Dr. Hagen Tilgner: Based at Weill Cornell Medicine, Tilgner’s work focuses on leveraging ultra-long-read sequencing technologies, notably from Oxford Nanopore, to decode intricate transcriptomic landscapes, advancing our understanding of complex RNA molecules.
Prof. Mark Akeson: A pioneer at UC Santa Cruz, Akeson’s research has been foundational in the development of nanopore-based sequencing technologies, which are at the heart of ultra-long-read sequencing approaches.
Dr. Nick Loman: As a professor at the University of Birmingham, Loman is known for his contributions to genome sequencing using Oxford Nanopore Technologies. His real-time sequencing of bacterial genomes provides vital insights into pathogen transmission and resistance.
Dr. Eoghan Harrington: Operating out of the Earlham Institute, Harrington’s work emphasizes the application of ultra-long-read sequencing in plant genomes, facilitating deeper understanding and innovation in crop sciences.
Dr. Karen Miga: Working at UC Santa Cruz, Miga’s research on completing human genome sequences using ultra-long reads has filled gaps left by traditional short-read sequencing methods.
Prof. Han Cao: Founder of BioNano Genomics, Cao’s expertise lies in optical genome mapping, an approach that complements ultra-long-read sequencing, enabling more comprehensive genomic studies.
Dr. Can Alkan: At Bilkent University, Alkan’s focus is on computational genomics. His contributions enhance the algorithms and tools used in processing and understanding data from ultra-long-read sequencing platforms.
Dr. Jared Simpson: Based at the Ontario Institute for Cancer Research, Simpson has been instrumental in developing software solutions for nanopore sequencing data, such as the renowned nanopolish.
Prof. Michael Schatz: At Johns Hopkins University, Schatz’s work in computational biology includes improving the assembly and validation of ultra-long-read sequencing data, addressing challenges in the field.
Dr. Winston Timp: Also at Johns Hopkins University, Timp’s research bridges the gap between nanopore sequencing technologies and practical applications in genomics, enhancing both precision and accessibility.
