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Celebrating 25 years of innovation
Join PacBio co-founder Jonas Korlach as he reflects on 25 years of scientific innovation—tracing the evolution of long-read sequencing and its transformative impact across genomics.
Human genomics
Promising clinical applications of long-read sequencing for genetic diseases
Aiping Mao, Director, Department of R&D, Berry Genomics Corporation
HiFi genomes help enable a first-tier generic test for all rare diseases
Alex Hoischen, Professor, Radboud University Medical Center
Exploring isoform diversity in the human brain using long-read RNA-sequencing
Christine Liu, Co-Founder & VP Data Analytics, Third Element Bio
Pioneering achievements of long-read sequencing for birth defects prevention
Desheng Liang, Professor, Center for Medical Genetics and Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University
One test fits all: the implementation of a clinical HiFi sequencing workflow for pediatric rare disease
Emily Farrow, Assistant Clinical Director, Clinical Genetics, Children’s Mercy Kansas City
Advantages of third-generation sequencing technology in the study and diagnosis of repeat expansions
Georgia Karadima, Associate Professor, Biology and Neurogenetics, National and Kapodistrian University of Athens
One year of HiFi sequencing at scale in Estonia
Lili Milani, Professor, Pharmacogenomics, University of Tartu
Decoding diversity: how HiFi sequencing is revolutionizing immune response and vaccine innovation
Melissa Smith, CEO, Clareo Biosciences, Inc.
Constitutive DNA hypermethylation of 45S ribosomal RNA genes in zebrafish
Michay Diez, PhD Candidate, Stowers Institute for Medical Research
High-quality pangenome construction enabled by HiFi reads
Mohammed Uddin, Director and Associate Professor, Center for Applied and Translational Genomics (CATG), MBRU, Dubai Health
Long reads for discovery and diagnoses
Niall Lennon, Chair and CSO, Broad Clinical Labs, Broad Institute of MIT and Harvard
Efficient long-read hybrid capture to resolve HLA haplotype variation
Omar Cornejo, Associate Professor, University of California Santa Cruz
PacBio Revio sequencing: a one stop shop for primary mitochondrial disease diagnostics
Robert Pitceathly, Professor, Clinical Neurology and Mitochondrial Medicine, University College London
The Chinese Pangenome Reference 2.0: Challenges and Solutions
Shuhua Xu, Professor, Shanghai Institute for Biological Sciences, Chinese Academy of Sciences
Implementing long-read HiFi sequencing: Amplicon, panel, and genome sequencing
Stuart Scott, Professor, Pathology; Director, Clinical Genomics, Stanford University – Stanford Health Care
Analytical validation of PacBio HiFi long-read sequencing to help support clinical decision making
Bhaven Mehta, Director – US NGS and Clinical Services, GENEWIZ from Azenta Life Sciences
