Technology
Next-Generation Sequencing Services Market Poised for Remarkable Growth: Projected to Increase from $7 Billion in 2024 to $15 Billion by 2031: – Market Research Intellect
Published
1 year agoon
By
The Next-Generation Sequencing (NGS) Services Market is driven by several key factors, including significant advancements in sequencing technologies that enhance accuracy and speed. The declining costs of sequencing are making it more accessible to researchers and healthcare providers. Additionally, the rising prevalence of genetic disorders and the growing emphasis on personalized medicine are fueling demand for NGS services.
LEWES, Del., Jan. 23, 2025 /PRNewswire/ — The Next-Generation Sequencing (NGS) Services Market is projected to grow from approximately USD 7 billion in 2024 to around USD 15 billion by 2031, achieving a compound annual growth rate (CAGR) of about 11%. This growth is fueled by advancements in sequencing technologies, reduced costs, and an increasing emphasis on personalized medicine and genetic research applications.
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202 – Pages
126 – Tables
37 – Figures
Scope Of The Report
REPORT ATTRIBUTES
DETAILS
STUDY PERIOD
2020-2031
BASE YEAR
2023
FORECAST PERIOD
2024-2031
HISTORICAL PERIOD
2020-2023
UNIT
Value (USD Billion)
KEY COMPANIES PROFILED
Illumina, Inc., Thermo Fisher Scientific Inc., Pacific Biosciences of California, Inc., Roche Diagnostics, BGI Genomics Co., Ltd., Agilent Technologies, Inc., QIAGEN N.V., PerkinElmer, Inc., Bio-Rad Laboratories, Inc., and Oxford Nanopore Technologies Ltd.
SEGMENTS COVERED
By Type, By Application And By Geography
CUSTOMIZATION SCOPE
Free report customization (equivalent to up to 4 analysts’ working days) with purchase. Addition or alteration to country, regional & segment scope
Next-Generation Sequencing (NGS) Services Market Overview
Market Growth and Size
The Next-Generation Sequencing (NGS) Services Market is on a robust growth trajectory, expected to expand from approximately USD 7 billion in 2024 to around USD 15 billion by 2031. This impressive growth reflects a compound annual growth rate (CAGR) of about 11%. Several factors contribute to this upward trend, including the increasing demand for genomic analysis across various sectors, such as healthcare, agriculture, and personalized medicine. As more research institutions and healthcare providers adopt NGS technologies, the market is likely to witness heightened investment in innovative sequencing solutions. Furthermore, the rising incidence of genetic disorders and the need for accurate diagnostic tools will continue to stimulate market expansion. This growth presents significant opportunities for key players and stakeholders in the NGS industry to enhance their service offerings and meet the evolving needs of end-users.
Technological Advancements
Technological advancements play a pivotal role in shaping the Next-Generation Sequencing Services Market. Innovations in sequencing technologies, such as improved algorithms and automated systems, have significantly enhanced the speed and accuracy of genomic analysis. Companies are increasingly developing high-throughput sequencing platforms that allow for the rapid processing of large volumes of genetic data. Additionally, advancements in bioinformatics tools enable more efficient data analysis and interpretation, making it easier for researchers to derive meaningful insights from genomic information. These technological breakthroughs are not only reducing the costs associated with sequencing but also expanding its applications in various fields, including oncology, reproductive health, and infectious diseases. As technology continues to evolve, it will likely pave the way for new services and applications within the NGS market, driving further growth and innovation.
Rising Demand for Personalized Medicine
The growing emphasis on personalized medicine is a significant driver of the Next-Generation Sequencing Services Market. As healthcare shifts towards more individualized treatment approaches, the need for precise genomic information becomes paramount. NGS technologies enable the identification of genetic variations that can influence drug efficacy and patient response, leading to tailored treatment plans that enhance patient outcomes. The application of NGS in oncology, for example, allows for the profiling of tumors to identify specific mutations, guiding targeted therapy decisions. Additionally, advancements in pharmacogenomics, which studies how genes affect a person’s response to drugs, further fuel demand for NGS services. As healthcare providers increasingly recognize the value of personalized medicine, the NGS market is expected to expand significantly, with more providers integrating these services into their practice to deliver optimized patient care.
Application in Clinical Diagnostics
Next-Generation Sequencing is becoming an integral component of clinical diagnostics, transforming the way genetic disorders are diagnosed and managed. The ability to sequence entire genomes or targeted gene panels allows for the identification of genetic mutations associated with various diseases. This capability enhances diagnostic accuracy and provides critical information for patient management and treatment decisions. For instance, NGS is widely used in prenatal testing, cancer diagnostics, and rare disease identification, enabling early intervention and improved outcomes. As regulatory bodies increasingly approve NGS-based diagnostic tests, healthcare providers are more likely to adopt these technologies, driving market growth. The integration of NGS into clinical workflows also facilitates the development of companion diagnostics, which further enhances the personalization of treatment strategies. This trend underscores the importance of NGS in modern healthcare and its potential to revolutionize clinical diagnostics.
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Increasing Research Initiatives
The Next-Generation Sequencing Services Market is also benefitting from a surge in research initiatives across academia and industry. Governments, research institutions, and private organizations are investing significantly in genomics research to explore the genetic basis of diseases, improve agricultural practices, and advance biotechnology. This influx of funding is facilitating the establishment of large-scale genomic projects and biobanks that utilize NGS technologies to generate vast datasets for analysis. Collaborative efforts among researchers, institutions, and industry stakeholders are also driving innovation and expanding the applications of NGS in various fields, including environmental science and conservation. As research initiatives continue to grow, they will contribute to the advancement of NGS technologies and methodologies, ensuring a steady demand for sequencing services. This dynamic environment fosters a culture of discovery and innovation, positioning NGS as a cornerstone of modern scientific inquiry.
Challenges and Limitations
Despite its significant growth prospects, the Next-Generation Sequencing Services Market faces several challenges and limitations. One major concern is the complexity of data generated by NGS technologies, which can lead to data management and analysis difficulties. The sheer volume of genomic data requires sophisticated bioinformatics tools and skilled personnel to interpret the results accurately. Additionally, the high initial costs associated with implementing NGS platforms may pose a barrier for smaller laboratories and healthcare facilities. Regulatory challenges also exist, particularly in ensuring the quality and reliability of NGS-based diagnostic tests. Moreover, ethical considerations surrounding genetic data privacy and consent remain critical issues that the industry must address. Overcoming these challenges will be essential for the continued growth and adoption of NGS services, necessitating collaboration among industry stakeholders to develop standardized practices and solutions.
Competitive Landscape
The competitive landscape of the Next-Generation Sequencing Services Market is characterized by a diverse range of players, including established companies and emerging startups. Major industry leaders are continually innovating and expanding their service portfolios to maintain a competitive edge. Strategic collaborations, partnerships, and acquisitions are common as companies seek to enhance their technological capabilities and market reach. Additionally, the entry of new players with specialized NGS services is intensifying competition, driving further advancements in technology and service offerings. As the market evolves, companies are focusing on providing integrated solutions that encompass sequencing, bioinformatics, and data analysis, catering to the diverse needs of researchers and clinicians. This dynamic competitive environment encourages continuous improvement and innovation, ultimately benefiting end-users and advancing the field of genomics.
Future Outlook
The future outlook for the Next-Generation Sequencing Services Market is exceptionally promising, with sustained growth anticipated through 2031 and beyond. As genomic technologies continue to evolve, the scope of NGS applications is expected to expand, encompassing areas such as personalized medicine, precision agriculture, and infectious disease monitoring. The increasing integration of artificial intelligence and machine learning in genomic data analysis will enhance the accuracy and efficiency of NGS services, making them even more valuable to researchers and healthcare providers. Furthermore, ongoing collaborations between public and private sectors will likely accelerate research and development efforts, driving innovation in NGS technologies. As awareness of the importance of genomics in healthcare and research continues to rise, the NGS services market will play a crucial role in shaping the future of medicine and biotechnology, offering vast opportunities for growth and development.
Geographic Dominance:
The Next-Generation Sequencing (NGS) Services Market exhibits significant geographic dominance, particularly in North America and Europe. North America holds a substantial share, driven by advanced healthcare infrastructure, high investments in research and development, and the presence of leading biotechnology and pharmaceutical companies. The U.S. is at the forefront of NGS innovation, with numerous academic institutions and laboratories leveraging these technologies for cutting-edge research. Europe follows closely, with countries like Germany, the UK, and France investing heavily in genomics and personalized medicine initiatives. Additionally, the Asia-Pacific region is emerging as a key player, with increasing adoption of NGS technologies in countries like China and Japan, driven by government support and growing healthcare expenditures. As awareness of genomic applications expands globally, the NGS market is expected to witness significant growth across various regions, fostering a competitive landscape.
Next-Generation Sequencing (NGS) Services Market Key Players Shaping the Future
Key players shaping the future of the Next-Generation Sequencing (NGS) Services Market include Illumina, Inc., Thermo Fisher Scientific Inc., Pacific Biosciences of California, Inc., Roche Diagnostics, BGI Genomics Co., Ltd., Agilent Technologies, Inc., QIAGEN N.V., PerkinElmer, Inc., Bio-Rad Laboratories, Inc., and Oxford Nanopore Technologies Ltd. These companies are at the forefront of innovation, driving advancements in NGS technologies and expanding their service offerings to meet the growing demand for genomic analysis across various applications, from clinical diagnostics to research and development.
Next-Generation Sequencing (NGS) Services Market Segment Analysis
The Next-Generation Sequencing (NGS) Services market is segmented based on By Type, By Application and Geography, offering a comprehensive analysis of the industry.
1. By Type
Whole Genome Sequencing (WGS): This method involves sequencing the entire genome of an organism, providing comprehensive genetic information. WGS is used in various applications, including population genetics, evolutionary biology, and personalized medicine, enabling a thorough understanding of genetic variations and their implications.Targeted Sequencing: Focused on specific areas of interest within the genome, targeted sequencing is more cost-effective and faster than WGS. It is commonly used in clinical diagnostics to identify mutations associated with particular diseases, making it essential for cancer genomics and inherited disorders.Exome Sequencing: This technique sequences only the coding regions of genes, known as exomes. Exome sequencing is widely used in rare disease research and cancer studies, providing valuable insights while reducing the amount of data that needs to be analyzed compared to WGS.RNA Sequencing (RNA-seq): RNA-seq analyzes the transcriptome, offering insights into gene expression and regulation. This method is crucial for understanding diseases at the molecular level, particularly in cancer research and developmental biology, where gene expression patterns play a significant role.Other Sequencing Types: This category may include techniques such as methylation sequencing and amplicon sequencing, which serve specific research purposes. These methods contribute to the understanding of epigenetic modifications and targeted genomic regions, respectively.
2. By Application
Clinical Diagnostics: NGS plays a crucial role in identifying genetic mutations linked to various diseases, including cancers and hereditary disorders. The ability to provide accurate and timely diagnoses enhances patient management and treatment strategies, driving the demand for NGS services in clinical settings.Drug Discovery: In the pharmaceutical industry, NGS is leveraged to identify potential drug targets and understand disease mechanisms at the molecular level. By enabling researchers to analyze genetic variations, NGS accelerates the drug development process and helps in the design of personalized therapies.Biomarker Discovery: NGS is instrumental in discovering and validating biomarkers for disease diagnosis and prognosis. This application is particularly relevant in oncology, where identifying specific genetic alterations can inform treatment decisions and improve patient outcomes.Agriculture: NGS technologies are increasingly used in agricultural research to enhance crop traits and improve food security. By analyzing the genomes of plants and animals, researchers can identify beneficial traits, develop genetically modified organisms, and improve breeding programs.Environmental Testing: NGS is applied in environmental studies to monitor biodiversity and assess ecosystem health. By sequencing microbial communities and assessing their genetic composition, researchers can gain insights into environmental changes and their implications for public health and conservation efforts.
3. Geography
North America: This region dominates the NGS Services Market due to its advanced healthcare infrastructure, high research funding, and the presence of leading biotechnology companies. The U.S. is a key player in NGS innovation, driving significant market growth through technological advancements and widespread adoption of genomic technologies.Europe: Europe follows closely, with countries like Germany, the UK, and France investing heavily in genomics and personalized medicine initiatives. The European market is characterized by collaborations among research institutions, universities, and industry stakeholders, fostering innovation and expanding the use of NGS services.Asia-Pacific: The Asia-Pacific region is emerging as a significant market for NGS services, driven by increasing healthcare expenditures and government support for research initiatives. Countries like China and Japan are at the forefront of adopting NGS technologies, with a focus on genomics research and clinical applications.Latin America: The Latin American NGS market is experiencing growth as awareness of genomic technologies increases among healthcare providers and researchers. Emerging economies in this region are gradually adopting NGS for clinical diagnostics and research, creating opportunities for market expansion.Middle East & Africa: The NGS Services Market in the Middle East and Africa is in its early stages but shows potential for growth. Increasing investments in healthcare infrastructure and research initiatives are expected to drive demand for NGS services in these regions, although challenges such as limited access to advanced technologies persist.
Pharma And Healthcare:
The Pharma and Healthcare segment of the Next-Generation Sequencing (NGS) Services Market is experiencing significant growth, driven by the increasing demand for personalized medicine and advancements in genomics. NGS technologies facilitate the comprehensive analysis of genetic variations, enabling healthcare providers to tailor treatments based on individual patient profiles. This is particularly impactful in oncology, where genomic sequencing can identify mutations that inform targeted therapies. Additionally, NGS plays a critical role in clinical diagnostics, allowing for the early detection of genetic disorders and enhancing disease management strategies. As pharmaceutical companies integrate NGS into drug development processes, the ability to identify novel biomarkers accelerates the discovery of effective therapies. The rising prevalence of chronic diseases and genetic conditions further fuels the adoption of NGS services in healthcare settings. Overall, the Pharma and Healthcare segment is poised for continued expansion, contributing significantly to the overall growth of the NGS Services Market.
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Technology
BillionToOne Launches Unity Confirm™: A category-defining test that bridges the gap between screening and invasive diagnostics
Published
15 minutes agoon
May 1, 2026By
A breakthrough in prenatal care, Unity Confirm enables non-invasive confirmation for high-risk screening results through the capture of intact circulating fetal cells using BillionToOne’s Fetal Cell Capture™ Technology
MENLO PARK, Calif., May 1, 2026 /PRNewswire/ — For more than two decades, the ultimate quest for scientists and clinicians studying prenatal genetics was the capture of an intact fetal cell non-invasively so that its fetal DNA could be directly analyzed. While cell-free DNA has revolutionized prenatal genetics, it left an uncertainty—a gap between screening and invasive diagnostics, for patients who cannot, or choose not to, access invasive diagnostics. Today, BillionToOne, Inc. (Nasdaq: BLLN), a next-generation molecular diagnostics company with a mission to create powerful and accurate tests that are accessible to all, announced the launch of Unity Confirm™, a circulating fetal cell-based, non-invasive confirmation test, designed to address this need from a simple maternal blood draw.
Since its introduction in the early 2010s, non-invasive prenatal testing (NIPT) has become the standard of care for screening for fetal aneuploidies. However, when screening returns a high-risk result, clinical guidelines recommend diagnostic confirmation via chorionic villus sampling (CVS) or amniocentesis. These invasive procedures carry a small but real risk of pregnancy loss, and are increasingly difficult to access. The majority of patients decline, leaving clinicians and families without the information needed to guide next steps, and widening gaps in inequitable care.
While cell-based prenatal genetics has been studied since before the advent of cell-free DNA tests, the scientific barrier has long been the rarity and fragility of fetal cells in maternal circulation. Presenting at fewer than one cell per milliliter of blood and nearly indistinguishable from millions of surrounding maternal cells, intact circulating fetal cells have been too difficult to isolate in an accessible way for clinical use. The cell-based approaches were previously studied across multiple independent publications1 in more than 1,500 patients, consistently demonstrating that when a fetal cell is captured and sequenced, it provides an accurate result that has extremely high concordance with invasive diagnostic testing. However, these methodologies have stayed too academic, expensive, and inaccessible.
Unity Confirm addresses this directly. Available for all patients who use UNITY Aneuploidy for their front-line screen*, BillionToOne’s Fetal Cell Capture™ technology, a multi-step immunological enrichment and single cell isolation process, isolates intact circulating fetal cells, effectively providing 100% fetal fraction2, and performs whole genome sequencing on each individual cell. By analyzing the direct fetal cells rather than fragmentary cfDNA, similar to invasive procedures, Unity Confirm delivers rapid CVS-like insights3 non-invasively, from a single blood draw.
“For years, the idea of capturing whole fetal cells non-invasively was largely viewed as an elusive holy grail, something theoretically possible but practically out of reach,” said Oguzhan Atay, PhD, Co-founder and CEO of BillionToOne. “Unity Confirm is proof that it does not have to be. For the first time, a clinician can confirm a high-risk prenatal result non-invasively, with a level of accuracy the field has never before seen outside of an invasive procedure. For the first time, this technology is broadly accessible.”
“A high-risk NIPT result does not give you a diagnosis. It gives you a decision to make under enormous stress, often without enough information,” said Haywood Brown, MD, Chief Medical Officer, Prenatal, BillionToOne. “For too long, the options were limited: forgo confirmation, or undergo an invasive procedure with a small but real risk. What makes Unity Confirm truly different is not just the science; it is that this capability is now clinically accessible. That’s not an incremental improvement. That is a fundamentally different standard of care.”
In BillionToOne’s own clinical validation, Unity Confirm demonstrated 100% concordance with known fetal outcomes and invasive diagnostic results across 16 of 16 samples, including affected fetuses for common aneuploidies and 22q11.2 microdeletion. The clinical data supporting Unity Confirm will be presented at ACOG 2026 in Washington, D.C., presenting the science behind the technology to the broader OB/GYN community for the first time. Beginning on May 28, providers using Unity Aneuploidy™ Screen will have access to Unity Confirm following a high-risk result. To further validate performance at scale, BillionToOne is now enrolling in the largest prospective study of a fetal cell-based confirmation assay with invasive diagnostic outcomes, targeting enrollment of 1,000 patients and measuring concordance to invasive diagnostic testing.
*Unity Confirm is intended for patients who cannot, or choose not to, pursue invasive diagnostic testing following a high-risk Unity Aneuploidy Screen result before 16 weeks of gestation. Available for Trisomy 21 (Down syndrome), Trisomy 18, Trisomy 13, 22q11.2 microdeletion, XXY, XYY, and XXX aneuploidies. Requires Unity Aneuploidy Screen as the frontline screen for the pregnancy.
Sources
1Hatt, Lotte, et al. “A new marker set that identifies fetal cells in maternal circulation with high specificity.” Prenatal Diagnosis 34.11 (2014): 1066-1072.; Stampalija, T., et al. “Single-cell-based non-invasive screening for fetal pathogenic microimbalances using maternal blood: comparison with invasive prenatal diagnosis.” Ultrasound in Obstetrics & Gynecology (2026).; Weymaere, Jana, et al. “Enrichment of circulating trophoblasts from maternal blood using filtration-based Metacell® technology.” Plos one 17.7 (2022):e0271226.; Jeppesen, Line Dahl, et al. “Screening for Fetal Aneuploidy and Sex Chromosomal Anomalies in a Pregnant Woman with Mosaicism for Turner Syndrome—Applications and Advantages of Cell-Based NIPT.” Frontiers in Genetics 12 (2021): 741752.; Bellair, Michelle, et al. “Noninvasive single-cell-based prenatal genetic testing: A proof of concept clinical study.” Prenatal Diagnosis 44.3 (2024):304-316.; Chakchouk, Imen, and Ignatia B. Van den Veyver. “Whole-Genome Amplification on Single Circulating Trophoblast Cell.” Whole Genome Amplification: Methods and Protocols. New York, NY: Springer US, 2026. 11-23.; Zhuo, Xinming, et al. “Use of amplicon-based sequencing for testing fetal identity and monogenic traits with Single Circulating Trophoblast (SCT) as one form of cell-based NIPT.” PLoSOne 16.4 (2021): e0249695.
2In rare instances, results may rely on a single cell that is co-sequenced with 1-2 maternal cells, which may reduce fetal fraction to 50% or 33%. When this occurs, the report clearly indicates this limitation.
3Unity Confirm and rapid CVS both analyze fetal-derived trophoblast cells. Unity Confirm isolates individual cells via whole genome sequencing (WGS), which is performed on each cell separately, whereas rapid CVS is often performed via FISH. While rapid CVS may analyze more cells, WGS generates more data per cell. In both rapid CVS and fetal cell capture, mosaicism cannot be excluded. Unity Confirm may have false-positive and false-negative results. Results are not a guaranty. Important medical decisions should not rely on UnityConfirm test results alone. Clinical correlation is necessary. Unity Confirm is a laboratory-developed test performed in a CLIA-certified and CAP-accredited laboratory. It is not an FDA-approved or FDA-cleared diagnostic test. Test performance may vary based on gestational age and other factors.
Forward-Looking Statements
This press release contains certain forward-looking statements within the meaning of federal securities laws. These forward-looking statements generally are identified by the words “believe,” “project,” “expect,” “anticipate,” “estimate,” “intend,” “strategy,” “future,” “opportunity,” “plan,” “may,” “should,” “will,” “would,” “will be,” “will continue,” “will likely result,” and similar expressions. Forward-looking statements are predictions, projections and other statements about future events that are based on current expectations and assumptions and, as a result, are subject to risks and uncertainties. Forward-looking statements in this press release include, but are not limited to, statements regarding the clinical effectiveness of Unity Confirm. These statements are based on management’s current expectations, forecasts and assumptions, and actual outcomes and results could differ materially from these statements due to a number of factors, some of which are beyond BillionToOne’s control. These and additional risks and uncertainties could affect BillionToOne’s financial and operating results and cause actual results to differ materially from those indicated by the forward-looking statements made in this press release. These risks and uncertainties include, but are not limited to, the risk that Unity Confirm is not clinically effective and not adopted by healthcare professionals and those discussed under the captions “Risk Factors” and “Management’s Discussion and Analysis of Financial Condition and Results of Operation” and elsewhere in BillionToOne’s most recently filed Annual Report on Form 10-K, and other filings we make with the Securities and Exchange Commission from time to time. The forward-looking statements in this press release are based on information available to BillionToOne as of the date hereof, and BillionToOne disclaims any obligation to update any forward-looking statements provided to reflect any change in its expectations or any change in events, conditions, or circumstances on which any such statement is based, except as required by law. These forward-looking statements should not be relied upon as representing BillionToOne’s views as of any date subsequent to the date of this press release.
About BillionToOne
Headquartered in Menlo Park, California, BillionToOne is a next-generation molecular diagnostics company with a mission to create powerful and accurate tests that are accessible to all. The company’s patented Quantitative Counting Templates™ (QCT™) molecular counting platform is the only multiplex technology that can accurately count DNA molecules at the single-molecule level. For more information, visit www.billiontoone.com.
Media Contact
billiontoone@moxiegrouppr.com
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Brockton High School Students Premiere Original Films Exploring Mental Wellness and Leadership
Twenty-three student creators showcase cinematic takes on boundaries, bias, and leadership; selected works to advance to the National SALT 12 Film Festival.
BROCKTON, Mass., May 1, 2026 /PRNewswire-HISPANIC PR WIRE/ — Brockton High School hosted the 2026 Brockton High School Film Festival, a community celebration of student voice and mental wellness. Organized by the nonprofit SALT ED Inc., the event premiered five original short films created by 23 students participating in the “Reel Funny” program.
Unlike traditional film programs, Reel Funny uses media production as a vehicle for personal growth rather than just technical instruction. The program guides students through a series of workshops focused on “soft skills”—including conflict resolution, recognizing internal bias, and establishing healthy personal boundaries. Students are then challenged to apply these lessons by collaborating in groups to write, produce, and edit their own films entirely independently.
A unique and critical component of the Reel Funny process is its integration of mental health professional oversight. Following the students’ film submissions, Eun Joo You, a Licensed Clinical Social Worker (LCSW) with Care Plus New Jersey, conducted a specialized screening of the works. This clinical review serves to evaluate student mental wellness and identify early signs of emotional distress, followed by direct engagement with the students to discuss their creative themes and overall well-being.
“The opportunity for our students to engage in this type of work is paramount to their development as well-rounded individuals,” said Kevin McCaskill, Principal of Brockton High School. “When we talk about preparing the next generation of leaders, we aren’t just talking about academics; we are talking about the emotional intelligence and self-awareness that programs like ‘Reel Funny’ provide. These films are a powerful reflection of their growth.”
The celebration invited friends, families, and local community members to acknowledge the leadership and vulnerability displayed by these young creators.
“This program empowers students to turn self-reflection into a leadership tool,” said Joonho Lee, CEO of Kbean®, a primary supporter of the initiative. “By giving students the autonomy to produce these films on their own terms, we see a level of authenticity that traditional education often misses.”
Looking Ahead: The SALT 12 National Showcase
The Brockton High School festival serves as a qualifying event for the 3rd Annual SALT 12 Film Festival scheduled for the end of 2026. SALT 12 is a national platform that gathers the most impactful student films from across the country, allowing participants to share their voices with a public audience and compete for national recognition.
For more information about SALT ED Inc., the Reel Funny curriculum, or the upcoming SALT 12 National Showcase, please visit www.salt-ed.org.
About SALT ED Inc.
SALT ED Inc. is a nonprofit organization dedicated to empowering underserved youth through media production, workforce development, and mental wellness initiatives. Their signature “Reel Funny” program helps students develop the emotional intelligence and leadership skills necessary to succeed as next-generation leaders.
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SOURCE Kbean
Technology
Products That Count Announces the Winners of the 2026 CPO Awards, Honoring the Product Leaders Redefining Their Craft in the AI Era
Published
1 hour agoon
May 1, 2026By
The annual Awards recognize Chief Product Officers whose scope, influence, and impact have expanded dramatically as AI reshapes every organization.
SAN FRANCISCO, May 1, 2026 /PRNewswire-PRWeb/ — Products That Count, the world’s largest nonprofit community of product managers with over 600,000 members, today announced the winners of the 2026 CPO Awards. The Awards, produced in partnership with Mighty Capital, celebrate the Chief Product Officers whose leadership is shaping how products are built, shipped, and scaled in a moment of unprecedented change.
The role of the Chief Product Officer has never been broader. Today’s CPOs are architecting the systems, teams, and decisions that determine whether their companies win in the AI era.
The 2026 CPO Award Winners, by category:
President / CEO: Former CPOs who have elevated to the top role.
Eglae Recchia, CPO, Keyway
Maria Thomas, CEO (promoted from CPO), Rebrandly
Nabil Bukhari, President, Extreme Networks
Shiven Ramji, President & Chief Product Officer, Okta
Investor Mindset: Treating product like a portfolio of bets, with M&A as a strategic lever.
Achuth Rao, CPO, New York Life Insurance Company
Andrew Tsao, CPO & Analytics Officer, Audible
Dane Glasgow, CPO, Paramount/Skydance
Diana Benli, Chief Product Officer, Cognizant
Diego Dugatkin, Chief Product Officer, Box
Mike Bidgoli, CPO & CTO, Tubi
Vasu Murthy, CPO, Cohesity
Vrushali Paunikar, CPO, Carta
Ambrish Verma, Chief Product Officer, Ingram Micro
Enterprise Scale: Operating in complexity. Not speed alone, but transformation at scale.
Carla Guzzetti, Chief Product Officer, Cloud Applications, Extreme Networks
Eddie Garcia, Chief Product Officer, eBay
Gautam Shah, Chief Product Officer, Carelon
Ghazal Badiozamani, SVP of Product Management, Cengage
Kelli Fielding, Chief Product Officer, Europe, TransUnion
Mikhail Vaysbukh, Chief Product Officer, Elsevier
Monica Ugwi, GM, Copilot + Agents for Manufacturing & Mobility, formerly Microsoft
Randall Hounsell, SVP Connected Living Product, Comcast
Rita Khan, Chief Consumer & Digital Officer, formerly Optum
Ryan Bergstrom, Chief Product Officer, Paychex
Tim Simmons, Chief Product Officer, formerly Walmart International
Tina Tarquinio, Chief Product Officer, IBM Z and LinuxONE, IBM
Todd Garner, CPO, Sam’s Club
Trey Courtney, Global Chief Product & Partnerships Officer, Mood Media
Wyatt Jenkins, SVP Product, Intuit
Shayani Roy, SVP Product Management and Design, OpenTable
Scale Up: Growth-stage leaders putting the scale in place.
Aaron Seevers, Chief Product Officer, Noom
Avijit Sinha, SVP Corporate Development, EDB
Hannah Park, Chief Product Officer, Planned Parenthood
Joe Futty, CPO & CTO, Pipedrive
Jonathan Shottan, Chief Product Officer, Tonal
Kimberly Bloomston, CPO, 6sense
Kousthub Raghavan, Chief Product & Digital Officer, CLEAR
Natalia Williams, Chief Product Officer, Qonto
Nikita Miller, Chief Product Officer, Perk
Nilesh Khandelwal, Chief Product Officer, Rakuten Rewards
Paul Burke, CPO, Reveleer
Randhir Vieira, CPO, formerly Healthify
Renn Turiano, CPO, Gannett – USA Today Network
Sarah Turrin, CPO, Color
Emerging: On an amazing trajectory, regardless of tenure.
Adam Kelsey, EVP, Product Management, SignalWire
Apurva Garware, SVP, Head of Product, Invisible Technologies
Chai Atreya, Chief Product Officer, ActiveCampaign
Jack Brody, Chief Product Officer, Suno
John Barrus, VP of Product Management, Niobium
Kevin Swint, former Co-Founder & CPO, RemixAI
Nirmal Kumar, CPO, Aliaswire
Rafael Flores, Chief Product Officer, Treasure Data.ai
Sarah Jacob Singh, CPO & CTO, Medbridge
Sarosh Waghmar, CPO & Co-Founder, Spotnana
Vanessa Davis, CPO, LegalOn
Vikas Seth, CPO, ARIS
Platform: Multiplying impact beyond their own product by leveraging the ecosystem at scale.
Arnab Bose, CPO, Asana
Kishan Chetan, EVP & GM, Agentforce Service Cloud, Salesforce
Shardul Vikram, Chief Product Officer, SAP Application AI, SAP
Tom Occhino, Chief Product Officer, Vercel
Rohit Badlaney, CPO & General Manager, IBM Cloud Platform, IBM
Terre Layton, former CPO, BetterHealth
B.J. Boyle, Chief Product Officer, MacroHealth
Winners were selected by an Independent Advisory Council of seasoned product executives based on impact and leadership.
ABOUT PRODUCTS THAT COUNT
Products That Count is the world’s largest nonprofit community, engaging 600,000+ product managers and Chief Product Officers (CPOs) united by a mission: to empower everyone to build products that truly count. In a world flooded with products, only a few ignite passion, deliver value at scale, and transform lives. Behind those exceptional products are visionary CPOs and high-performing product teams driving innovation at the most bleeding-edge companies. We recognize these trailblazers through our coveted Awards, accelerate careers from PM to the C-suite and beyond through daily best practices, and serve as the trusted advisor to nearly all Fortune 1000 CPOs. Our Corporate Alliance includes Walmart, Ford, Cisco, Johnson & Johnson, Amplitude, and more. The most admired product leaders across industries serve on our Advisory Council, guiding the future of product leadership. Together, we’re shaping a future where every product counts. Learn more at productsthatcount.org
ABOUT MIGHTY CAPITAL
Mighty Capital is the VC firm that leverages the Product Alpha Effect, a data-backed framework for outperformance that proves great products drive great businesses. Founded in 2018 by SC Moatti, a product visionary and former Meta product leader, and Jennifer Vancini, a veteran of tech investing and M&A, we bring a differentiated edge to venture. Through Moatti’s 600,000-strong Products That Count network of product leaders, we see where the world is going before others do. That proprietary signal gives us an advantage in sourcing, diligence, and post-investment value creation. Our portfolio speaks for itself: 1 in 5 companies is a category leader like Amplitude (NASDAQ:AMPL), Groq, and Netskope (NASDAQ:NTSK). Founders consistently call us the most value-add investor on their cap table, and use our global product ecosystem as a marketplace to accelerate time to revenue, scale, and exit. Anchored by GCM Grosvenor, we’re deploying Fund III with both prior funds in top decile DPI and TVPI, more than $20B in value created, and 6 IPOs to date. Learn more at Mighty.Capital.
Media Contact
Emma Shirlin, Products That Count, 1 8287020154, emmashirlin@productsthatcount.com
View original content:https://www.prweb.com/releases/products-that-count-announces-the-winners-of-the-2026-cpo-awards-honoring-the-product-leaders-redefining-their-craft-in-the-ai-era-302759934.html
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