McGill Genome Center

We've partnered with Oxford Nanopore since its earliest days, and that experience — backed by years of published research — means we know how to get the most out of your project. We provide end-to-end nanopore sequencing services, from DNA/RNA extraction and quality assessment through library preparation, flow cell loading, and basecalling with the latest algorithms. Our bioinformatics team supports downstream analysis including alignment, variant detection, and de novo genome assembly. We specialize in applications where Oxford Nanopore sequencing's strengths matter most, including long reads, structural variant detection, transcript analysis, and real-time applications like adaptive sampling for targeted enrichment.