What you’re not seeing can make a difference.
Get a robust and accurate assessment of CNVs
What you’re not seeing can make a difference.
Get a robust and accurate assessment of CNVs
SOPHiA GENETICS Offers:
Technology backed by half a million genomic analyses on targeted panels and exomes
Solutions tailored for each and every manufacturer and sequencing method
A dedicated team of experts to support you all along the NGS workflow
Read More:
Get the most out of your exome
Accelerating the assessment of germline variants
Focusing on what matters for rare and inherited diseases
Webinars on-demand:
Robust CNV detection using whole exome sequencing for complex cases
Ensuring high resolution CNV detection
Big panels, big challenges: CNV detection in WES
Learn more about our end-to-end, data-driven solutions or schedule a demo for SOPHiA DDM platform.
Our client services team is on hand to help.