The Variantyx Difference
Our genomic technologies enable precision medicine
Practicing at the top of your scope requires the best tools. Whether you serve patients in reproductive genetics, rare genetic disorders, or precision oncology, our unique blend of whole genome sequencing (WGS) and proprietary software platforms provide superior genomic tools.
The power of a whole genome sequencing platform
Whether you want to a custom analysis, a gene panel, the exome, or genome, our PCR-free WGS platform provides high-quality data for in-depth analyses. Removing the PCR amplification step means your patient’s data has uniform coverage across ~98% of the genome. This leads to one of the highest diagnostic rates for a single test compared to other testing technologies.1
Source: 100,000 Genomes Project Pilot Investigators. PMID: 34758253.In one large WGS study, clinicians reported that 25% of [rare] genetic diagnoses (134 of the 533) had ‘immediate clinical actionability.’’1
Introducing long-read sequencing
Our commitment to providing the most comprehensive and accurate genetic testing solutions means continually pushing technology boundaries. With the introduction of Genomic Unity® 2.0, we are the first lab to offer a whole genome sequencing test that includes both short and long reads. Extending the capabilities of traditional short-read sequencing, this cutting-edge technology provides an even more complete view of the genome, enabling even more diagnoses.
Intelligent analysis technology for rare genetic disorders across the lifespan
From small to large, simple or complex, we can accurately identify all major types of variants in your patient’s sample – variants other platforms and pipelines may miss. We analyze your patient’s genomic data from almost every angle using Genomic Intelligence®, our clinically validated whole genome platform. Designed and calibrated in-house, Genomic Intelligence® provides our experienced variant analysts capabilities to make striking diagnoses.
Sequence variant analysis
including single nucleotide variants, deletions/insertions, intronic, and regulatory variants
Short tandem repeat expansion analysis
in >44 genes
Structural & copy number variants analysis
including duplications, deletions, regions of homozygosity, mobile element insertions, inversions, and aneuploidy
Mitochondrial genome sequence analysis
with heteroplasmy and large deletions
Methylation pattern analysis
associated with Angelman, Prader-Willi and Fragile X syndromes
To learn more about the clinical performance of Genomic Intelligence®, see our publications
Precision oncology optimizes treatment & therapy management
Cancer requires action and action must be informed by knowledge. Understanding a cancer’s genomic landscape provides you vital information on treatment, management, and counseling strategies. To survey a cancer’s landscape, we use a suite of powerful genetic technologies – whole genome sequencing, exome sequencing, and targeted RNA analysis – so you and your patient have the best data to make the best decisions.
ClaudIA for Genomics®, our comprehensive data management platform, analyzes a patient’s genomic information using both the cancer and non-cancerous samples. Our concise report gives you and your patients actionable results for many cancers including drug resistance, drug effectiveness, prognosis, and more. This knowledge helps you build your patient’s precision therapy and management regimen on a strong foundation of data.
Services that simplify & support your practice
Our end-to-end services ensure you and your patients are supported throughout the genetic testing process. We coordinate with health insurance companies, communicate about costs, and can help collect samples. Our services help you focus on your patients, not the process.
Simplifying the health insurance billing process
Our hands-on approach lets you hand off insurance tasks to our experienced team members who perform benefits investigations, collect pertinent clinical information, and assess potential costs to avoid surprising bills. Expert genetics professionals review orders for clinical relevance, insurance guideline alignment, obtain letters of medical necessity, and support patients through the appeals process if a prior authorization is denied.
Patient & provider friendly
Starting a new testing service or replacing an existing one in your clinic can be a challenge. Our knowledgeable customer service team is available to support you and your patient at every step of the process from ordering, to sample collection, through results delivery. Our ordering process and online portal options streamline test ordering and results delivery. For patients, we meet them where they are, shipping kits to their homes or coordinating mobile phlebotomy services.
An expert touch
From our dedicated software engineers to our diligent variant scientists and lab directors, we have experts at every step of the testing and interpretation process. This leads to high quality and uniform results, for all of our tests.
Ready to learn more?
Connect with a Clinical Specialist to find out how easy it is to bring the power of whole genome sequencing to your practice.