Discover OncoTerra
Understanding the structure of our chromosomes is essential to understanding our health. Even though the human genome is the most studied genome of all life on earth, many questions remain unanswered by conventional sequencing and traditional cytogenomic methods.
Our OncoTerra® and CytoTerra® Platforms are enabled by Genomic Proximity Mapping (GPM)™, utilizing short-read sequencing data to map and measure the spatial relationship between any two loci across the full complement of chromosomes in a cell. Our advanced computational tools extract sequential information to construct ultra-long-range insights. This data is used to detect genetic variation and characterize all major types of chromosomal abnormalities, offering particular advantages for the study of cancer genomes.
Unlock another dimension in oncology and cytogenomics with scalable, low-cost ultra-long-range genome sequencing to ask and answer new biological questions, and help deliver on the promise of genomics in research and medicine.
