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:

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Technology backed by half a million genomic analyses on targeted panels and exomes
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Solutions tailored for each and every manufacturer and sequencing method
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A dedicated team of experts to support you all along the NGS workflow
A universal health data analytics platform for a decentralized approach to healthcare

Read More:

Focusing on what matters for rare and inherited diseases

Get the most out of your exome

Accelerating the assessment of germline variants

Accelerating the assessment of germline variants

Get the most out of your exome

Focusing on what matters for rare and inherited diseases

Webinars on-demand:

Robust CNV detection using whole exome sequencing for complex cases

Robust CNV detection using whole exome sequencing for complex cases

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Ensuring high resolution CNV detection

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Big panels, big challenges: CNV detection in WES

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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.