New study demonstrates up to 73% reduction in genome analysis errors using AI-trained models versus standard approaches

SAN JOSE, Calif., April 29, 2026 – Complete Genomics, a U.S.-based leader in genomic sequencing technologies, today announced results demonstrating that AI-trained variant calling models can reduce genome analysis errors by up to 73% when applied to DNBSEQ™ sequencing data generated on its advanced massively parallel sequencing platform compared to widely used industry standard pipelines.