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PacBio and DNAstack Launch First Global Federated HiFi Whole Genome Dataset to Accelerate Rare Disease Research

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PacBio (NASDAQ: PACB) and DNAstack launched the HiFi Solves Global Consortium to create the first global federated dataset of HiFi whole genome sequencing for rare disease research. The consortium spans nearly 30 institutions across 15 countries and has connected or committed to connect >b>10,000 HiFi whole genomes, enabling cross-border queries while data remain under local control.

The platform, hosted by DNAstack at hifisolves.org, supports secure federated queries, preserves data sovereignty, and leverages HiFi accuracy to improve detection of challenging variants and accelerate diagnoses for rare disease patients.

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Positive

  • Consortium size: nearly 30 institutions across 15 countries
  • Data scale: connected or committed to connect more than 10,000 HiFi whole genomes
  • Clinical validation: November 2025 study reported HiFi detected 100% of known variants in paralogous genes
  • Consortium growth: membership nearly doubled since 2023

Negative

  • Data status mix: figure includes genomes both connected and merely committed, not all datasets yet federated
  • No financial disclosure: announcement provides no revenue, commercialization terms, or guidance tied to the consortium

News Market Reaction – PACB

+5.06%
9 alerts
+5.06% News Effect
+2.1% Peak in 11 min
+$25M Valuation Impact
$513M Market Cap
0.1x Rel. Volume

On the day this news was published, PACB gained 5.06%, reflecting a notable positive market reaction. Argus tracked a peak move of +2.1% during that session. Our momentum scanner triggered 9 alerts that day, indicating moderate trading interest and price volatility. This price movement added approximately $25M to the company's valuation, bringing the market cap to $513M at that time.

Data tracked by StockTitan Argus on the day of publication.

Key Figures

Consortium institutions: nearly 30 institutions Participating countries: 15 countries HiFi genomes committed: more than 10,000 HiFi whole genome sequences +2 more
5 metrics
Consortium institutions nearly 30 institutions HiFi Solves Global Consortium membership
Participating countries 15 countries Geographic span of consortium members
HiFi genomes committed more than 10,000 HiFi whole genome sequences Federated dataset size for rare disease research
Variant detection rate 100% of known variants HiFi study on paralogous genes, November 2025
Consortium launch year 2023 Start of HiFi Solves Global Consortium

Market Reality Check

Price: $1.66 Vol: Volume 6,561,846 is sligh...
normal vol
$1.66 Last Close
Volume Volume 6,561,846 is slightly below the 20‑day average of 7,492,929 (relative volume 0.88). normal
Technical Shares at $1.58 are trading below the $1.62 200‑day moving average, reflecting a pressured longer‑term trend.

Peers on Argus

While PACB was down 1.86%, key peers like RXST (+2.19%) and SENS (+1.74%) were p...

While PACB was down 1.86%, key peers like RXST (+2.19%) and SENS (+1.74%) were positive, indicating stock‑specific dynamics rather than a sector‑wide move.

Historical Context

5 past events · Latest: Feb 18 (Neutral)
Pattern 5 events
Date Event Sentiment Move Catalyst
Feb 18 Conference participation Neutral +3.2% Management scheduled for TD Cowen health care conference fireside chat.
Feb 12 Earnings results Neutral +0.0% Reported Q4 and FY 2025 results with revenue growth and large GAAP loss.
Feb 12 Rare‑disease partnership Positive +0.0% Joined iHope network as first long‑read sequencing partner for rare diseases.
Feb 02 Asset sale Positive -8.8% Completed sale of short‑read assets to Illumina, receiving <b>$48.1M</b> net cash.
Jan 27 Earnings date set Neutral +2.0% Announced date and access details for Q4 and full‑year 2025 earnings call.
Pattern Detected

Operational and strategic updates, including asset sales and partnerships, have produced mixed price reactions, with some positive news coinciding with sell‑offs.

Recent Company History

Over recent months, PacBio has focused on long‑read sequencing and financial stabilization. It completed the sale of short‑read assets, generating about $48.1M in net cash and sharpening its strategic focus. Q4 and full‑year 2025 results showed revenue growth to $44.6M for Q4 and $160.0M for 2025, alongside a large GAAP net loss of $546.4M. The company also joined the iHope rare‑disease network and has maintained active investor engagement via conferences. Today’s global HiFi rare‑disease collaboration extends this strategy of partnering around long‑read technology.

Market Pulse Summary

The stock moved +5.1% in the session following this news. A strong positive reaction aligns with Pac...
Analysis

The stock moved +5.1% in the session following this news. A strong positive reaction aligns with PacBio’s strategy of expanding HiFi long‑read sequencing into global rare‑disease collaborations. The launch of a federated dataset exceeding 10,000 genomes across 15 countries builds on prior partnerships like iHope and recent asset divestitures focused on long‑read technology. Investors would still need to weigh ongoing GAAP losses and insider selling activity when assessing how durable any move might be.

Key Terms

hiFi whole genome sequencing, federated dataset, federated environment, paralogous genes, +2 more
6 terms
hiFi whole genome sequencing medical
"HiFi whole genome sequencing delivers the accuracy and completeness required..."
HiFi whole genome sequencing is a laboratory method that reads an individual’s entire DNA with long, highly accurate stretches rather than many short fragments, like scanning an entire book page by page instead of piecing together tiny scraps. For investors it matters because this higher accuracy and completeness can improve diagnostic certainty, reduce follow-up tests, and enable new clinical and research applications, which can translate into stronger demand, premium pricing, or competitive advantage for companies offering the service.
federated dataset technical
"the world’s first global federated dataset of HiFi whole genome sequencing data."
A federated dataset is a group of data sources that stay in their original locations but can be queried or analyzed together without moving or copying the raw data to a single place. Think of it like several libraries that keep their own books but share a common catalog so you can find and use information across all branches. For investors, this matters because it enables companies to build products and insights while reducing data-transfer costs, exposure to privacy or compliance risks, and barriers to partnerships—factors that can affect growth, legal risk, and competitive advantage.
federated environment technical
"within a highly secure federated environment."
A federated environment is a setup where multiple independent systems or organizations share access to data and services without moving or centralizing all their raw information, like neighbors who agree to share recipe summaries but keep their full cookbooks locked at home. Investors should care because this model can reduce legal and privacy risk, lower costs for scaling partnerships, and affect how quickly and securely a business can combine outside data to build products or make decisions.
paralogous genes medical
"clinically relevant variants in paralogous genes,” demonstrating the value..."
Paralogous genes are copies of a gene within the same organism that originated from a duplication event and often have similar DNA sequences but can evolve different roles over time. For investors, they matter because gene duplication can create redundancy or alternative biological pathways that affect how a drug works, change biomarker reliability, or introduce safety and regulatory uncertainty—think of them as duplicated tools in a toolbox that look alike but may perform different tasks.
structural variants medical
"including paralogous genes and structural variants, provide clinical researchers..."
Structural variants are large-scale changes in an organism’s DNA—such as missing, extra, flipped, or rearranged chunks of genetic material—that are like tearing out, duplicating, or reshuffling chapters in a book. Investors should care because these changes can drive or explain diseases, alter how well diagnostics and therapies work, and shift the commercial and regulatory outlook for drugs, tests, and gene-based treatments.
genome sequencing medical
"Genome sequencing can help deliver answers to patients who need it most —..."
Reading the full set of an organism’s DNA letters to reveal its genetic ‘instruction book.’ Think of it as scanning every page of a recipe or blueprint to see how something is built and how it might behave. For investors, genome sequencing matters because it powers diagnostic tests, drug development, and personalized treatments that can drive revenue, partnerships, regulatory scrutiny, and long‑term growth in biotech and healthcare companies.

AI-generated analysis. Not financial advice.

Collaboration powers secure international data sharing through the HiFi Solves Global Consortium

MENLO PARK, Calif., Feb. 24, 2026 (GLOBE NEWSWIRE) -- PacBio (NASDAQ: PACB), developer of the world’s most advanced sequencing technologies, today announced a collaboration with DNAstack to power the world’s first global federated dataset of HiFi whole genome sequencing data. Through the HiFi Solves Global Consortium, the collaboration enables secure international research — allowing genomic insights to travel across borders while sensitive data remains under institutional control.

Participating institutions connect HiFi whole genome sequencing data and associated metadata within a highly secure federated environment. Hosted by DNAstack and accessible at https://hifisolves.org, the platform enables researchers to query harmonized datasets across institutions without centralizing protected data, supporting global collaboration while maintaining compliance with regional data privacy regulations.

The consortium now includes nearly 30 clinical and research institutions across 15 countries spanning North America, Europe, the Middle East, Africa, East Asia, and Southeast Asia, with continued expansion underway. Collectively, members have connected or committed to connect more than 10,000 HiFi whole genome sequences — forming one of the largest and most diverse federated HiFi datasets dedicated to rare disease research.

“HiFi whole genome sequencing delivers the accuracy and completeness required to confidently detect even the most challenging variants,” said Christian Henry, President and Chief Executive Officer of PacBio. “By partnering with DNAstack, we are extending the power of HiFi sequencing beyond individual institutions — enabling secure, federated analysis at global scale while maintaining local data control. This combination of technological precision and international collaboration strengthens variant interpretation and accelerates discoveries for patients with rare disease.”

By increasing statistical power for rare disease studies, the federated model enables insights that would be much more difficult, if not impossible, within siloed datasets — while preserving data sovereignty and meeting regional compliance requirements.

“Genome sequencing can help deliver answers to patients who need it most — but only if we can learn from global datasets while protecting participants’ privacy,” said Marc Fiume, CEO at DNAstack. “This partnership is proving the value of securely connecting leading hospitals and research centers around the world without moving sensitive data. By enabling collaboration at this scale, we’re helping clinicians reach answers faster, improve rare disease diagnosis, and build the foundation for learning health systems that benefit entire populations.”

“For rare disease genomic analysis, accuracy and completeness are essential,” said Eric Vilain, M.D., Ph.D., UC Irvine School of Medicine and a member of the HiFi Solves Global Consortium. “Taking advantage of the consortium’s federated model, we can securely filter variants and interpret findings in the context of a diverse global dataset while maintaining full control of patient data — ultimately delivering clearer answers to families faster and with greater confidence.”

HiFi sequencing plays a central role in the consortium’s impact on better resolving the genetic underpinnings of rare diseases. Its high accuracy and ability to resolve complex genomic regions, including paralogous genes and structural variants, provide clinical researchers with greater confidence in detecting disease-causing variants. When combined with federated data sharing, HiFi sequencing enables interpretation of rare variants within a broader global context — improving confidence in understanding the biology of rare diseases and, ultimately, accelerating time to answers for patients and families.

In November 2025, consortium members from the EMEA region published the first major study from the HiFi Solves initiative, HiFi sequencing accurately identifies clinically relevant variants in paralogous genes,demonstrating the value of federated HiFi whole genome sequencing at scale. In the study, HiFi sequencing detected 100% of known variants, reducing the need for multiple complementary technologies and simplifying workflows.

Launched in 2023, the HiFi Solves Global Consortium brings together leading clinical genomics research organizations focused on advancing the use of highly accurate HiFi sequencing in rare disease research. Since its inception, the consortium has nearly doubled in size, reflecting growing global demand for collaborative, privacy-preserving genomic research models.

About PacBio

PacBio (NASDAQ: PACB) is a premier life science technology company that designs, develops, and manufactures advanced sequencing solutions to help scientists and clinical researchers resolve genetically complex problems. Our products and technologies, which include our HiFi long-read sequencing, address solutions across a broad set of research applications including human germline sequencing, plant and animal sciences, infectious disease and microbiology, oncology, and other emerging applications. For more information, please visit www.pacb.com and follow @PacBio.

PacBio products are provided for Research Use Only. Not for use in diagnostic procedures.

About DNAstack

DNAstack builds the trust infrastructure for biomedical data collaboration. Its federated platform connects genomic and clinical data across institutions, enabling researchers and clinicians to learn together while data stays under local control. DNAstack powers national and international precision health initiatives and is a global leader in open standards through the Global Alliance for Genomics & Health (GA4GH).

Forward-Looking Statements

This press release may contain “forward-looking statements” within the meaning of Section 21E of the Securities Exchange Act of 1934, as amended, and the U.S. Private Securities Litigation Reform Act of 1995. All statements other than statements of historical fact are forward-looking statements, including statements relating to the availability, uses, accuracy, advantages, quality or performance of, or benefits of using, or expected benefits of using, PacBio products or technologies, including in connection with the collaboration with DNA Stack and the HiFi Solves Global Consortium to, among other things, expand the range of genomic insights of participating consortia members, enable secure analysis of genomic data while meeting regional compliance requirements, deliver answers to, among others, clinical researchers and families, and provide greater confidence both in detecting disease-causing variants and understanding the biology of rare diseases, and the commitment to connect more than 10,000 HiFi whole genome sequences, among other future events. You should not place undue reliance on forward-looking statements because they are subject to assumptions, risks, and uncertainties and could cause actual outcomes and results to differ materially from currently anticipated results, including, challenges inherent in sequencing a large number of genomes and complying with evolving international privacy compliance requirements, the difficulty of generating discoveries in new areas of research or with respect to diseases that are rare; potential product performance and quality issues; rapidly changing technologies and extensive competition in, and potential FDA regulatory issues relating to, genomic sequencing; unanticipated increases in costs or expenses; interruptions or delays in the supply of components or materials for, or manufacturing of, PacBio products and products under development; third-party claims alleging infringement of patents and proprietary rights or seeking to invalidate PacBio's patents or proprietary rights, among others. Additional factors that could materially affect actual results can be found in PacBio's most recent filings with the Securities and Exchange Commission, including PacBio's most recent reports on Forms 8-K, 10-K, and 10-Q, and include those listed under the caption "Risk Factors." These forward-looking statements are based on current expectations and speak only as of the date hereof; except as required by law, PacBio disclaims any obligation to revise or update these forward-looking statements to reflect events or circumstances in the future, even if new information becomes available.

Contacts

Investors:
ir@pacb.com

Media:
pr@pacb.com


FAQ

What did PacBio (PACB) and DNAstack announce on February 24, 2026 about HiFi whole genome data?

They launched the HiFi Solves Global Consortium to federate HiFi whole genome datasets across institutions. According to PacBio, the consortium connects nearly 30 institutions in 15 countries and has connected or committed to connect over 10,000 HiFi genomes for rare disease research.

How does the HiFi Solves Global Consortium preserve patient privacy while enabling global research?

The consortium uses a federated model so genomic data remain under local control while queries travel across sites. According to PacBio, DNAstack hosts a secure platform that lets researchers query harmonized metadata without centralizing protected data.

How many HiFi whole genomes are included in PacBio's (PACB) federated dataset as of February 24, 2026?

Members have connected or committed to connect more than 10,000 HiFi whole genomes. According to PacBio, that total combines datasets already linked and those committed for future federation across participating institutions.

What evidence supports HiFi sequencing accuracy cited by PacBio (PACB) in the consortium announcement?

A November 2025 consortium study found HiFi sequencing detected 100% of known variants in paralogous genes. According to PacBio, this result reduced the need for multiple complementary technologies and simplified clinical workflows.

Which regions and how many institutions participate in the HiFi Solves Global Consortium mentioned by PacBio (PACB)?

The consortium includes nearly 30 clinical and research institutions across 15 countries in North America, Europe, Middle East, Africa, East Asia, and Southeast Asia. According to PacBio, expansion is ongoing with additional members joining.

What immediate benefits does PacBio (PACB) claim the HiFi federation provides for rare disease diagnosis?

The federation increases statistical power and enables interpretation of rare variants in a global context while preserving data sovereignty. According to PacBio, this helps clinicians reach answers faster and improves confidence in variant interpretation for families.
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