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Our leaders are pioneers of genetic research and clinical applications. They are deeply committed to scientific accessibility, data, and community.
Two University of Cambridge chemists receive one of the world’s highest honors in science and technology
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Maximize identification of molecularly matched therapies with one biopsy, one test, one report
Cancer Research Products
Microbial Genomics Research
Partnership allows researchers to sequence hundreds of organisms and process data faster
Microbial Genomics Products
Dr. Bertram Brenig uses genomics grant to help save the bees
The continent with the highest amount of genetic diversity is underrepresented in global genomic databases
Complex Disease Research Products
The collaboration will introduce VeriSeq NIPT Solution v2 in Southeast Asia
Reproductive Health Products
Genomic Answers for Kids project will use NGS for families who have undergone many tests without progress
Genetic Health Products
The Illumina Connected Analytics (ICA) platform is the foundation on which a customized genomics analysis environment is built, managing and processing large amounts of heterogenous data sets.
The DRAGEN platform calls both small and large variants from population genetics studies with high precision and speed.
DRAGEN recently won the PrecisionFDA Truth Challenge V2 contest for Illumina reads in the Difficult-to-Map and All-Benchmark Regions categories.
SMNCopyNumberCaller enables accurate copy number calling of the highly similar SMN1 and SMN2 for spinal muscular atrophy diagnosis/carrier screening.
SpliceAI, a 32-layer deep neural network, predicts splicing from pre-mRNA sequences and identifies cryptic splice variants in rare disease patients.
REViewer is a computational method for visualization of sequencing data in genomic regions containing long repeat expansions.
CYP2D6 metabolizes 21% of clinically used drugs. Cyrius resolves common SVs and sequence homology to paralog and genotypes CYP2D6 with 99.3% accuracy.
Paragraph is a graph aligner and variant caller that can accurately genotype known structural variants using the aligned sequence reads.
The Illumina team developed deep neural network algorithm, PrimateAI, to predict the clinical impact of human missense mutations.