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PacBio Joins iHope Initiative as First Long-Read Genomic Sequencing Partner

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PacBio (NASDAQ: PACB) is joining the iHope global rare-disease genomics network as its first long-read sequencing partner to integrate HiFi long-read whole-genome sequencing.

iHope supports more than 1,000 patients annually across 25 clinical sites in 14 countries. Integration is expected to begin in early 2026 and aims to improve detection of challenging variants and support future precision-therapeutic research.

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Positive

  • HiFi WGS integration into iHope network
  • Network reach: 1,000+ patients annually across 25 sites, 14 countries
  • Expected start of integration in early 2026
  • Supports research into antisense oligonucleotide therapeutic approaches

Negative

  • None.

Key Figures

Patients supported annually: more than 1,000 patients Clinical sites: 25 clinical sites Countries covered: 14 countries +1 more
4 metrics
Patients supported annually more than 1,000 patients Scale of iHope rare-disease genomic testing network
Clinical sites 25 clinical sites Global footprint of iHope network
Countries covered 14 countries Geographic reach of iHope network
Integration timing early 2026 Expected start of PacBio HiFi integration into iHope

Market Reality Check

Price: $1.84 Vol: Volume 6,146,770 vs 20-da...
normal vol
$1.84 Last Close
Volume Volume 6,146,770 vs 20-day average 7,954,118, indicating lighter-than-normal trading activity. normal
Technical Price $1.84 trades above 200-day MA at $1.60, yet remains 32.6% below the 52-week high of $2.73 and 116.19% above the 52-week low of $0.8511.

Peers on Argus

PACB is up 1.66% while key peers show mixed to negative moves: DCTH -5.94%, RXST...

PACB is up 1.66% while key peers show mixed to negative moves: DCTH -5.94%, RXST -2.37%, SENS -7.23%, with modest gains in SRDX +0.26% and CTKB +0.57%. No peers appeared in the momentum scanner and no same-day peer headlines were flagged, pointing to a stock-specific reaction.

Historical Context

5 past events · Latest: Feb 02 (Positive)
Pattern 5 events
Date Event Sentiment Move Catalyst
Feb 02 Asset sale & refocus Positive -8.8% Completed sale of short-read assets to Illumina, sharpening long-read focus.
Jan 27 Earnings date set Neutral +2.0% Announced timing of Q4 and full-year 2025 earnings call and webcast.
Jan 12 Rare disease collab Positive +3.6% Planned collaboration with n-Lorem and EspeRare using HiFi long-read WGS.
Jan 12 Clinical adoption news Positive +3.6% HiFi WGS adopted as first-line approach in SUDC study of 200 families.
Jan 12 Prelim revenue update Positive +3.6% Reported Q4 2025 revenue of $44.6M and full-year $160.0M with YoY growth.
Pattern Detected

Recent positive strategic and clinical updates (rare disease collaborations, preliminary revenue growth) most often coincided with positive price reactions, while the short-read asset sale saw a negative reaction despite balance sheet benefits.

Recent Company History

Over the last few months, PACB has emphasized a pivot toward long-read sequencing and rare disease applications. On Jan 12, 2026, it reported preliminary $44.6M Q4 and $160.0M 2025 revenue alongside rare disease collaborations, with shares rising around 3.6%. The Feb 2, 2026 sale of short-read assets brought about $48.1M in net cash but led to an 8.85% decline. Today’s iHope partnership continues the rare-disease, long-read focus seen in January collaborations.

Market Pulse Summary

This announcement deepens PACB’s role in rare-disease genomics by adding HiFi long-read whole-genome...
Analysis

This announcement deepens PACB’s role in rare-disease genomics by adding HiFi long-read whole-genome sequencing to iHope’s network, which supports over 1,000 patients annually across 25 sites in 14 countries. It extends a recent series of rare-disease collaborations and builds on January’s preliminary revenue update. Investors may watch how quickly integration begins in early 2026, the scale of sample volumes, and how these partnerships translate into sustainable instrument and consumables demand.

Key Terms

whole-genome sequencing, long-read sequencing, antisense oligonucleotide–based, precision care
4 terms
whole-genome sequencing medical
"HiFi Long-Read Whole-Genome Sequencing Expands the Collective Capabilities..."
Whole-genome sequencing is the process of reading an organism’s entire DNA instruction manual to capture all genetic information rather than just selected parts. For investors, it matters because having the full genetic picture can reveal new diagnostics, drug targets, or personalized treatments that drive product value, regulatory approvals, and long-term revenue potential, while improvements in speed and cost can expand market reach like making a complex map easier and cheaper to produce.
long-read sequencing medical
"PacBio (NASDAQ: PACB), a leading provider of high-quality, long-read sequencing technologies..."
Long-read sequencing is a laboratory method that reads much longer stretches of DNA at once than older approaches, giving a clearer, more continuous picture of a genome—like reading whole sentences instead of just chopped-up words. For investors, it matters because it can improve accuracy of genetic tests, speed up drug research, reduce costly follow-up testing, and create competitive advantages for companies that develop or use the technology in diagnostics and therapeutics.
antisense oligonucleotide–based medical
"support future research into precision therapeutic approaches, including antisense oligonucleotide–based strategies."
A therapy approach using short, synthetic strands of genetic material designed to stick to a cell’s messenger RNA — the copy of a gene’s instructions — and block or change those instructions so a faulty or harmful protein isn’t made. Investors care because these treatments offer highly targeted ways to treat specific genetic conditions, which can mean big potential rewards but also high development costs, clinical risk, and manufacturing and regulatory complexity.
precision care medical
"may help support its delivery of precision care."
Precision care is healthcare tailored to an individual’s unique biology, lifestyle and test results so treatments and prevention are chosen to work best for that specific person rather than using one-size-fits-all approaches. For investors, it matters because targeted therapies and diagnostics can raise the chance of successful outcomes, reduce wasted spending, enable premium pricing and create niche markets — think of a tailored suit versus off-the-rack clothing, where better fit can command higher value and loyalty.

AI-generated analysis. Not financial advice.

Integration of HiFi Long-Read Whole-Genome Sequencing Expands the Collective Capabilities of iHope’s Global Rare Disease Network

MENLO PARK, Calif., Feb. 12, 2026 (GLOBE NEWSWIRE) -- PacBio (NASDAQ: PACB), a leading provider of high-quality, long-read sequencing technologies, today announced a collaboration with iHope, a global rare disease genomics program of Genetic Alliance, to integrate PacBio’s HiFi® long-read whole-genome sequencing into iHope’s international network.

iHope operates the world’s largest equitable rare-disease genomic testing network, supporting more than 1,000 patients annually through 25 clinical sites across 14 countries. The program is designed to enable collaborative, multi-technology support for rare disease patients, bringing together diverse approaches and clinical expertise to address the biological complexity of rare genetic disorders. The addition of PacBio’s HiFi long-read whole-genome sequencing aims to expand the range of genomic insights available across the network, providing data that supports iHope’s mission to ultimately drive more diagnostic clarity.

“We've been impressed with the progress iHope has made in getting answers for rare disease patients through the use of genomics and we believe HiFi Long-Read WGS can move the needle even more by finding variants that may have been otherwise missed,” said Christian Henry, President and Chief Executive Officer, PacBio. “HiFi long-read sequencing offers a complete view of the genome, and through this collaboration we aim to help expand iHope’s access to more comprehensive and advanced genomic research technologies that may help support its delivery of precision care. As February is Rare Disease Month, we’re reminded that every patient matters and we’re proud to support iHope’s efforts to help bring clarity and hope.”

By integrating PacBio long-read sequencing alongside diagnostic approaches, iHope will strengthen its ability to interrogate challenging regions of the genome and explore additional classes of genetic variation. PacBio and iHope aim to broaden opportunities for patients with unresolved findings, while reinforcing a shared learning environment in which advances at one laboratory or clinical site can inform and elevate care across the entire network. The PacBio - iHope collaboration is designed to support future research into precision therapeutic approaches, including antisense oligonucleotide–based strategies.

“We are delighted to welcome PacBio to the iHope network. This collaboration will further advance our mission to deliver diagnoses to families who have historically lacked access to advanced genomic tools,” said Ryan J. Taft, Chief Scientific Officer, Genetic Alliance. “Our experience shows that access to advanced genomic technologies, like PacBio’s long-read genomes, can profoundly and positively impact patient lives across diverse populations and geographies.”

Integration of PacBio HiFi sequencing into the iHope network is expected to begin in early 2026.

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 Genetic Alliance

Genetic Alliance is a nonprofit health advocacy organization founded in 1986 to improve health through genetics and genomics. With a global network of thousands of disease-specific organizations, research institutions, clinicians, and industry partners, Genetic Alliance works to ensure that individuals and families—especially those affected by genetic and rare conditions—have access to accurate information, appropriate care, and meaningful participation in research.

iHope is a flagship program of Genetic Alliance that provides no-cost clinical genome and exome sequencing for children with suspected genetic conditions who lack access to testing due to geography or resources. iHope was launched by Illumina, Inc, Founding Partner and current Platinum Sponsor of iHope, and builds on Illumina’s clinical sequencing expertise. The program is designed to be scalable, ethical, patient-first and focused on individuals with limited access to genomic medicine. Through a global network of partner laboratories and clinical sites, iHope prioritizes diagnosing the undiagnosed, supporting families after results are returned, and empowering participants with control over their own genomic data. 

For more information, visit www.geneticalliance.org.

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 iHope collaboration to, among other things, expand the range of genomic insights across its network, drive diagnostic clarity, interrogate challenging regions of the genome, explore additional classes of genetic variation and find variants that may otherwise be missed, support its delivery of precision care and expand its access to more comprehensive genomic sequencing technologies, broaden opportunities for patients with unresolved findings, and support research into precision therapeutic approaches; expectations with respect to the timing to integrate PacBio HiFi sequencing into the iHope network; and 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, the difficulty of generating discoveries in new areas of research; 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 announce about joining iHope on February 12, 2026 (PACB)?

PacBio announced it will integrate HiFi long-read whole-genome sequencing into iHope's network. According to the company, the integration aims to expand genomic insights for rare-disease patients across iHope sites.

How many patients and sites will benefit from PacBio HiFi integration in the iHope network (PACB)?

The collaboration covers iHope's network supporting more than 1,000 patients annually across 25 clinical sites in 14 countries. According to the company, this will broaden access to long-read sequencing globally.

When will PacBio's HiFi sequencing be integrated into iHope (PACB)?

Integration is expected to begin in early 2026. According to the company, rollout will add long-read capabilities alongside existing diagnostic approaches across the iHope network.

What diagnostic benefits does PacBio HiFi long-read WGS bring to iHope patients (PACB)?

HiFi long-read WGS can detect complex and previously missed variants in challenging genome regions. According to the company, this aims to improve diagnostic clarity for unresolved rare-disease cases.

Will the PacBio–iHope collaboration support therapeutic research (PACB)?

Yes. The collaboration is designed to support future research into precision therapeutics, including antisense oligonucleotide strategies. According to the company, sequencing data will inform translational research across the network.
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