Emergent Mind

Abstract

Interrogation of biological pathways is an integral part of omics data analysis. LLMs enable the generation of custom pathways and gene sets tailored to specific scientific questions. These targeted sets are significantly smaller than traditional pathway enrichment analysis libraries, reducing multiple hypothesis testing and potentially enhancing statistical power. Lomics (LLMs for Omics Studies) v1.0 is a python-based bioinformatics toolkit that streamlines the generation of pathways and gene sets for transcriptomic analysis. It operates in three steps: 1) deriving relevant pathways based on the researcher's scientific question, 2) generating valid gene sets for each pathway, and 3) outputting the results as .GMX files. Lomics also provides explanations for pathway selections. Consistency and accuracy are ensured through iterative processes, JSON format validation, and HUGO Gene Nomenclature Committee (HGNC) gene symbol verification. Lomics serves as a foundation for integrating LLMs into omics research, potentially improving the specificity and efficiency of pathway analysis.

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