We are delighted to announce that bioXcelerate AI’s innovative work was showcased at the prestigious European Society of Human Genetics (ESHG) Conference in Berlin. The ESHG event is a key platform for geneticists from Europe and around the world to share breakthroughs and advancements in human genetics research.
At the conference, Dr. Heiko Runz, a scientific partner of bioXcelerate, presented our pioneering isGWAS solution—an ultra-high-throughput, scalable, and equitable platform for inferring genetic associations with disease. This groundbreaking in-silico genome-wide association (isGWAS) technique uses a cutting-edge statistical algorithm to transform the time-consuming nature of traditional GWAS into a process that takes mere minutes.
isGWAS enables researchers to examine whole-genome sequencing data from millions of individuals without the need for access to individual-level data. Its computational efficiency, paired with its scalability, accelerates discoveries in human genetics while maintaining equitable access to large-scale biobank data. Additionally, isGWAS supports biobank design by predicting disease associations for any sample size, helping to drive impactful insights across a wide range of studies.
By leveraging this innovative platform, bioXcelerate is empowering researchers to fast-track genetic research and drive impactful discoveries in the field of human genetics.
Contact us here to learn more about how isGWAS can support your research.