Abstract
<jats:p>Purpose: We introduce GraNPA, standing for Graph Node-Phenotype Associa- tion, a method performing a GWAS-like analysis on a pangenome variation graph (PVG) built using a small number of individual genome sequences, without the need for additional population materials or kinship information for qualitative phenotypes. This method reduces the number of individuals required for associ- ation studies and prevents reference bias from variant calling in these types of analyses. Background: A PVG represents the multiple alignment of a set of complete genomes. It contains all variations, from single nucleotide polymorphisms (SNPs) to large structural variations (SVs), which are represented as nodes in the graph. By integrating phenotype information within nodes, we can assign a Phenotype Score (PS) to each node in the PVG and identify phenotype-related regions directly within it. These regions represent statistically significant shifts in PS distribution, highlighting their implication in the phenotype. Finally, GraNPA provides their positions and scores for further analysis. Results: This method was tested using simulated data and two publicly available datasets: the Sub1A gene locus for Oryza sativa in a 13 indi- viduals PVG, and the insertion responsible for the white-headed cattle with a PVG of 24 individuals. Source code of GraNPA is available here https://forge.ird.fr/diade/graphgwas/granpa under GNU GPLv3. Conclusion: GraNPA was able to identify the expected area in two simulated datasets and the responsible loci for these two known traits using only a few 1 dozen complete genomes in these PVGs. While currently limited to qualitative phenotypes, this method opens the way to more efficient ones relying on PVGs and few individuals.</jats:p>