PubMatcher: a web app to streamline genomic data interpretation with automated bibliographic research

In the era of rapidly accumulating genomic data, largely driven by the broad use of whole-genome sequencing (WGS) in clinical settings, interpreting lesser-known genes with varied phenotypes remains challenging. PubMatcher is a new tool that automates bibliographic research for multiple genes at once and grants quick and easy access to relevant gene information. It helps users efficiently identify potential genotype-phenotype associations using PubMed complemented by additional data. By significantly reducing analysis time, PubMatcher streamlines the interpretation of novel or under-documented genes. Available to non-commercial users for free, PubMatcher is a user-friendly and efficient solution for researchers, clinical scientists and pathologists working with pangenomics analyses.