AMP 2025
Boston, MA
November 11-15, 2025
Thomas M. Menino Convention
and Exhibition Center
Booth #843
Join us at AMP 2025
Rethink what’s possible in human health and disease research.
Join us at AMP 2025 to discover how PacBio HiFi sequencing delivers the accuracy and completeness clinical and translational researchers need to see what others miss. Our long-read technology captures entire genes, resolves repeats, detects complex structural variants, and reveals phasing and methylation — all in a single workflow.
Stop by our booth #843 to chat with PacBio staff and have your questions answered and to see live demos of our Vega sequencing system.
We are excited to learn about your sequencing projects and research.
Booth hours:
November 13: 11:15 AM – 7:00 PM
(Welcome reception 6:00 – 7:00pm)
November 14: 9:00 AM – 4:00 PM
November 15: 9:00 AM – 1:30 PM
Meet with us
We’d love to hear what you’re working on.
Fill out the form and we’ll be in touch to schedule a meeting at the conference.
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INDUSTRY SPOTLIGHT
Presentation will be held on the Industry Spotlight Stage #1 on November 14, 2025 from 12:40pm – 1:10pm.
Discover how long-read HiFi sequencing is redefining what’s possible for clinical genomics and translational applications. In this workshop, we will highlight how labs and institutions are adopting HiFi targeted and whole genome sequencing to resolve challenging variants missed by conventional methods, including repeat expansions and complex structural variants. Learn about real-world examples spanning applications like oncology, neurology, and enabling carrier screening. Attendees will gain insight into how researchers are leveraging HiFi sequencing to help streamline genetic testing workflows, improve understanding of disease and treatment options, and support data interpretation and decision-making – delivering more complete, confident answers that may ultimately inform and advance patient care
PACBIO POSTER PRESENTATIONS
Poster presentations will be held in the exhibit hall.
POSTERS UTILIZING PACBIO SEQUENCING
Poster and oral presentations that feature PacBio sequencing.
Reimagining NGS Sample Prep:
End to End Automation for Faster Clinical Insights
CORPORATE WORKSHOP
TIME: Wednesday, November 12th from 3:00pm to 3:50pm EDT
LOCATION: Room 160C Level 1
Join Volta Labs for an inside look at how the Prinses Máxima Center is redefining pediatric cancer diagnostics through automation and innovation. Dr. Lennart Kester, Associate Group Leader and Clinical Molecular Biologist, will share how his team integrates Callisto’s fully automated sample preparation platform into cutting-edge clinical workflows for whole-genome sequencing using both long and short read platforms.
POSTER NO. G064
ABSTRACT NO.: 2169866
CATEGORY: GENETICS
TIME: Friday, November 14th from 9:15am-10:15am EDT
QIAseq xHYB Long Read Hereditary Cancer Panel targeted-capture accurately detects large structural variants through a streamlined workflow and straightforward analysis pipeline.
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. Copyright 2025. All rights reserved by Pacific Biosciences