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Clinical Interpretation and Reporting.

In the world of oncology and inherited disease, every case may be influenced by unseen complexities in the patient’s unique genetic makeup. As genomic science makes incredible strides in capturing and documenting genomic data, we are here to seamlessly integrate these cutting-edge findings into your lab’s clinical interpretation and reporting workflows. 

At Velsera, we elevate confidence in your lab’s diagnostic and treatment decisions with a suite of interpretation and reporting tools built specifically for precision medicine powered by an unmatched library of expert-curated clinical data. By connecting and visualizing clinical and research knowledge from around the world, we are your partners in the mission to succeed in delivering the most effective treatments for patients in urgent need of answers. 

Solutions

Clinical Genomics WorkSpace

Streamline sequencing-based clinical tests with a genomic analysis and reporting platform powered by data science and informed by an expansive and exclusive data-sharing network of clinical grade information.
Streamline sequencing-based clinical tests with a genomic analysis and reporting platform powered by data science and informed by an expansive and exc...

Knowledgebase

Reach a world of indispensable knowledge where advanced machine learning, combined with expert curation and review, delivers the information you need to unlock your next insight right in your workspace. Automate the knowledge-gathering and citation in your reporting process with ...
Reach a world of indispensable knowledge where advanced machine learning, combined with expert curation and review, delivers the information you need ...

Reporting and Sign Out Support

Access board-certified medical directors to oversee variant analyst services and support sign-out of clinical reports.
Access board-certified medical directors to oversee variant analyst services and support sign-out of clinical reports.