Skip to content
Back to skills

Omics

ASecurity

Skills for single-cell and spatial omics data analysis. Best practices, code snippets, and workflows for the scverse ecosystem.

  • 171 stars
  • 0 votes
  • 0 copies
  • 1 view
  • Added September 6, 2026
ai-agentsexpressapidatabaseperformance

Works with

  • cli
  • api

Security analysis

A100/100

Scanned September 6, 2026

npx -y skills add BioTender-max/awesome-bio-agent-skills --skill omics --agent claude-code

Installs into .claude/skills of the current project.

Are you the author of Omics?

Add the live security badge to your README. It updates with every re-scan.

Security grade badge for Omics
[![Security: A — Skills Directory](https://www.skillsdirectory.com/api/skills/biotender-max-omics/badge)](https://www.skillsdirectory.com/skills/biotender-max-omics)

More formats (shields.io, HTML) on the badges page. Keep it an A: scan every change in CI with Pro.

Download with Pro
SKILL.md
---
id: omics_skills_index
name: Omics Analysis Skills Index
description: |
  Skills for single-cell and spatial omics data analysis.
  Best practices, code snippets, and workflows for the scverse ecosystem.
---

# Agent Skills for Omics Data Analysis

Best practices and workflows for single-cell and spatial omics analysis.
Load the relevant skill files when performing specific analysis tasks.

## Core Single-Cell Skills

High-priority, actionable workflows for the most common single-cell analysis tasks.

**Skill index**: [single_cell/SKILL.md](./single_cell/SKILL.md)

**Skills**:
- **Quality Control**: Filtering, doublet detection, normalization, QC metrics
- **Cell Type Annotation**: Marker-based and reference-based label assignment
- **Trajectory Inference**: Pseudotime, lineage tracing, RNA velocity

---

## Gene Panel Selection

End-to-end workflow for designing gene panels in scRNA-seq and spatial
transcriptomics (HVG/DE/RF/scGeneFit/SpaPROS), with sub-panel discovery,
consensus scoring, biological completion, and benchmarking.

**Skill folder**: [gene_panel_selection/](./gene_panel_selection/)

**When to use**:
- Designing a gene panel for spatial transcriptomics
- Benchmarking existing panels (ARI/NMI/Silhouette + UMAP)
- **IMPORTANT**: When doing gene panel selection, **strictly** follow this workflow

---

## Spatial Omics

Skills for spatial transcriptomics mapping, imputation, and 3D visualization.

**Skill index**: [spatial/SKILL.md](./spatial/SKILL.md)

**Skills**:
- **Single-Cell to Spatial Mapping**: Map scRNA-seq to spatial data with MOSCOT
  for gene imputation and cell type transfer
- **3D Spatial Visualization**: Interactive 3D plots and rotating animations
  with PyVista

**When to use**:
- You have paired scRNA-seq and spatial transcriptomics data
- You want to impute genes or transfer cell type labels to spatial coordinates
- Your spatial data has 3D coordinates and you want to visualize them

---

## Single-Cell Foundation Models (SCFM)

Workflow and model reference for embedding/integration with foundation models
(scGPT, Geneformer, UCE, scBERT, etc.).

**Skill index**: [scfm/SKILL.md](./scfm/SKILL.md)

**When to use**:
- You want FM embeddings (e.g., `obsm["X_uce"]`, `obsm["X_scGPT"]`)
- You need model selection based on gene ID scheme and species
- You want a validation-first workflow before heavy inference

---

## Database Access

Tools for querying genomic databases, downloading sequencing data, and
accessing large-scale single-cell datasets programmatically.

**Skill index**: [database_access/SKILL.md](./database_access/SKILL.md)

**Tools covered**:
- **gget**: 23 modules for querying Ensembl, NCBI, UniProt, COSMIC, OpenTargets, etc.
- **iSeq**: CLI for downloading from GSA, SRA, ENA, DDBJ, GEO
- **CZ CELLxGENE Census**: API for 217M+ single-cell observations

---

## Upstream Processing

Technology-specific pipelines for processing raw sequencing data into
analysis-ready count matrices.

**Skill index**: [upstream_processing/SKILL.md](./upstream_processing/SKILL.md)

**Technologies covered**:
- **nf-core Pipelines**: 143+ Nextflow pipelines for scRNA-seq, spatial, bulk,
  ATAC-seq, ChIP-seq, variant calling
- **OpenST**: Open-source spatial transcriptomics processing pipeline

---

## General Data Analysis

Cross-cutting skills for environment setup and computational performance.

**Skill index**: [general_data_analysis/SKILL.md](./general_data_analysis/SKILL.md)

**Skills**:
- **Environment Management**: Conda/Mamba/venv setup for reproducible environments
- **Parallel Computing**: Multi-core CPU, GPU acceleration, memory optimization

---

## Supplementary Reference: SC Best Practices

Comprehensive guidance derived from the
[Single-cell Best Practices](https://www.sc-best-practices.org) book.
Use as supplementary context when the core skills above need deeper background.

**Skill index**: [sc_best_practices/SKILL.md](./sc_best_practices/SKILL.md)

**Topics covered**:
- Preprocessing, normalization, dimensionality reduction
- Clustering, annotation, dataset integration
- Trajectory analysis, RNA velocity, lineage tracing
- Differential expression, compositional analysis, pathway analysis
- Gene regulatory networks, cell-cell communication
- Bulk deconvolution, scATAC-seq, spatial omics
- CITE-seq, immune repertoire (TCR/BCR)
- Multimodal integration, reproducibility

---

## Using Skills

1. **Before analysis**: Scan this index for relevant skills
2. **Load skill file**: Read the full skill document for detailed guidance
3. **Follow best practices**: Use the code snippets and workflows provided
4. **Adapt as needed**: Skills are templates; adjust for your specific data

Attribution

Is this your skill, or is something wrong with this listing? Request removal or report an issue. Author removals are honored within 72 hours.

Comments

Loading comments…