Universal Single Cell AnnotatorSAFE
The largest open-source medical AI skills library for OpenClaw🦞.
Overview
From the repository's own README, as read at the audited commit. Badges and raw HTML are left out.
- Project Name: Single Cell Annotation by cellidentifierdx.
- Description: Annotate your single cell using cellidentifierd.
- Installation: Instructions for how to install your project.
- Usage: Instructions for how to use your project after it's installed.
- License: The license your project is distributed under.
- Note: This software package is yet to be published (unpublished)! If you have used it for publication purpose, please share authorship with MD. BABU MIA, PHD; ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI. Contact for detials: [email protected]
CellIdentifierDX is a Python package for identifying cell types using Bayesian scoring.
Installation
You can install CellIdentifierDX using pip:
pip install cellidentifierdx
Usage
Here's a basic example of how to use --> Extract 250 genes per cluster: #getting to gene lists - step 2 continue import os import numpy as np import pandas as pd import anndata import scanpy as sc import scvi import scipy.io import matplotlib.pyplot as plt
Perform differential expression analysis
sc.tl.rankgenesgroups(combinedadata, groupby="leidenscvi", keyadded="rankgenes", method="t-testoverestimvar", n_genes=250)
Extract marker genes for each cluster along with their scores, fold changes, and p-values
markergenes250 = pd.DataFrame(combinedadata.uns['rankgenes']['names']).head(250) markerscores250 = pd.DataFrame(combinedadata.uns['rankgenes']['scores']).head(250) markerlogfoldchanges250 = pd.DataFrame(combinedadata.uns['rankgenes']['logfoldchanges']).head(250) markerpvals250 = pd.DataFrame(combine
29f31a89230cOBSERVED · 2026-10-08Install
Commands as the repository documents them. They are shown, not run.
pip install cellidentifierdx
What it tells the agent
The instruction file, verbatim from the audited commit — this is the text the model reads, and the surface the audit's instruction layer examines. Quoted here so you can judge it without cloning anything.
<!-- # COPYRIGHT NOTICE # This file is part of the "Universal Biomedical Skills" project. # Copyright (c) 2026 MD BABU MIA, PhD <[email protected]> # All Rights Reserved. # # This code is proprietary and confidential. # Unauthorized copying of this file, via any medium is strictly prohibited. # # Provenance: Authenticated by MD BABU MIA --> --- name: 'universal-single-cell-annotator' description: 'Annotate scRNA-seq' measurable_outcome: Execute skill workflow successfully with valid output within 15 minutes. allowed-tools: - read_file - run_shell_command --- # Universal Single-Cell Annotator This skill wraps multiple cell type annotation strategies into a single Python class. It allows agents to flexibly choose between rule-based (markers), data-driven (CellTypist), or reasoning-based (LLM) approaches depending on the context. ## When to Use This Skill * **Initial Analysis**: When processing raw AnnData objects. * **Validation**: When cross-referencing automated labels with known markers. * **Discovery**: When identifying rare cell types using LLM reasoning on marker lists. ## Core Capabilities 1. **Marker-Based Scoring**: Scores cells based on provided gene lists (e.g., "T-cell": ["CD3D", "CD3E"]). 2. **Deep Learning Reference**: Wraps `celltypist` to transfer labels from massive atlases. 3. **LLM Reasoning**: Extracts top markers per cluster and constructs prompts for LLM interpretation. ## Workflow 1. **Load Data**: Ensure data is in `AnnData` format (standard for Scanpy). 2. **Choose Strategy**: * Use **Markers** if you have a known gene panel. * Use **CellTypist** for broad immune/tissue profiling. * Use **LLM** for novel clusters. 3. **Annotate**: Run the corresponding method. 4. **Inspect**: Check `adata.obs` for the new annotation columns. ## Example Usage **User**: "Annotate this dataset looking for T-cells and B-cells." **Agent Action**: ```python from universal_annotator import UniversalAnnotator import scanpy as sc adata = sc.read_h5ad('data.h5ad') annotator = UniversalAnnotator(adata) markers = { 'T-cell': ['CD3D', 'CD3E', 'CD8A'], 'B-cell': ['CD79A', 'MS4A1'] } annotator.annotate_marker_based(markers) # Results in adata.obs['predicted_cell_type'] ``` <!-- AUTHOR_SIGNATURE: 9a7f3c2e-MD-BABU-MIA-2026-MSSM-SECURE -->
Trust audit
SAFEgrade B · trust 89/100 Nothing in the source contradicts what it says it does. Grade A is reserved for packages that have also passed the behavioural sandbox.
| Layer | What it checks | Result |
|---|---|---|
| L0 | Provenance & inventory | PASS |
| L1 | Static analysis of the code | PASS |
| L2 | Instruction surface (what it tells the agent) | PASS |
| L3 | Class-specific surface | PASS |
| L4 | Behavioural (sandbox) | SKIPPED |
What the source does
- Filesystem
- none-observed
- Network
- none-observed
- Shell
- none-observed
- Dependencies
- pinned
- Secrets in source
- none-found
Findings (1)
Gates applied: no_behavioural_pass.
29f31a89230cfull audit observations/trust-audit/skill/freedomintelligence__universal-single-cell-annotator.json · Report an issue / request a re-scanAudit history
Every audit this skill has had.
| Date | Source | Verdict | Grade | Score | Change |
|---|---|---|---|---|---|
| 2026-10-08 | 29f31a89230c | SAFE | B | 89 | first audit |
Questions
What does the Universal Single Cell Annotator skill do?
The largest open-source medical AI skills library for OpenClaw🦞.
Is Universal Single Cell Annotator safe to install?
The audit found nothing in the source that contradicts what it says it does, and graded it B (89/100). Grade A is held back for packages that have also passed a sandboxed behavioural run, which is why a clean skill reads B.
What can Universal Single Cell Annotator access on my machine?
The audit observed no filesystem, network or shell use at all in its source.
How current is this page?
The grade is for one exact copy of the source (29f31a89230c), read on 2026-10-08. The repository is watched, and a new audit runs when it changes — this is the first audit.