Identification of Disease-causative Variants for Clinical and Research Use

Rapidly identify clinically-relevant phenotype-associated genes and variants.

Quickly identify and curate variants to enable personalized patient care

Clinical Sequence Analyzer (CSA) allows users to quickly identify clinically-relevant phenotype-associated genes and variants from individual patients to complex families. Our novel data structure is engineered for both clinical diagnosis and research projects, and can scale with the massive data volumes from whole genome and whole exome sequence data.

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