arxiv-database
This skill provides Python tools for searching and retrieving preprints from arXiv.org via its public Atom API. It supports keyword search,…
Maintainer FreedomIntelligence · Last updated April 1, 2026
Perform differential expression analysis using edgeR in R/Bioconductor. Use for analyzing RNA-seq count data with the quasi-likelihood F-test framework, creating DGEList objects, normalization, dispersion estimation, and statistical testing. Use when performing DE analysis with edgeR.
Original source
https://github.com/FreedomIntelligence/OpenClaw-Medical-Skills/tree/main/skills/bio-de-edger-basics
Skill Snapshot
Source Doc
Goal: Construct an edgeR container from a count matrix with sample group information.
Approach: Wrap raw counts and group labels into a DGEList object for normalization and testing.
"Load my RNA-seq counts into edgeR" → Create a DGEList from a count matrix with sample group assignments and optional gene annotations.
## With gene annotation
y <- DGEList(counts = counts, group = group, genes = gene_info)
## Standard edgeR Workflow (Quasi-Likelihood)
**Goal:** Run the complete edgeR QL pipeline from raw counts to differentially expressed gene lists.
**Approach:** Filter, normalize (TMM), estimate dispersions, fit quasi-likelihood GLM, and test coefficients with the QL F-test.
**"Find differentially expressed genes between my groups"** → Test for significant expression differences using negative binomial models with quasi-likelihood F-tests.
```r
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