Big updates coming to Vega!
SPRQ-Nx chemistry drops cost per Gb by 40% with 90 Gb yield, $995 run pricing, 500 ng input minimums, 2-to-4 hour run times, and 21 CFR Part 11 compliance controls.
Read the press release to explore the full specs: https://t.co/3yguv6Qd93
How does Illumina TruPath compare with PacBio HiFi WGS?
Using publicly available HG002 benchmark data, this post compares several examples of read support, variant calling, phasing, methylation, and the use of pangenome references for each approach.
🔗👇 https://t.co/LW0WvrT3Ok
What can you learn from a clinical lab's PureTarget implementation?
Discover how CHU Nîmes in France implemented PacBio PureTarget and transitioned to routine clinical use in just ~3 months to expand their repeat expansion testing.
Read the story: https://t.co/hJKRDjFnCz
Last call! Register for our New Technology Session: HiFi Long-Read Bioinformatics Bootcamp.
Learn to turn raw data into insights, master file formats and workflows for genomes or transcriptomes, and get on-demand lessons plus live Q&A access.
Register: https://t.co/EOgWpsujwW
Supercharge your sequencing lab with Vega and SPRQ-Nx chemistry! ✨
Experience higher yield, lower DNA input, and fast run times.
Whether you work in biopharma, clinical targeted, or microbial genomics, explore our 3 HiFi Playbooks and download yours: https://t.co/meSmPfIGpE
De novo variant discovery in 44% of unresolved cases, T2T pangenomes, and single-molecule epigenomics.
See how HiFi sequencing is redefining precision medicine from the keynotes at APAC PRISM 2026 in Fukuoka.
Read the recap and watch on demand. 👇https://t.co/pXSP2x9OlW
Find your HiFi Fit Kit in under a minute: https://t.co/Iz0v0vCsLc
Not every sequencing project starts in the same place.
Answer 3 quick questions about your specific research goals, and we'll match you to a personalized resource bundle for your work in ~45 seconds.
Get the complimentary Rapid HiFi WGS Resource Bundle for immediate access to our technical note, ESHG poster, and pipeline application notes.
Learn how to go from DNA to genome-wide variant calls in under 30 hours and capture complex structural variants: https://t.co/3p4GMBqFGg
When does long-range PCR make sense for targeted HiFi sequencing?
If your target amplifies cleanly, LR-PCR is a simple and cost-effective option.
Read our new blog to see exactly where it fits in targeted workflows and get practical assay design tips.👇https://t.co/TBTP7px2mk
Register for our upcoming webinar on long-read multiomics for human disease research!
Hear three leading experts share how integrating genomics, transcriptomics, and proteogenomics advances rare disease and biopharma discovery.
Save your spot today: https://t.co/JzMdBdUc0w
Back by popular demand! Access one of our most-watched sessions on solving rare disease cases with HiFi sequencing.
Get expert real-world cohort stories plus instant bonus access to our newest white paper on solve rates.
Watch & download the whitepaper: https://t.co/bSDDlqFoM8
Skip the spec sheet deep dives! Find your optimal sequencing setup in under a minute: https://t.co/Iz0v0vCsLc 🧬
Answer 3 quick questions about your research goals to unlock custom application guidance & real-world use cases matched directly to your work.
#PacBio
Last call! Our webinar is tomorrow.
Registration is still open to learn how SPRQ-Nx chemistry on Vega drives performance up and costs down. See how lower DNA input, higher HiFi yield, and 21 CFR Part 11 support accelerate your workflows.
Register here: https://t.co/L5wYbzFK2Y
The omics technologies shaping biology today probably aren’t in your graduate textbook…yet.
Combining genomes, spatial biology, microbiomes, and more reveals biology invisible to any single assay. Read our Essential Guide to Modern Multiomics.
Download: https://t.co/uUWLy9s1cV
Congrats to Yanding Zhao, winner of the 2026 SMRT Grant for long-read cancer multiomics! 🏆🧬
Yanding is leveraging #PacBio HiFi sequencing to uncover non-canonical HRD mechanisms and structural variants in high-risk osteosarcoma.
Read more: https://t.co/z7tsEXmrUW
Join our New Tech Session: HiFi Long-Read Bioinformatics Bootcamp! 🧬
Build a solid foundation for analyzing #PacBio HiFi data with an on-demand video playlist plus a live Q&A with PacBio experts. Learn core tools & best practices.
Register today: https://t.co/EOgWpsujwW
One of our most-requested #RareDisease sessions is available for a limited time!
Learn how HiFi sequencing boosts solve rates in undiagnosed cohorts.
Sign up today for instant access to the session + a direct download of our latest white paper: https://t.co/bSDDlqFoM8
Choosing the right targeted sequencing workflow shouldn't be hard.
From repeat expansions to large genomic regions, different applications need different approaches.
Our Targeted 101 series helps you find the right fit. Sign up for expert resources: https://t.co/scmmKNfwfE
Registration is still open for our webinar on how SPRQ-Nx chemistry on Vega drives performance up and costs down. Learn how lower DNA input, higher HiFi yield, and 21 CFR Part 11 support accelerate your workflows.
Register here: https://t.co/L5wYbzFK2Y
#PacBio#Vega#SPRQNx
Find your optimal sequencing strategy in under a minute.
Answer 3 quick questions about your research to get matched with a personalized #PacBio HiFi Fit Kit tailored to your goals.
Take the 45-second quiz for instant access: https://t.co/Iz0v0vD0AK