Accelerating genomics variant interpretation with AWS HealthOmics and Amazon Bedrock AgentCore
Genomic research stands at a transformative crossroads where the exponential growth of sequencing data demands equally sophisticated analytical capabilities. According to the 1000 Genomes Project, a typical human genome differs from the reference at 4.1–5.0 million sites, with most variants being SNPs and short indels. These variants, when aggregated across individuals, contribute to differences in…


