Advancing carrier screening and diagnostic applications research with long-read sequencing

In this on-demand webinar, explore how the AmplideX® Nanopore Carrier Plus Kit, formed by combination of the Asuragen Carrier Screening kit and Oxford Nanopore sequencing, supports comprehensive carrier screening in a streamlined workflow. Designed to assess 11 genes associated with high at-risk couple rates, this approach enables simultaneous detection of SNVs, indels, CNVs, STRs, and structural variants in a single assay.

Discover how nanopore sequencing provides detailed resolution of complex genomic regions—including AGG interruptions in FMR1, structural variation in CYP21A2/TNXB, and copy number differentiation of SMN1/SMN2—while leveraging key Oxford Nanopore features such as real-time data generation, scalable throughput, and rich sequence context to simplify analysis and enhance insight.

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