Abstract
An embodiment relates to a polygenic risk score visualization method. The method includes confirming whether input genotype data matches prestored genetic variation risk data and mapping genes and genetic variants based on the genotype data, calculating a polygenic risk score, attributed values, and variant contribution scores for the genetic variants based on a plurality of preset algorithms, and providing visualization by visualizing gene contribution scores for each gene at a population level, attributed values for each gene at an individual level, and variant contribution scores for each gene at an individual level based on the attributed values and the variant contribution scores.
Full Text
What is claimed is:
An embodiment relates to a polygenic risk score visualization method. The method includes confirming whether input genotype data matches prestored genetic variation risk data and mapping genes and genetic variants based on the genotype data, calculating a polygenic risk score, attributed values, and variant contribution scores for the genetic variants based on a plurality of preset algorithms, and providing visualization by visualizing gene contribution scores for each gene at a population level, attributed values for each gene at an individual level, and variant contribution scores for each gene at an individual level based on the attributed values and the variant contribution scores.
Timeline
Filed
05/06/2026Published
09/10/2026Granted
Not AvailableIPC Codes(5)
G16H 50/30:for calculating health indices; for individual health risk assessment
G16B 20/20:Allele or variant detection, e.g. single nucleotide polymorphism [SNP] detection
G16B 45/00:ICT specially adapted for bioinformatics-related data visualisation, e.g. displaying of maps or networks