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Nanopore Sequencing: The Most Comprehensive Insight Into Cancer

The genetics behind cancer are both diverse and complex, with many abnormalities causing, contributing, or indicating the disease. Using nanopore sequencing, scientists can resolve variants and epigenetic modifications across the entire genome, target large panels or single genes, and detect known and novel full-length transcripts – for the most comprehensive insight into cancer genomes.

In this short, impactful video, scientists share how nanopore sequencing has made their work possible, leading to greater understanding of cancer, and how some of their own life experiences prompted them to pursue a career in this area.

Download this white paper to learn more about nanopore sequencing in cancer research

Read this case study on rapid, low-cost detection of genomic aberrations 


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