LAB SERVICES

NGS Analysis & Reporting
with Genomic Intelligence®

A CLINICALLY VALIDATED PLATFORM

Built to handle whole genome sequencing data, and everything else

We designed the Genomic Intelligence® platform to work with the most complex data available. As a result, it provides sample to clinical report integration and automation for genomic tests of any size or scale:

  • Probe- and amplicon-based gene tests
  • Multigene panels
  • Exome or whole genome
 PanelsExomeGenome
SNVs 
Small indels (<50bp) 

Structural variants
(≥50bp)

 
Mitochondrial variants (≥5% heteroplasmy) 
Tandem repeat expansions  

ROBUST VARIANT DETECTION, STREAMLINED VALIDATION

Proprietary algorithms detect all variant types

Developing a new clinical test requires a combination of secondary and tertiary validation exercises. As a clinical diagnostic lab that has processed tens of  thousands of samples, we have extensive expertise working with known positive and negative samples for calculation of sensitivity, specificity and positive predictive value for a wide variety of testing applications. Utilizing our expertise and unique library of samples significantly streamlines the validation process.

Ability to detect structural and mitochondrial variants depends on assay design, sequencing quality and sequencing depth

UNIQUELY FLEXIBLE CLINICAL REPORTING OPTIONS

Variantyx generated, signed clinical report

Ideal for labs new to NGS or for labs launching a test in a new clinical area, our board-certified clinical geneticists interpret the data, prepare and deliver a white-labeled, signed clinical report.

Variantyx generated, unsigned clinical report

For labs seeking an intermediate solution, our board-certified clinical geneticists interpret the data, prepare and deliver a white-labeled, unsigned clinical report for review and signature by your staff.

GENOMIC INTELLIGENCE® DELIVERS

High volume solutions

Seemless, end-to-end automation from sample to clinical report enables high volume processing of profitable tests

Fast time to launch

Leveraging our clinical expertise for assay validation, data interpretation and report sign off significantly reduces development time

Accurate test results

Our proprietary data analysis algorithms and sophisticated filters find complex variants missed by other analysis platforms