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Variant Interpretation in Oncology: Results From an End-User Benchmarking Survey
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"Variant Interpretation in Oncology: Results From an End-User Benchmarking Survey"

Conducted as a partnership between GenomeWeb and QIAGEN, the self-assessment survey aimed to understand how clinical NGS labs rate the current and desired state of their variant interpretation capabilities.

This report summarizes the results of a benchmarking survey that sought to identify pain points and opportunities in next-generation sequencing (NGS) variant interpretation workflows within the field of oncology.


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