Click here to learn more about the CytoTerra^® Cytogenetics Platform:
features and benefits, applications, automated analytics, actionable results.

Click here to learn more about the ProxiMeta™ Metagenome Deconvolution Platform:
features and benefits, technology, applications, workflow, kits and cloud-based analysis.

Click here to learn more about the Proximo™ Genome Scaffolding Platform:
features and benefits, technology, applications, workflow, kits and analysis service.

Surpass the breadth and depth of karyotyping, FISH, and CMA with a single, NGS-based assay. The CytoTerra^® Platform enables high-resolution cytogenomic analysis of solid tumors—samples that are unsuitable for traditional cytogenetics.

The CytoTerra^® Platform uses proximity ligation technology to determine the structure of chromosomes from fresh-frozen or archival FFPE samples. In this case study, novel AML variants (undetected with traditional cytogenetics) impacted the risk stratification of 25% of samples.

The ProxiMeta™ Platform combines proximity ligation technology, short-read sequencing, and computational tools to generate genome-resolved metagenomes and host-linked mobile elements.

Unlike conventional metagenomics approaches, the ProxiMeta™ Platform enables genome-resolved metagenomics, accurate host attribution of mobile genetic elements, and metabolic analysis and functional characterization—directly from complex communities, without culturing.

The ProxiMeta™ Platform employs proximity ligation technology to significantly improve de novo binning and host attribution of bacterial and viral genomes recovered from complex metagenomic samples.

The ProxiMeta™ Platform unlocks the functional potential of metagenomic samples by enabling significantly improved annotation. This is accomplished through improvements in metagenome deconvolution, enabled by proximity ligation technology.

The Proximo™ Platform utilizes the ultra-long-range information provided by proximity ligation (Hi-C) to produce high-quality, highly contiguous genomes with full chromosomes and haplotype resolution.