ASHG 2025
Boston, MA
October 14-18, 2025
Booth #919
Join us at ASHG 2025
Stop by our booth #919 to connect with PacBio scientists and staff, see live demos of our Revio and Vega sequencing systems, and learn how our long-read technology is advancing human genomics — from rare disease research to population-scale studies. Enter our daily drawing to win a Labubu, and don’t forget to sign up for the ASHG Party — it’s going to be unforgettable!
Booth hours:
October 15: 9:30 AM – 4:30 PM
October 16: 9:30 AM – 4:30 PM
October 17: 9:30 AM – 4:30 PM
Meet with us
We’d love to hear what you’re working on.
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25 years of discovery: Building the future of genomics together
Friday, October 17 | 12:00pm – 1:00pm ET
Room 153ABC, Level 1
For 25 years, our knowledge of genomics has grown through innovation and collaboration, driving breakthroughs and discoveries that once seemed impossible. This workshop will celebrate the power of collaboration and shared knowledge in advancing human genomics. We’ll explore how HiFi sequencing is enabling new insights into complex biology and disease, empowering large-scale studies that connect researchers worldwide. Attendees will also hear about the latest updates and innovations in PacBio technology, designed to help the community do more with every run. Join us to reflect on the journey so far and discover how working together will shape the next era of genomics innovation.
This workshop is an opportunity to connect with peers, exchange ideas with experts, and explore how HiFi sequencing can be applied in your own research. A complimentary box lunch will be provided while supplies last.
CoLab 1
Wednesday
October 15th
3:15pm – 3:45pm ET
CoLab Theater 1
HiFi sequencing at scale: Targeted native DNA sequencing with PureTarget
This session will showcase PacBio’s updated PCR-free PureTarget products for sequencing of the most challenging genes. Hear from customers applying off-the-shelf panels for high throughput human germline diagnostic research and custom panels for disease research on engineered cell lines.
CoLab 2
Thursday
October 16th
2:30pm – 3:00pm ET
CoLab Theater 2
Beyond DNA: Connecting Genomes, Transcriptomes, and Proteomes with HiFi Sequencing
Understanding biology requires more than DNA sequence alone. This CoLab will demonstrate how multiomic applications with HiFi sequencing, from full-length isoform detection to integrated proteogenomics, are advancing knowledge of human cell types and disease pathways. Learn how long-read multiomics provides a more comprehensive view of biology, revealing connections between genetic variation, isoforms, and protein diversity.
CoLab 3
Friday
October 17th
10:15am – 10:45am ET
CoLab Theater 1
New frontiers: Expanding the capabilities of HiFi sequencing with cutting-edge technology updates
PacBio technology continues to evolve, helping researchers gain more insight from each sample.
This session will feature: 1) advances in long-read epigenomics using Fiber-seq from EpiCypher to provide integrated chromatin accessibility, genome, and methylome information from a single WGS library and sequencing run, and 2) workflow and platform updates on Revio that improve efficiency, scalability, and cost. Join us to see how emerging technologies are reshaping the future of long-read sequencing and genomics research.
PLATFORM TALK + POSTER PRESENTATION SESSIONS
Platform talk will be held in Room 253ABC/Level 2. Poster presentations will be held October 15-17 in the exhibit hall.
PLATFORM TALK
Computational analysis of tandem repeats for genome-wide identification of novel repeat expansions
Thursday, October 16 | 1:30-2:30pm ET
Session 54 – Function of Complex Variation and Repeats
Room 253ABC/Level 2
Thomas Michael Menino Convention & Exhibition Center
Presenter: Egor Dolzhenko
POSTERS UTILIZING PACBIO SEQUENCING
Poster 4071F
Benchmarking long-read variant sensitivity across ONT and PacBio platforms using known clinically reported variants in a cohort of critically ill newborns
University of Washington
Poster 7050W
The impact of structural variants on rare disease diagnosis from short and long read sequencing
The Broad
Platform talk
Leveraging long-read sequencing to identify de novo variants from parent-proband duos
UC Irvine, Children’s National, GREGoR
Poster 6029F
Long-read RNA sequencing of 1000 Genomes Project cell lines provides a high-resolution view of transcriptomic variation across diverse human populations
John Hopkins University (on behalf of 1KGP LRS Consortium
Platform talk
Resolving genome regulatory complexity with new multiomic long-read sequencing tools for chromatin state, DNA methylation, and genetic variation
Epicypher
Poster 5038F
QIAseq xHYB long read HLA capture: An accurate, user friendly, scalable long read solution for class I and class II HLA haplotyping
Qiagen
Poster 9025T
A streamlined library prep workflow with Comprehensive Genome Profiling (CGP) panel, and PacBio long-read sequencing, provide a holistic view of tumor biology
Agilent
Poster 4008W
Highly multiplexed custom CRISPR sequencing with PacBio PureTarget assay for detecting genome editing alterations
University of Michigan
Research use only. Not for use in diagnostic procedures. © 2025 Pacific Biosciences of California, Inc. (“PacBio”). All rights reserved. Information in this document is subject to change without notice. PacBio assumes no responsibility for any errors or omissions in this document. Certain notices, terms, conditions and/or use restrictions may pertain to your use of PacBio products and/or third-party products. Refer to the applicable PacBio terms and conditions of sale and to the applicable license terms at pacb.com/license. Pacific Biosciences, the PacBio logo, PacBio, Circulomics, Omniome, SMRT, SMRTbell, Iso-Seq, Sequel, Nanobind, SBB, Revio, Onso, Apton, Kinnex, PureTarget, SPRQ, and Vega are trademarks of PacBio.
