Learn how sequencing solutions from Oxford Nanopore Technologies are transforming molecular pathology. Hear about the latest developments in nanopore sequencing which provide a comprehensive view of both conventionally sequenced single nucleotide variants and small indels, and the detection of structural, repetitive, copy number, and methylation variants ― all in a single sequencing run. With its ability to read any length of DNA or RNA, from short to ultra-long, come and learn how nanopore technology empowers you to answer the bigger and bolder research questions you have always wanted to ask.