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Explore the PRISM 2026 video gallery—where global voices and visionary presentations
unveil the sequencing tools of tomorrow and the boundless possibilities of genomics.
Human Microbial + Plant-animal Cancer Sponsors
Human genomics
Target ALS data engine: an open data platform powering ALS research with HiFi sequencing
Amy Easton, VP, Scientific Programs, Target ALS and Evan Udine, Postdoctoral Fellow – Neuroscience, Mayo Clinic
Building Sweden’s long-read genome ecosystem
Anna Lindstrand, Professor, Karolinska Institutet
Improving our understanding of human genetic variation using long-read DNA and RNA sequencing
Danny E. Miller, Assistant Professor, University of Washington
HiFi sequencing: Helping to prevent misdiagnosis and missed diagnosis in rare disease
Emma Baple, Professor of Genomic Medicine, University of Exeter
HiHiFi genome sequencing of >4,000 infertile men – how human genetics can advance the development of novel non-hormonal contraceptives
Frank Tüttelmann, Director, Centrum für Medizinische Genetik, Klinik für Medizinische Genetik, Institut für Reproduktionsgenetik Universitätsklinikum Münster (UKM), Universität Münster
Population-scale Kinnex RNA sequencing of the 1000 Genomes Project reveals extensive novel regulatory and isoform diversity
Jonas (Gus) Gustafson, Graduate Student, University of Washington
Rare disease research in South Africa
Melissa Nel, Director, Clinical Omics and Informatics (COIN) Unit, Neuroscience Institute, University of Cape Town
Decoding Diversity with SMRT Sequencing to Deliver on the Promise of Precision Medicine
Melissa L. Smith, Chief Executive Officer, Clareo Biosciences
Genome-wide classification of tumor-derived reads from bulk long-read sequencing
Paul Spellman, Professor, UCLA
10,000 Estonian Biobank LR genomes for population-scale analysis of repetitive and complex genomic variants
Simone Rubinacci, EMBL Group Leader, Institute of Molecular Medicine Finland (FIMM), University of Helsinki
Implementing HiFi sequencing: Amplicon, panel, and genome sequencing
Stuart Scott, Professor in the Department of Pathology and Director of the Stanford Medicine Clinical Genomics Laboratory, Stanford
Towards long-read sequencing in rare disease diagnostics: early insights from a national study
Valtteri Wirta, Director Clinical Genomics, Science for Life Laboratory
Head of Department Clinical Genetics and Genomics, Karolinska University Hospital
Genomics across the lifespan: helping to transform rare disease care from diagnosis to prevention
Vorasuk Shotelersuk, MD, Director of the Center of Excellence for Medical Genomics, Chulalongkorn University, Thailand
Integrated assembly- and alignment-based long-read sequencing reveals novel genetic risk variants in autism spectrum disorder
Joon-Yong An, Associate Professor, Human Genomics, Korea University
Pediatric Rare Disease Genomics in India: Emerging Insights from Hackathon and Diagnostic Impact
Ashwin Dalal, Head, Diagnostics Division, Centre for DNA Fingerprinting and Diagnostics, Hyderabad
From Complexity to Clarity: Potential Clinical Impact of Long-Read Sequencing in Resolving Structural Variations
Usha Dutta, Diagnostics Division, Centre for DNA Fingerprinting and Diagnostics (CDFD)
From Cohort to Insight: Long-read Sequencing and Multi-omics in ToMMo
Kengo Kinoshita, Professor, Principal Deputy Executive Director, ToMMo Tohoku University
Vega sequencer for long read human genome sequencing: Technology Assessment and Practice
Yutaka Suzuki, Professor, Life Science Data Research Center (LISDAC), Graduate School of Frontier Sciences, the University of Tokyo
