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Accurate and Reproducible Detection of Fusions and Exon Skipping Events in NSCLC-Derived Samples Using A Comprehensive, Targeted RNA-Seq System Across Multiple Laboratories
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"Accurate and Reproducible Detection of Fusions and Exon Skipping Events in NSCLC-Derived Samples Using A Comprehensive, Targeted RNA-Seq System Across Multiple Laboratories"

Increasingly, RNA-associated variants are being recognized as clinically relevant within the analysis of non-small cell lung cancer specimens

Rather than conducting individual, sequential tests to identify these variants, RNA-seq enables the massively parallel sequencing of samples to detect these variants in a single run from a small specimen. This poster describes how the QuantideX NGS RNA Lung Cancer Kit enables the highly sensitive, specific, and reproducible detection of RNA fusions and exon-skipping events from precious FFPE tumor specimens.

The QuantideX NGS RNA Lung Cancer Kit is for research use only.


Offered Free by: Asuragen
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