SPRQ-Nx chemistry is now shipping worldwide, bringing sub-$300 HiFi genomes to the Revio platform!
This global rollout cuts sequencing costs by 30%, making it easier than ever to scale high-throughput workflows
Learn more: bit.ly/49HwmcL#PacBio#SPRQNx#Revio
Presenting our poster P23.040.D at #ESHG2026 today!
We're showcasing how #PureTarget and #PacBio HiFi sequencing enable flexible targeting of challenging genomic regions, from repeat expansions to difficult inherited disease genes.
Looking forward to the discussions! 😃
That is a wrap on our #ESHG2026 Corporate Satellite Symposium!
Thank you to everyone who joined us to learn how long-read population genomics is unlocking clinical impact, reducing testing complexity, and improving patient outcomes today. 🙌
#PacBio
Sharing results from a beta test of PacBio’s SPRQ-Nx reusable SMRT cells using two acquisitions!
This increased SMRT cell throughput reduces sequencing costs for large human WGS projects.
#ESHG2026#PacBio#ESHG
Next up, Adam Ameur shares that long-read WGS efforts are ongoing in Sweden for population genomics and clinical diagnostics.
They bridge these projects by using a joint analysis framework and shared variant databases.
#ESHG2026#PacBio#ESHG
The power of long-read sequencing lies not only in finding variants, but in understanding them.
Through phasing, it resolves complex alleles, determines the origin of de novo variants, and detects mosaicism—providing actionable insights that streamline diagnostics.
#ESHG2026
When standard methods fall short, long reads deliver.
Despite exome sequencing analysis, a genetic cause remained hidden. Long-read genome sequencing revealed a mobile element insertion in ADGRV1, solving this previously elusive case.
#ESHG2026#PacBio
Moving into accuracy: Not every detected variant is a true variant.
Lonneke shares a case where long-read genome sequencing revealed that an apparent LRP5 variant detected by short-read sequencing was actually just a sequencing artefact.
#ESHG2026#PacBio
Next up, Lonneke Haer Wigmans shares how long-read genome sequencing is becoming a diagnostic reality.
Before implementation, studies in 2023 and 2024 proved this novel technology is robust enough for clinical use and can replace existing testing methods.
#ESHG2026#PacBio
Big updates are coming for Vega in Q3 2026! Expect higher yield at 90 Gb per day and lower DNA input down to 500 ng.
Plus, you get flexible 2 to 24 hour run times, 5mC, 5hmC, and 6mA methylation calling, and 21 CFR part 11 support for audit tracking and instrument login control.
SPRQ-Nx on Revio is built for true walk-away simplicity.
SMRT Cells stay on the instrument and are entirely software managed. This automatic washing requires zero manual steps, leaving less time managing the instrument and more time on your science.
#ESHG2026#PacBio#SPRQNx
SPRQ-Nx is shipping now! 🚀
This brings complete genomes at a completely new price with automated multi-use SMRT Cells, upgraded performance up to 48 genomes/week, and richer 5hmC multiomic data.
#ESHG2026#PacBio#SPRQNx
We are live at our #ESHG2026 Corporate Satellite Symposium! 🧬
Stay tuned as we share updates on how long-read population genomics is unlocking clinical impact today by scaling research and transforming patient outcomes.
#PacBio
Coming up today at 10:30 in Hall C: Don't miss Session C15.1!
#PacBio Scientist Xiao Chen will showcase how HiFi sequencing resolves the complex D4Z4 repeat responsible for facioscapulohumeral muscular dystrophy. See you soon!
#ESHG2026
Day 1 at #ESHG2026 was incredible! Check out our Day 1 recap video to see what went down yesterday. 🎥👇
Onsite today? Don't forget to stop by our Corporate Satellite Symposium at 10:30 in Room A-5: "The power of long-read population genomics to unlock clinical impact."
Our Corporate Satellite Symposium starts in 1 hour at #ESHG2026!
⏰ 10:30-11:30
📍 Room A-5
🔬 The power of long-read population genomics to unlock clinical impact
Join #PacBio to see what's next.
Coming up today at 17:35 in Hall C: Don't miss Session PL3.4! 🧬
Discover how population-scale Kinnex long-read RNA sequencing of the 1000 Genomes Project is uncovering extensive novel isoform diversity. Join us!
#ESHG2026#PacBio#Kinnex
On my way to #ESHG2026 😃
If you're attending, stop by the #PacBio booth (420) to chat about #PureTarget and targeted HiFi sequencing.
Not in Göteborg? Check out this webinar recording below 👇
How can labs simplify analysis of repeat expansions and other complex genomic regions?
In this recorded webinar, Dr. Maximilian Thelen shares how he uses using PureTarget HiFi sequencing for repeat expansion analysis and custom panel development.
Watch: bit.ly/3S1axP5
PacBio is live at ESHG 2026! Stop by booth 420 to chat with our team, discuss your sequencing projects, and pick up some exclusive merch while supplies last.
Full conference agenda here: bit.ly/4nt9LWV#ESHG2026#HumanGenomics#PacBio
#PacBio has arrived in Gothenburg for #ESHG2026!🇸🇪
The team is on-site and ready to connect with the genetics community. We can't wait to discuss how HiFi sequencing is transforming clinical research pathways today.
Plan ahead with our full agenda: bit.ly/4nt9LWV
Are resolution limits holding back your research?
Join our live webinar to see how #PacBio HiFi sequencing delivers species- and strain-level clarity for human #microbiome workflows, followed by a live Q&A with Jeremy Wilkinson, PhD.
Register here: bit.ly/4nFgM6Z