Evaluation of a targeted RNA sequencing workflow for variant calling from FFPE samples in NSCLC

In the oncology field, many research laboratories are moving beyond just interrogating the genome for mutational analysis and seeking more dynamic biomarkers. RNA-based workflows paired with analytical solutions for molecular analysis of tumor-derived samples provide a deeper understanding of tumor biology in the context of non-small cell lung cancer (NSCLC). This application note has been done in collaboration with The medical center AZ Sint-Lucas (Ghent, Belgium).

Covered in this Application Note

RNA workflow accepts a broad range of sample input

RNA-Seq workflow capable of working with low sample input and enabling the sensitive discovery of expected and unexpected variants

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Genes

Oligo Pools

NGS Target Enrichment Solutions

Variant Libraries

Synthetic Controls

Antibody Discovery

Evaluation of a targeted RNA sequencing workflow for variant calling from FFPE samples in NSCLC

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