Resources
About Us
Next-Generation Sequencing (NGS) Market: Industry Outlook by Offering (Sample Preparation [DNA Extraction, Library Preparation, Automation], Systems, Bioinformatics, Sequencing Services) Application (Clinical, Research) End User — Global Forecast to 2031
Report ID: MRHC - 1041274 Pages: 451 Jul-2024 Formats*: PDF Category: Healthcare Delivery: 2 to 4 Hours Download Free Sample ReportThe NGS Market is projected to reach $42.7 billion by 2031 at a CAGR of 15.7% from 2024 to 2031. The growth of the NGS market is driven by the rising cancer prevalence & the increasing application of NGS in cancer treatment and research, partnerships between NGS service providers & pharmaceutical companies, technological advancements in NGS, the growing demand for optimized & streamlined NGS workflows, the declining costs of genome sequencing, technological advancements in sequencing procedures, technological advancements in NGS informatics solutions, increasing pharmaceutical R&D expenditures, the surge in genome mapping programs, and improvements in regulatory & reimbursement scenarios for NGS-based diagnostic tests.
Furthermore, the increasing applications of NGS, the rising adoption of bioinformatics and genomic data management solutions, collaborations between vendors to develop library preparation protocols, the growing use of bioinformatics and genomic data management solutions for large-scale data analysis and interpretation, the increasing adoption of NGS informatics tools among hospitals and clinical laboratories, and government initiatives supporting large-scale genomic sequencing projects are expected to generate growth opportunities for the players operating in the NGS market.
Cancer is a major cause of death and a prominent obstacle in improving life expectancy globally. According to GLOBOCAN, the number of new cancer cases is expected to increase from 19.2 million in 2020 to 24.5 million in 2030. In addition, mortalities from cancer are expected to increase from 9.9 million in 2020 to 12.9 million in 2030. Thus, the increasing prevalence of cancer is expected to boost the adoption of NGS in clinical settings. Next-generation Sequencing (NGS) is considerably contributing to researchers’ understanding of cancer biology. Genomics research supported by NGS has identified genetic heterogeneity even among cancer types that were earlier considered identical. The discovery of unique molecular signatures is helping in the development of potential cancer treatments, increasing the demand for NGS in cancer research.
Click here to: Get Free Sample Pages of this Report
The need for genomic data drives the demand for next-generation sequencing. The huge volumes of data generated from NGS have created enormous pressure on healthcare providers in terms of data analysis, interpretation, reporting, and management. Data storage and computing tools save money and time while scaling production, keep data secure with monitoring by security and compliance, and easily share volumes of genomic data in multiple working groups with user and team-specific access.
Technological advancements in NGS informatics solutions have made it easier to create long sequencing runs, analyze sequencing data, monitor run status, and view results within shorter timeframes. Additionally, data flow from instruments can now be processed by software, making it easier to manage and analyze data using data analysis applications. NGS informatics technology has allowed the discovery of genetically targeted drugs and blood tests to detect cancer early. It has also enabled diagnoses for people with rare diseases. Thus, the technological advancements in NGS informatics solutions are expected to drive the growth of the NGS market.
Cheaper and well-established alternatives to next-generation sequencing (NGS) for cell molecular profiling, such as microarray, Fluorescence In Situ Hybridization (FISH), and Polymerase Chain Reaction (PCR), are readily available. These methods have traditionally been used in cancer cell molecular profiling to detect actionable genetic alterations or biomarkers. Other alternative technologies include Allele-specific array Comparative Genomic Hybridization (aCGH), Sanger dideoxy sequencing, pyrosequencing, Multiplex Ligation-dependent Probe Amplification (MLPA), and Mass Spectrometry (MS) for gene studies. Therefore, the availability of these alternative technologies restrain the adoption of NGS, impeding the growth of the NGS market.
Precision medicine is an emerging approach to patient care. Physicians choose a treatment method based on the patient’s genetic makeup, also considering genetic changes resulting from a disease and lifestyle habits. It is an emerging disease treatment & prevention approach that considers variability in genes, environments, and lifestyles among individuals. Precision medicine can reduce the need for guesswork (trial and error in medication depending on how the medication affects the patient’s symptoms), help physicians overcome challenges related to variable diagnostic ability, and aid the development of treatment strategies based on generalized demographics. Moreover, precision medicine provides a more holistic view of an individual’s health. In clinical workflows, precision medicine facilitates more predictive and preventive care through targeted therapies. Thus, the use of NGS in precision medicine to enable more personalized approaches is expected to create market growth opportunities.
NGS bioinformatics solutions offer additional features, such as data security and accuracy, by converting sequencing information into a standard format. This allows for the monitoring of instrument run quality and the streaming of data directly to on-premises or cloud servers. Moreover, benefits such as access to computing resources with minimum in-house infrastructure and increased efficiency with easy access to a multitude of genomic analysis applications have significantly increased the adoption of NGS bioinformatics solutions.
Based on offering, the NGS market is segmented into commercial sequencing/outsourced services, sample preparation, sequencing, and data analysis/bioinformatics. The commercial sequencing/outsourced services segment is further sub-segmented into targeted sequencing services, whole-genome sequencing services, RNA sequencing services, exome sequencing services, de novo sequencing services, ChIP sequencing services, methyl sequencing services, and other NGS services. In 2024, the commercial sequencing/outsourced services segment is expected to account for the largest share of 38.0% of the NGS market. The large market share of this segment can be attributed to the advantages offered by commercial sequencing/outsourced services, such as rapid delivery of results, access to advanced instruments and trained professionals, and lower costs compared to in-house sequencing.
Based on application, the market is segmented into research & other applications and clinical applications. In 2024, the research & other applications segment is expected to account for the largest share of 62.2% of the NGS market. The large market share of this segment can be attributed to the growing prevalence of genetic disorders, the increasing adoption of sequencing-based tests in laboratories, the growing demand for personalized medicines, and the increase in NGS-based research.
Based on end user, the NGS market is segmented into pharmaceutical & biotechnology companies, hospitals & diagnostic laboratories, academic & research institutes, and other end users. In 2024, the pharmaceutical and biotechnology companies segment is expected to account for the largest share of 43.5% of the NGS market. The large market share of this segment is attributed to the increasing R&D spending by pharmaceutical & biotechnology companies and the rising incidence of chronic diseases, which drive the adoption of next-generation sequencing products among pharmaceutical & biotechnology companies.
In 2024, North America is expected to account for the largest share of 48.7% of the NGS market. North America’s significant market share can be attributed to the increasing R&D expenditures in the pharmaceutical & biotechnology sector, the presence of leading NGS market players in the region, favorable government initiatives for genomics research, growing applications of NGS-based research, rising awareness of NGS-based tests, increasing prevalence of cancer and genetic diseases, and favorable reimbursement scenario in the region.
However, the market in Asia-Pacific is projected to register the highest growth rate of 16.9% during the forecast period. Countries such as China and India are anticipated to offer significant growth opportunities for the vendors in this market. Many Asia-Pacific nations are increasing their efforts to enhance the healthcare sector, leading to increased investments in improving healthcare accessibility, infrastructure, and drug discovery programs. Other key factors driving the growth of this regional market include the increasing incidence of cancer, rising adoption of advanced diagnostic and therapeutic technologies, and government initiatives promoting genome sequencing programs.
The report offers a competitive landscape based on an extensive assessment of the product offerings and geographic presence of leading market players and the key growth strategies adopted by them over the past few years. The key players operating in the global NGS market are Illumina, Inc. (U.S.), Thermo Fisher Scientific Inc. (U.S.), F. Hoffmann-La Roche Ltd. (Switzerland), Revvity, Inc. (U.S.), QIAGEN N.V. (Netherlands), Agilent Technologies, Inc. (U.S.), Pacific Biosciences of California, Inc. (U.S.), Danaher Corporation (U.S.), Oxford Nanopore Technologies Plc. (U.K.), MGI Tech Co., Ltd. (China), Tecan Group Ltd. (Switzerland), Beijing Genomics Institute (BGI) (China), Eppendorf AG (Germany), Hamilton Company (U.S.), Hudson Robotics (U.S.), LGC Limited (U.K.), Fabric Genomics, Inc. (U.S.), DNASTAR, Inc. (U.S.), Eurofins Scientific SE (Luxembourg), Novogene Co. Ltd. (China), and Quest Diagnostics Incorporated (U.S.).
In January 2024, Illumina Inc. (U.S.) signed an agreement with Janssen Research & Development, LLC (U.S.). The agreement marks the start of Illumina's novel molecular residual disease (MRD) assay, a whole-genome sequencing (WGS) multi-cancer research solution for detecting circular tumor DNA (ctDNA) for understanding the recurrence or persistence of disease following clinical intervention.
In March 2024, Thermo Fisher Scientific Inc. (U.S.) collaborated with Bayer AG (Germany) to develop NGS-based companion diagnostic assays (CDx) that offer decentralized genomic testing and rapid turnaround time to help increase patient access to Bayer’s precision cancer therapies.
Particulars |
Details |
Number of Pages |
451 |
Format |
|
Forecast Period |
2024-2031 |
Base Year |
2023 |
CAGR |
15.7% |
Estimated Market Size (Value) |
$42.7 billion by 2031 |
Segments Covered |
By Offering
By Application
By End User
|
Countries/Regions Covered |
North America (U.S. and Canada), Europe (Germany, France, U.K., Italy, Spain, and Rest of Europe), Asia-Pacific (China, Japan, India, and Rest of Asia-Pacific), Latin America (Brazil, Mexico, Rest of Latin America), and the Middle East & Africa |
Key Companies |
The key players operating in the global NGS market are Illumina, Inc. (U.S.), Thermo Fisher Scientific Inc. (U.S.), F. Hoffmann-La Roche Ltd. (Switzerland), Revvity, Inc. (U.S.), QIAGEN N.V. (Netherlands), Agilent Technologies, Inc. (U.S.), Pacific Biosciences of California, Inc. (U.S.), Danaher Corporation (U.S.), Oxford Nanopore Technologies Plc. (U.K.), MGI Tech Co., Ltd. (China), Tecan Group Ltd. (Switzerland), Beijing Genomics Institute (BGI) (China), Eppendorf AG (Germany), Hamilton Company (U.S.), Hudson Robotics (U.S.), LGC Limited (U.K.), Fabric Genomics, Inc. (U.S.), DNASTAR, Inc. (U.S.), Eurofins Scientific SE (Luxembourg), Novogene Co. Ltd. (China), and Quest Diagnostics Incorporated (U.S.). |
The global NGS market report covers the qualitative analysis and sizing of the market based on offering, application, and end user. It provides an analysis of these market segments at the regional and country level. The report also provides insights on factors impacting market growth, regulatory analysis, pricing analysis, and Porter’s five forces analysis.
The global NGS market is projected to reach $42.7 billion by 2031 at a CAGR of 15.7% from 2024 to 2031.
Among the offerings covered in this report, in 2024, the commercial sequencing/outsourced services segment is expected to account for the largest share of the NGS market. The large market share of this segment can be attributed to the advantages offered by commercial sequencing/outsourced services, such as rapid delivery of results, access to advanced instruments and trained professionals, and lower costs compared to in-house sequencing.
Among the applications covered in this report, in 2024, the research & other applications segment is expected to account for the largest share of the NGS market. The large share of the segment is attributed to the decreasing cost of sequencing procedures, increasing R&D by pharmaceutical and biotechnology companies for drug discovery, the increasing applications of NGS in multiple clinical and research settings, and the use of informatics solutions to find pharmacological targets, confirm therapeutic hypotheses, and predict the potential safety of inhibitory compounds aimed at molecular targets.
The growth of the NGS market is driven by the rising cancer prevalence & the increasing application of NGS in cancer treatment and research, partnerships between NGS service providers & pharmaceutical companies, technological advancements in NGS, the growing demand for optimized & streamlined NGS workflows, the declining costs of genome sequencing, technological advancements in sequencing procedures, technological advancements in NGS informatics solutions, increasing pharmaceutical R&D expenditures, the surge in genome mapping programs, and improvements in regulatory & reimbursement scenarios for NGS-based diagnostic tests.
Furthermore, the increasing applications of NGS, the rising adoption of bioinformatics and genomic data management solutions, collaborations between vendors to develop library preparation protocols, the growing use of bioinformatics and genomic data management solutions for large-scale data analysis and interpretation, the increasing adoption of NGS informatics tools among hospitals and clinical laboratories, and government initiatives supporting large-scale genomic sequencing projects are expected to generate growth opportunities for the players operating in the NGS market.
The key players operating in the global NGS market are Illumina, Inc. (U.S.), Thermo Fisher Scientific Inc. (U.S.), F. Hoffmann-La Roche Ltd. (Switzerland), Revvity, Inc. (U.S.), QIAGEN N.V. (Netherlands), Agilent Technologies, Inc. (U.S.), Pacific Biosciences of California, Inc. (U.S.), Danaher Corporation (U.S.), Oxford Nanopore Technologies Plc. (U.K.), MGI Tech Co., Ltd. (China), Tecan Group Ltd. (Switzerland), Beijing Genomics Institute (BGI) (China), Eppendorf AG (Germany), Hamilton Company (U.S.), Hudson Robotics (U.S.), LGC Limited (U.K.), Fabric Genomics, Inc. (U.S.), DNASTAR, Inc. (U.S.), Eurofins Scientific SE (Luxembourg), Novogene Co. Ltd. (China), and Quest Diagnostics Incorporated (U.S.).
Countries like China and India within Asia-Pacific are poised to offer significant growth opportunities for the vendors in this market. The growth of this regional market is driven by rapid economic growth across many countries, resulting in increased government focus on healthcare improvement. This has led to substantial investments in enhancing healthcare service accessibility, upgrading infrastructure, and fostering drug discovery and genome mapping initiatives.
Published Date: Jul-2024
Published Date: Jul-2024
Published Date: Jul-2024
Published Date: Jul-2024
Published Date: Feb-2024
Please enter your corporate email id here to view sample report.
Subscribe to get the latest industry updates