PacBio (NASDAQ: PACB), a leading developer of high-quality, highly
accurate sequencing solutions, announced that Precision Health
Research, Singapore (PRECISE) has chosen the Revio HiFi sequencing
system for its Long-Read Sequencing Flagship Project. This
initiative aims to generate the largest long-read sequencing
dataset in Southeast Asia, marking a significant advancement for
precision medicine in Singapore.
As part of Singapore’s three-phase National Precision Medicine
(NPM) programme, the current phase of the NPM aims to transform
healthcare in Singapore and improve patient outcomes through new
insights into the Asian genome. Hence, this collaboration will
harness PacBio's state-of-the-art HiFi sequencing technology to
offer profound insights into genetic diversity, disease mechanisms,
and clinical diagnoses within Singapore’s multi-ethnic
population.
This partnership highlights the critical role of PacBio's HiFi
sequencing technology in advancing precision medicine. Beyond the
capabilities of traditional short-read sequencing technologies,
PacBio's long-read sequencing provides comprehensive genomic
coverage, enabling the detection of large structural variations and
DNA methylation, providing a more complete picture of the genome.
This multi-omics approach, combining whole genome sequencing (WGS),
RNA full-length sequencing, fibre sequencing, and methylation
analysis, positions PacBio as an essential contributor to the
success of this joint effort with PRECISE.
"I am delighted that PRECISE has selected our Revio system for
their extensive, flagship long-read sequencing project in
Singapore," said Christian Henry, President and Chief
Executive Officer of PacBio. "PRECISE chose PacBio HiFi
technology for its capacity to deliver complete and accurate
genomes. This project exemplifies Revio’s unique ability to provide
differentiated solutions for large-scale, multi-thousand-sample,
whole genome sequencing projects."
PacBio's joint effort with PRECISE is set to elevate precision
medicine in Singapore, leveraging highly-accurate long-read
sequencing to drive scientific breakthroughs and enhance clinical
outcomes. Through significant product contributions, investment in
local expertise, and a comprehensive data platform, PacBio is
dedicated to the success of this transformative initiative.
Key highlights of the partnership
Comprehensive Long-Read Genomic Data
PacBio will generate high-quality phased methylome and genomic
information for a multi-thousand-sample whole genomes sequencing
project, including:
- 60x HiFi depth for
Pan-Asian reference genomes.
- 20x HiFi depth for
multi-omics analysis.
- 30x HiFi depth for
unresolved and research cases in cancer and rare diseases.
Advanced Sequencing Infrastructure
PacBio will establish advanced sequencing and data analysis
pipelines in Singapore, including a centralised library preparation
facility and sequencing laboratory for high throughput
production.
Appointed Service Provider
Macrogen Asia Pacific Pte Ltd, the first CAP-accredited service
provider in Singapore for Whole Genome Sequencing (WGS), will
execute the PacBio long-read sequencing production.
Data Integration and Secure Access
PacBio will utilise AWS cloud storage and workflow capabilities
to ensure secure and efficient data processing and delivery for
PRECISE researchers and clinicians.
The comprehensive efforts outlined in this partnership
underscore the commitment of both PacBio and PRECISE to pioneering
advancements in genomic research and precision medicine. By
combining cutting-edge technology, extensive genomic data, and
dedicated local expertise, this joint effort is poised to deliver
ground breaking discoveries that can help shape the future of
healthcare in Singapore and beyond.
For more information, please contact:
Contacts (PacBio)
Investors: Todd Friedmanir@pacificbiosciences.com
Media:pr@pacificbiosciences.com
Contacts (Macrogen)
Media:chloeje@macrogen.com
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
stem from two highly differentiated core technologies focused on
accuracy, quality and completeness which include our HiFi long-read
sequencing and our SBB® short-read sequencing technologies. Our
products 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 Precision Health Research, Singapore
(PRECISE)Precision Health Research, Singapore (PRECISE) is
the central entity set up to coordinate a whole of Singapore effort
to implement Phase II of Singapore’s three-phase National Precision
Medicine (NPM) programme.
NPM Phase II aims to transform healthcare in Singapore and
improve patient outcomes through new insights into the Asian genome
and data-driven healthcare solutions. In NPM Phase II, PRECISE will
collaborate with Singapore research and clinical partners,
including the Agency for Science, Technology and Research (A*STAR),
Lee Kong Chian School of Medicine, National Healthcare Group,
National University Health System, National University of
Singapore, and SingHealth Duke-NUS Academic Medical Centre to study
the genetic makeup of 100,000 healthy Singaporeans and specific
patient cohorts. The genetic data will be integrated with detailed
lifestyle, environmental, and clinical data to yield rich insights
into factors that contribute to Asian diseases and conditions.
Additionally, NPM Phase II will enhance the breadth and
depth of the Precision Medicine-related industry by attracting and
anchoring overseas companies in Singapore, while yielding new
opportunities for home-grown companies. To enhance and accelerate
the precision medicine sector, PRECISE works in close collaboration
with A*STAR, the Biomedical Sciences Industry Partnership Office,
and the Economic Development Board to catalyse the next phase of
growth for Singapore’s healthcare and the biomedical technology
industries.
PRECISE is a programme of the Consortium for Clinical Research
and Innovation, Singapore (CRIS). PRECISE is supported by the
National Research Foundation, Singapore (NRF) under the RIE2020
White Space (MOH-000588 and MOH-001264) and administered by the
Singapore Ministry of Health through the National Medical Research
Council (NMRC) Office, MOH Holdings Pte Ltd.
For more information, visit www.npm.sg
About Macrogen
Macrogen provides genomics services for research use, as well as
clinical diagnostics worldwide, with laboratories in six countries
and more than 18,000 customers in 153 countries. Their research
services include Next Generation Sequencing, Capillary
Electrophoresis Sequencing, Microarrays, Transgenic mice, and
Oligonucleotide synthesis. Clinical services include hereditary
cancer testing, somatic cancer panels, carrier testing, NIPT
screening, clinical WGS, and clinical WES.
The laboratories in Singapore, USA, and Korea have received
College of American Pathologists (CAP) accreditation. Macrogen’s
main laboratory in Korea also holds certifications from the Korean
Institute of Genetic Testing Evaluation and the Korean Ministry of
Food and Drug Safety for NGS Clinical Laboratory.
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
uses, coverage, advantages, quality or performance of, or benefits
or expected benefits of using, PacBio products or technologies,
including in connection with Novogene’s anticipate use of Revio;
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, and the difficulty of generating discoveries across
various areas of research; potential product performance and
quality issues; third-party claims alleging infringement of patents
and proprietary rights or seeking to invalidate PacBio's patents or
proprietary rights; and other risks associated with international
operations. 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.
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