bioinformatics-singlecell
About
This skill provides single-cell and multi-omic bioinformatics analysis for hematology and oncology, supporting workflows like scRNA-seq and CITE-seq. It enables key analyses including trajectory inference, batch correction, and differential expression using tools like Scanpy, scvi-tools, and Seurat. Use it for processing single-cell data from QC through to publication-ready figures with an emphasis on reproducible, interpretable outputs.
Quick Install
Claude Code
Recommendednpx skills add mdbabumiamssm/LLMs-Universal-Life-Science-and-Clinical-Skills- -a claude-code/plugin add https://github.com/mdbabumiamssm/LLMs-Universal-Life-Science-and-Clinical-Skills-git clone https://github.com/mdbabumiamssm/LLMs-Universal-Life-Science-and-Clinical-Skills-.git ~/.claude/skills/bioinformatics-singlecellCopy and paste this command in Claude Code to install this skill
GitHub Repository
Frequently asked questions
What is the bioinformatics-singlecell skill?
bioinformatics-singlecell is a Claude Skill by mdbabumiamssm. Skills package instructions and resources that Claude loads on demand, so Claude can perform bioinformatics-singlecell-related tasks without extra prompting.
How do I install bioinformatics-singlecell?
Use the install commands on this page: add bioinformatics-singlecell to Claude Code as a plugin, or clone its repository into your skills directory, then restart Claude so it picks up the skill.
What category does bioinformatics-singlecell belong to?
bioinformatics-singlecell is in the Other category, tagged automation and data.
Is bioinformatics-singlecell free to use?
Yes. bioinformatics-singlecell is listed on AIMCP and free to install. It runs inside Claude, so no separate service account is required to use the skill itself.
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