knomeDISCOVERY: Genome interpretation tools and services for researchers

An end-to-end solution, including sequencing, curation, informatics, and interpretation.

knomeDISCOVERY is a human genome interpretation service. It includes whole genome sequencing (optional), project-driven curation, sophisticated informatics, and in-depth interpretation by a team of highly experienced geneticists. knomeDISCOVERY is for academic, medical, and pharmaceutical research studies of 10s to 1,000s of genomes.


Interpretation-ready data and advanced software tools for identifying causal variants and pathways.

knomeBASE provides the informatics and software tools that geneticists need to quickly identify candidate causal variants, genes, and gene sets.

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