This webinar discusses the critical role of genomic interpretation software for clinical labs looking to establish comprehensive NGS testing programs. Accurate and fast software for variant calling, alignment, interpretation, and clinical reporting is an essential component of genomic medicine, with the potential to significantly impact patient outcomes and improve healthcare economics.
September 28, 2017
Sponsored by
Fabric Genomics
Clinical Utility of Comprehensive and Fast Genomic Interpretation
Genome Webinar
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