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\nThe Use of Amplified and Synthetic ctDNA to Assess Variant Calls from Targeted NGS Panels\n
In this poster video from SeraCare, learn how to evaluate variant calls generated by targeted sequencing NGS panels using different highly multiplexed ctDNA reference materials that contain INDELs, indels, structural variants, and CNVs at various allele frequencies.
\nAvailable here.\n

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