We investigated whether LLMs can prioritize disease-associated genes as well or better than dedicated bioinformatics methods relying on phenotype similarity. This repository contains all the data and code that we used in this study.
Data: This folder contains all the input datasets and internediate files needed to run the scipts. See the readme file in this fodler for details.
Code: This folder contains all the scripts. See the readme file in this folder for details.