WEBINAR: Catching the Unnoticed, What You’re Missing Matters
Published 2024-05-15
Our knowledge of the human genome is evolving and with it comes a deeper understanding of the pathogenetic of disorders. Nanopore comprehensive sequencing enables the interrogation of all forms of genomic variants and epigenetic in a single assay. This is already radically improving the landscape of reference genomes, leading to more complete and diverse references. This also is adopted in clinical settings for rare diseases, complex disorders and cancers providing new standards and expectations and richer insights. With the recently announced partnership, going from variant detection to interpretation is accessible to more use cases.
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