An automated pipeline is developed that uses large language models to find single-gene perturbation experiments in NCBI-GEO and reconstruct their case-control sample groupings, along with the perturbed gene, perturbation type and cell line as structured, ontology-normalised fields.
Abstract
Public transcriptomic repositories contain thousands of gene perturbation experiments, a valuable resource for understanding gene function, but perturbation metadata are not structured, which blocks systematic reuse. Existing perturbation atlases depend on expert manual curation, so they are costly to maintain and infrequently updated, while automated grouping approaches neither identify which samples form the perturbation arm nor recover the perturbed gene. Here we develop an automated pipeline that uses large language models to find single-gene perturbation experiments in NCBI-GEO and reconstruct their case-control sample groupings, along with the perturbed gene, perturbation type and cell line as structured, ontology-normalised fields. We manually curated 3,300 GEO experiments with sample-level case-control assignments and release these as an open benchmark (2,400 training, 600 validation, 300 temporally held-out test). Reasoning models and task-specific finetuning substantially improved identification of valid perturbation groups, with the best model reaching precision 0.925 and recall 0.836 on the test set. Applied at scale, the pipeline generated an atlas of 6,802 gene perturbation expression signatures from 4,453 GEO experiments, covering 2,907 uniquely perturbed genes. An R package, perturbMatch, supports exploration of the atlas and querying of user-supplied expression signatures against it using similarity scoring, so users can identify experiments that recapitulate a transcriptional state of interest.
GEOMeta provides a scalable resource and reproducible framework for metadata curation in the Gene Expression Omnibus, and benchmarked transcriptome representation models for predicting sex, age, tissue and disease from transcriptome embeddings.
Xiaodan Zhang, S. Paithankar, Jing Pu et al.· bioRxiv· 0 citations
PxFquery provides a natural-language interface for exploring large-scale perturbation resources and enables their integration into diverse AI workflows and lowers the barrier to accessing these resources and enables their integration into diverse AI workflows.
An automated software tool to accomplish data curation tasks previously performed by humans for the Gemma genomics data re-analysis resource, with performance near that of human curators, at approximately 1/20th the cost and at least 100 times the speed.
P. Pavlidis, B. O. Mancarci, A. Mãximo et al.· bioRxiv· 0 citations
GenesetGPT is proposed, an efficient, LLM-based framework that emphasizes both curated biological context and iterative prompt construction, thus enabling realistic summarization of heterogeneous gene sets at scale.
Jack R. Leary, Samantha Pattey, Rhonda L. Bacher· bioRxiv· 0 citations
MKMC (Multi-sample Kmer Counter), a scalable, reference-free toolkit for RNA-seq analysis that leverages k-mer–based statistics to detect biological variation without requiring alignment, is presented.
L. Mboning, Maciej Dlugosz, Marek Kokot et al.· bioRxiv· 0 citations
This work establishes a controlled, extensible platform for benchmarking GRN reconstruction and single-cell analysis methods and introduces a flexible GRN generation script, allowing users to design or perturb regulatory networks to test specific hypotheses.
Unknown authors· 0 citations
We use cookies to run the site and, with your consent, for analytics and to show ads.
See our Cookie Policy.