp.neighbors(adata, n_neighbors=30)

    scv.pp.moments(adata, n_pcs=30, n_neighbors=30)

    # 2. Velocity estimation
    if mode == 'dynamical':
        scv.tl.recover_dynamics(adata, n_jobs=n_jobs)

    scv.tl.velocity(adata, mode=mode)
    scv.tl.velocity_graph(adata)

    # 3. Downstream analyses
    if mode == 'dynamical':
        scv.tl.latent_time(adata)
        scv.tl.rank_velocity_genes(adata, groupby='leiden', min_corr=0.3)

    scv.tl.velocity_confidence(adata)
    scv.tl.velocity_pseudotime(adata)

    return adata

Key Output Fields in AnnData

After running the workflow, the following fields are added:

| Location | Key | Description |

|----------|-----|-------------|

| adata.layers | velocity | RNA velocity per gene per cell |

| adata.layers | fit_t | Fitted latent time per gene per cell |

| adata.obsm | velocity_umap | 2D velocity vectors on UMAP |

| adata.obs | velocity_pseudotime | Pseudotime from velocity |

| adata.obs | latent_time | Latent time from dynamical model |

| adata.obs | velocity_length | Speed of each cell |

| adata.obs | velocity_confidence | Confidence score per cell |

| adata.var | fit_likelihood | Gene-level model fit quality |

| adata.var | fit_alpha | Transcription rate |

| adata.var | fit_beta | Splicing rate |

| adata.var | fit_gamma | Degradation rate |

| adata.uns | velocity_graph | Cell-cell transition probability matrix |

Velocity Models Comparison

| Model | Speed | Accuracy | When to Use |

|-------|-------|----------|-------------|

| stochastic | Fast | Moderate | Exploratory; large datasets |

| deterministic | Medium | Moderate | Simple linear kinetics |

| dynamical | Slow | High | Publication-quality; identifies driver genes |

Best Practices

  • Start with stochastic mode for exploration; switch to dynamical for final analysis
  • Need good coverage of unspliced reads: Short reads (< 100 bp) may miss intron coverage
  • Minimum 2,000 cells: RNA velocity is noisy with fewer cells
  • Velocity should be coherent: Arrows should follow known biology; randomness indicates issues
  • k-NN bandwidth matters: Too few neighbors → noisy velocity; too many → oversmoothed
  • Sanity check: Root cells (progenitors) should have high unspliced/spliced ratios for marker genes
  • Dynamical model requires distinct kinetic states: Works best for clear differentiation processes

Troubleshooting

| Problem | Solution |

|---------|---------|

| Missing unspliced layer | Re-run velocyto or use STARsolo with --soloFeatures Gene Velocyto |

| Very few velocity genes | Lower min_shared_counts; check sequencing depth |

| Random-looking arrows | Try different n_neighbors or velocity model |

| Memory error with dynamical | Set n_jobs=1; reduce n_top_genes |

| Negative velocity everywhere | Check that spliced/unspliced layers are not swapped |

Additional Resources

  • scVelo documentation: https://scvelo.readthedocs.io/
  • Tutorial notebooks: https://scvelo.readthedocs.io/tutorials/
  • GitHub: https://github.com/theislab/scvelo
  • Paper: Bergen V et al. (2020) Nature Biotechnology. PMID: 32747759
  • velocyto (preprocessing): http://velocyto.org/
  • CellRank (fate prediction, extends scVelo): https://cellrank.readthedocs.io/
  • dynamo (metabolic labeling alternative): https://dynamo-release.readthedocs.io/

Other skills for the same job

different authors, same section of the catalogue
Skill Creator
by anthropics
vendor ×12

Create new skills, modify and improve existing skills, and measure skill performance. Use when users want to create a skill from scratch, edit, or optimize an existing skill, run evals to test a skill, benchmark skill performance with variance analysis, or optimize a skill's description for better triggering accuracy.

8.3k tokens scripts
Geo Database
by christophacham
×4

Access NCBI GEO for gene expression/genomics data. Search/download microarray and RNA-seq datasets (GSE, GSM, GPL), retrieve SOFT/Matrix files, for transcriptomics and expression analysis.

6.3k tokens
Pymc Bayesian Modeling
by christophacham
×4

Bayesian modeling with PyMC. Build hierarchical models, MCMC (NUTS), variational inference, LOO/WAIC comparison, posterior checks, for probabilistic programming and inference.

4.2k tokens scripts
Pymoo
by christophacham
×4

Multi-objective optimization framework. NSGA-II, NSGA-III, MOEA/D, Pareto fronts, constraint handling, benchmarks (ZDT, DTLZ), for engineering design and optimization problems.

4.4k tokens scripts
Statsmodels
by ComeOnOliver
×4

Statistical modeling toolkit. OLS, GLM, logistic, ARIMA, time series, hypothesis tests, diagnostics, AIC/BIC, for rigorous statistical inference and econometric analysis.

4.9k tokens
Add Uint Support
by pytorch
vendor ×3

Add unsigned integer (uint) type support to PyTorch operators by updating AT_DISPATCH macros. Use when adding support for uint16, uint32, uint64 types to operators, kernels, or when user mentions enabling unsigned types, barebones unsigned types, or uint support.

2.3k tokens
At Dispatch V2
by pytorch
vendor ×3

Convert PyTorch AT_DISPATCH macros to AT_DISPATCH_V2 format in ATen C++ code. Use when porting AT_DISPATCH_ALL_TYPES_AND*, AT_DISPATCH_FLOATING_TYPES*, or other dispatch macros to the new v2 API. For ATen kernel files, CUDA kernels, and native operator implementations.

2.2k tokens
Docstring
by pytorch
vendor ×3

Write docstrings for PyTorch functions and methods following PyTorch conventions. Use when writing or updating docstrings in PyTorch code.

2.6k tokens

How to use it

Copy the folder

Take k-dense-ai/scvelo from the repository into ~/.claude/skills for personal use, or into .claude/skills inside a project.

Check the name does not clash

The agent identifies a skill by the name field in its header. Two skills with the same name cannot sit side by side — one of them will be ignored.

Install what it needs

The instructions reference pip, uv. Without those the skill loads but fails at the first command.