Whole Exome Sequencing Market Size, Share, Growth, and Industry Analysis, By Type (Agilent HaloPlex, Agilent SureSelect, Agilent SureSelect QXT, Illumina TruSeq Exome, Roche Nimblegen SeqCap and MYcroarray MYbaits), By Application (Correlation Research of Normal Human, Mendelian Disease and Rare Syndrome Gene Discovery, The Research of Complex Diseases and Mouse Exome Sequencing), and Regional Insights and Forecast to 2034

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WHOLE EXOME SEQUENCING MARKET OVERVIEW

The global Whole Exome Sequencing market size was USD 0.368 billion in 2025 and is projected to touch USD 1.083 billion by 2034, exhibiting a CAGR of 12.49% during the forecast period.

Whole Exome Sequencing (WES) is a next-generation sequencing (NGS) technique dedicated to sequencing only the protein-coding regions of the human genome, which are called exons. Exons represent only 1–2% of the human genome but hold roughly 85% of known disease-causing variants. The protocol begins with DNA extraction from any biological specimen, subsequently fragmenting the DNA, followed by the capturing of only exonic regions, before high-throughput sequencing. WES probes only the exons as opposed to the whole genome, which washes away sequencing costs and time, and still offers a comprehensive amount of information regarding the genetic basis of many diseases. Because of this, WES has become a more robust means of identifying rare genetic disorders, hereditary diseases, variants and mutations related to cancer, and even pharmacogenomics. Researchers and clinicians have turned most frequently towards WES to make distinctive and novel associations of genes to disease, conduct population genetics studies, and aid precision medicine; the ultimate goal is to match specific treatments to individual patients' unique genetic underpinnings. The diagnostic yield of WES has been highly valuable, especially in cases of undiagnosed genetic disorders that are insufficiently met with conventional diagnostic tests. Furthermore, the fields of bioinformatics and the computational analysis of large genomic datasets have improved the likelihood of WES interpretation and become more accessible as a whole; although there are still future challenges in terms of processing large amounts of data and differentiating pathogenic variants from benign variants. In perspective, WES has been developed.

COVID-19 IMPACT

Pandemic catalyzed a surge as scientists explored genetic factors influencing COVID-19

The global COVID-19 pandemic has been unprecedented and staggering, with the market experiencing higher-than-anticipated demand across all regions compared to pre-pandemic levels. The sudden market growth reflected by the rise in CAGR is attributable to the market’s growth and demand returning to pre-pandemic levels.

The Whole Exome Sequencing market has been affected by the COVID-19 pandemic in several ways. COVID-19 changed the demand and application process for WES. For instance, at the beginning of the pandemic, most research was focused on understanding SARS-CoV-2 and related infectious diseases. Consequently, projects that were unrelated to infectious diseases (exome sequencing) saw a slower uptake as laboratory operations and constraints due to supply constraints delayed many projects, while funding was shifted to more acute virology research. Interestingly, COVID-19 led to long-term growth as both researchers acknowledged the role of genetics in determining susceptibility for individuals reacting differently to COVID-19, and in light of the global interest to understand severe outcomes in patients (the pandemic leveraged people's interest in genomics with a non-infectious context). This also opened new avenues for WES beyond many current areas of clinical genomics to include population health and epidemiological aspects of research. At the same time, awareness of genomics and precision medicine spiked worldwide, which in tandem prompted governments and health systems to enhance investment in data and sequencing disease infrastructure. Discussion and approaches to decentralised and digital healthcare advanced as a response to the pandemic; this ultimately created more options and streamlined options when consumers engage in genomics tests geared toward individualised therapy. In the aftermath and results stemming from the COVID-19 pandemic, the Whole Exome Sequencing market has moved forward with a significant maturation phase and active growth.

LATEST TRENDS

Integration of artificial intelligence (AI) and machine learning (ML) tools to enhance performance

One of the newest trends in the Whole Exome Sequencing market is the use of artificial intelligence (AI) and machine learning (ML) to support the interpretation and analysis of sequencing data, which is changing the ways we extract insights about the genome and apply those insights in research and clinical settings. The large amount of data generated from WES was one of the main problems with using WES, since definitively categorising pathogenic variants versus benign polymorphisms was difficult; however, with AI tools, we can automate variant calling, prioritise clinically relevant mutations, and predict functional effects of novel mutations with a higher degree of accuracy and pace. This means that we can reduce the time it takes to make a diagnosis, improve overall efficiency, improve accuracy and standardisation and reduce human error and inter-laboratory variability. There is a clear shift towards using cloud-based genomic data storage and analysis platforms, which facilitate collaborative research, real-time sharing of data, and can integrate multi-omics datasets (e.g., proteomics and transcriptomics) with exome data. Having a rapidly evolving discipline as personalised medicine, we see greater use of AI-driven exome sequencing as a method to find actionable mutations, particularly in cancer genomics, and support targeted therapy decisions. This trend is also further supported by an increasing partnerships and collaborations (healthcare companies, sequencing companies, bioinformatics companies).

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WHOLE EXOME SEQUENCING MARKET SEGMENTATION

By Type

Based on Type, the global market can be categorized into Agilent HaloPlex, Agilent SureSelect, Agilent SureSelect QXT, Illumina TruSeq Exome, Roche Nimblegen SeqCap and MYcroarray MYbaits.

• Agilent HaloPlex: Agilent HaloPlex is a targeted enrichment solution with optimised library preparation and high-performance exome sequencing. It is designed for researchers who want to identify rare variants in human exomes while reducing the cost of sequencing. It is a hybridisation-based capture application that uses optimised probe design to achieve high specificity and uniform coverage. The workflow and short hands-on preparation time are a real advantage, particularly for small to medium laboratories that are looking for precision without the long turnaround time. In the WES market, HaloPlex is extensively adopted in oncology research, rare disease detection, and pharmacogenomics because of its sensitivity and reproducibility.

• Agilent SureSelect: Agilent SureSelect has quickly become one of the fastest-distributed exome sequencing kits in the world, known for its reliability, high capture efficiency, and the capability to cover both coding and harder-to-access areas of the genome. SureSelect allows scalable sequencing from clinical research applications to high-throughput genomic work, favoured by both academic institutions and biopharma companies alike. Extremely popular for the detection of clinically pertinent variants, it has been well characterised and performed strongly in Mendelian disease studies and biomarker discovery. With upgrades to the product ongoing, SureSelect has maintained itself as a primary solution in WES and drives a large portion of validated market share.

• Agilent SureSelect QXT: The SureSelect QXT is a faster version of Agilent’s SureSelect technology, intended to maintain the capture efficiency of the original layout while enabling faster workflow. It is optimised for laboratories and clinics that need quick turnarounds without worrying about data quality. Its notable advantage is the reduced hybridisation step, which reduces library prep time significantly, thereby allowing sequencing results to be generated more quickly. This makes it a preferred choice for clinical diagnostic settings and urgent genomic testing, such as oncology screening or critical rare disease cases.

• Illumina TruSeq Exome: Illumina’s TruSeq Exome has emerged as another leading competitor in the WES market owing to the supremacy of Illumina’s sequencing platforms with respect to other providers. TruSeq Exome is also recognised by researchers due to the accuracy, uniform coverage, and seamless compatibility with Illumina’s sequencing hardware, which holds an impressive grip on the worldwide sequencing market, as well as its ability to support large-scale studies around population genomics and association studies for complex diseases. TruSeq Exome is designed to be scalable to support high-throughput sequencing. In addition, TruSeq Exome is also cheaper than other rival providers, allowing researchers to use TruSeq Exome for high-volume sequencing projects. It is often favoured by researchers because of its consistency, especially for the detection of single-nucleotide variants (SNVs) and small insertions/deletions.

• Roche Nimblegen SeqCap: Roche NimbleGen’s SeqCap technology is centred on customizable, high-content exome capture, allowing for flexible panel design and sequencing for specific applications. This makes it particularly attractive to cancer researchers and rare disease discovery, where researchers may need specially designed probes that a good portion of focus on genes of interest. While Roche’s sequencing platform has a growing array of competitive choices, SeqCap remains a good option for researchers who need a custom sequencing solution. Its appeal also extends to specialised laboratories focused on translational medicine and new biomarker discovery.

• MYcroarray Mybaits: MYcroarray's MYbaits technology has created customizable capture kits at affordable sequencing options for smaller labs and research groups. The flexibility of MYbaits to create unique panels is particularly attractive compared to an exome kit, which is relatively standardised. As the MYbaits kit can have an evolutionary biology, microbiology, or human disease focus, the potential to enrich for a specific genomic region with efficiency allows WES (whole exome sequencing) to expand beyond standard human genomics applications (which work best for diagnostic purposes), but also to comparative genomics and experimental model organisms. This ability for customisation has placed MYbaits in a unique position in academic research and individualised avenues of work.

By Application

Based on application, the global market can be categorized into Correlation Research of Normal Human, Mendelian Disease and Rare Syndrome Gene Discovery, The Research of Complex Diseases and Mouse Exome Sequencing.

• Correlation Research of Normal Human: WES, in this application, is used to characterize genetic variations in normal human populations to ask questions about evolutionary biology, population genetics, and phenotypic variation in relation to genetic variation. In human genetics, researchers often use WES to establish baseline exome profiles as reference for studies comparing diseased individuals. This element of WES also plays an important role in large population genome projects such as the 1000 Genomes Project, and with population biobanks, where WES assists in establishing large genomic databases to facilitate the development of personalized medicine and predictive health models.

• Mendelian Disease and Rare Syndrome Gene Discovery: A primary use of WES is the identification of genetic mutations associated with Mendelian disorders and rare syndromes. Because most of these disorders are caused by mutations in the protein-coding regions of the genome, WES is a more cost-effective and research-efficient diagnostic approach. Clinical research and clinical genetic counselling employ exome sequencing technologies to identify disease-causing genetic variants, and they are steadily enhancing diagnostic yield rates for such genetic conditions that previously did not have a diagnosis with non-genetic tools. This segment is set for considerable growth, thanks to heightened awareness of rare diseases, expansion of the domain by government-funded research, and the incorporation of genetic testing into clinically accepted medical practice.

• The Research of Complex Diseases: WES is an essential component for analysing polygenic and multifactorial diseases such as cancer, diabetes, cardiovascular disease, and neurological disease. With atypical Mendelian disorders, several genetic and environmental factors can determine the exposure to the disease. WES permits the discoverability of susceptibility genes, novel biomarkers, and therapeutic targets, and facilitates progress in precision medicine and drug development. This segment takes the highest market space due to the high prevalence of chronic diseases worldwide and the shift toward personalised healthcare.

• Mouse Exome Sequencing: WES is also used in research for model organisms, with mouse exome sequencing being one area of noted interest. Mice are very similar to humans on a genomic scale, and sequencing their exomes teaches us about gene function, disease modelling, some therapeutic testing, and many other biological areas. Scientists can use mouse exome data to understand the genetic components of human disease and to validate drug targets before human clinical trials. This application promotes translational research and expedites biomedical discovery mainly in oncology, neurobiology, and immunology.

MARKET DYNAMICS

Market dynamics include driving and restraining factors, opportunities and challenges stating the market conditions.

Driving Factors

Rising prevalence of genetic disorders boosts demand

One of the critical growth factors for the Whole Exome Sequencing market is the increasing frequency of genetic disorders and the demand for more complex diagnostic solutions to identify and provide answers to the root causes of patients' symptoms in a timely manner. Traditional, more widely accepted diagnostic strategies primarily rely on looking at a patient's symptoms, medical imaging, or testing one or two genes at a time, and it can sometimes be too little, or one often misses a rare or complex condition with multiple genetic causes. Whole Exome Sequencing reflexively solved that problem by providing a more comprehensive and cost-effective way to consider hundreds, or even thousands, of genes simultaneously, saving diagnostic time and increasing diagnostic yields for patients suspected to have rare Mendelian diseases or conditions associated with complex metabolic syndromes, developmental and congenital disorders, neurological illnesses, and the impact of environmental factors on health. The value of WES is magnified in the pediatric setting, where children with unexplained symptoms often undergo a series of evaluations, testing, or repeat testing, often referred to as the "diagnostic odyssey" and the semantic odyssey, which collectively do not necessarily yield answers. Reports show that WES could help to shorten the journey and eliminate unnecessary procedures, and directly inform treatment plans for the first time, ultimately saving healthcare costs or potentially improving health outcomes. Coupled with global precision medicine initiatives, WES was riding high with governments and healthcare systems alike, introducing guidelines and approaches for utilising reliable genetic testing to personalise and refine intervention and therapies to individuals. Patients, too, are becoming more aware and demanding a more personalised approach to their health, which creates additional demand for the use of WES, while government approval processes and facilitating greater access to WES contribute to a perfect storm of increasing consumer demand.

Rapid advancement of sequencing technologies has lowered costs and improved accuracy

Another important motivator of the Whole Exome Sequencing market has been the aggressive evolution of sequencing technologies and related bioinformatics tools that have reduced costs, increased accuracy, and improved availability at a population level. Over the last ten years, the cost of sequencing has been rapidly declining owing to innovations in next-generation sequencing technologies. This makes WES a viable option for many researchers and clinicians in a quasi-routine clinical practice setting, or for large-scale research projects. Improvements in capture kits, sequencing capacity, and error-corrected sequencing technologies have allowed technology developers to accurately execute sequencing within days of obtaining samples, and promise improved measures of accuracy for exome sequencing. Concurrent improvements in bioinformatics have derived sophisticated software pipelines to navigate massive datasets, filter for variants, and present such information in a user-friendly report format that can be digested by users with minimal genomic background. The increased availability of WES technology has also benefited from the adoption of cloud computing and AI-based analytics, making advanced sequencing and analyses accessible to smaller laboratories, hospitals, and research institutions without the associated burden of developing expensive in-house infrastructure. Finally, with the urgent pressures for pharmaceutical and biotechnology companies to discover therapeutic drugs and develop biomarkers for predictive modelling, WES is increasingly implemented for drug discovery and biomarker identification, such as in oncology or rare diseases, where summarising genetic insights can lead to faster precision drug development timelines. With better technology, newfound measures of reliability, and improved capacity to analyse larger datasets with high variability, WES is quickly evolving, and thus further fuelling a protein revolution.

Restraining Factor

High costs associated with sequencing and data interpretation limit its widespread adoption

The major inhibiting factor influencing the whole exome sequencing (WES) market is that genome sequencing, analysis, and data interpretation remain expensive, prohibiting widespread use, especially in developing areas and small healthcare systems. While the cost of sequencing whole genome/exome has drastically decreased in the past ten years, the total costs - including library prep, installation and maintenance of a sequencing platform, bioinformatics systems, data storage, and interpretation of genomic data by trained professionals - are still a significant cost. Many hospitals, diagnostic labs, and research entities have limited financial resources, which limit their ability to acquire WES. Additionally, abstracting from sequencing costs, WES requires budgets to purchase computational tools, bioinformatics expertise, investment in training, and to protect patient data obtained through sequencing. Also, health insurers have been hesitant to reimburse for WES-based diagnostics, especially where exploratory and not yet validated as a clinical service, thus increasing out-of-pocket expenditures for patients. This lack of reimbursement is also a barrier to market growth in places where questions of cost-effectiveness and demonstrated clinical utility are still being evaluated. Further, the complex data interpretation contributed to the slow adoption of WES by professionals, as a single test can yield tens of thousands of variants, the vast majority of which may have uncertain significance.

Scope of growth with the expanding application in personalised and precision medicine

Opportunity

Expand their programs in personalised and precision medicine, particularly in the area of oncology and rare diseases diagnostics, as an important opportunity in the whole exome market is growing. As the world increasingly invests efforts in precision medicine to give the best treatment based on personal genetic information, using WES is the most economical way of getting in-depth genetic information to decode protein-coding regions where disease-causing mutations are most likely to occur. The cancer care area represents one of the most significant growth areas of WES as oncologists continue to rely on genetic profiling information to make evidence-based opinions for targeted therapies, immunotherapies, and biomarker treatments. Given that WES can identify actionable mutations that can predict response or resistance to a drug, it creates real value by enhancing patient outcomes with a reduction in unnecessary treatment. In no way has the diagnosis of rare genetic disorders become a significant untapped opportunity in the whole exome market, as countless patients are subjected to years of misdiagnosis due to inadequate traditional genetic testing estimations.

WES represents a much superior genetic testing option to provide an overall better genetic evaluation resulting in less diagnostic odyssey that can result in more timely and specific intervention. Significantly, the fast evolution of clinical WES with artificial intelligence and cloud-based analytics will facilitate an enhanced level of reliance for clinicians with a quick and accurate report, and will only improve with utilisation. As governments and health systems more and more globally expand their programs in personalised medicine, particularly in the area of rare disease diagnostics, it is hard to fathom how, in a short time, WES will be commonplace with clinical consumerisation of all forms of diagnostic testing with accuracy and timeliness.

Issue of data interpretation directly affects its integration into routine medical practice

Challenge

One major barrier facing the whole exome sequencing market is that of data interpretation & clinical utility, which impacts the implementation of whole exome sequencing into routine medical care. In contrast to targeted gene panels, which interrogate a small selection of known genes related to specific conditions, whole exome sequencing generates a large volume of data, with many individuals having thousands of variants per individual. The key challenge is how to separate mutations which are clinically meaningful and have clinical implications from those that are benign or of unknown significance. In addition, there are challenges associated with the interpretations of many genetic variants due to limited databases & gaps in scientific knowledge, leading to ambiguity in the clinical context for decision-making.

In addition to clinical utility, there is the possibility of incidental findings, which are variations not related to the condition being tested, but may be relevant for other health conditions that the clinician must consider how and if they should communicate this information to the patient. Lack of standardisation in methodology and guidelines for the interpretation and reporting of whole exome sequencing across institutions and countries has further complicated its use, and raised questions about reproducibility and consistency of outcomes. In addition, as physician do not get any formal training in years of medical training on genomics, it is often a major challenge for them to incorporate whole exome sequencing findings into their treatment plan. This is against the context of needing more genomic training and potential cross-disciplinary group training.

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WHOLE EXOME SEQUENCING MARKET REGIONAL INSIGHTS

• North America

North America, and especially the United States Whole Exome Sequencing market, is the largest region in the whole exome sequencing (WES) market due to its very sophisticated health care system, advanced research ecosystem, and leading sequencing companies and research institutions pushing the field forward. The USA has a long history of piloting genomic research. For example, the US played a leading role in the Human Genome Project, and it also has a large number of ongoing large-scale projects, such as the NIH All of Us Research Program, to gather genomic and health information from over one million individuals to improve personalised medicine and population health. With established sequencing leaders in the US, such as Illumina, Thermo Fisher Scientific, and Agilent Technologies, there is an established domestic ecosystem allowing for access to emerging sequencing platforms and bioinformatics platforms with relative ease. It is important to consider the continued public and private funding supporting the uptake of WES into hospitals, diagnostic centres, and research institutions. For example, the US government has increased funding for genomic medicine and cancer research through federal initiatives such as the Cancer Moonshot, which has fast-tracked the use of exome sequencing in oncology to support biomarker discovery, optimising treatments, and companion diagnostics. The clinical implementation of WES is particularly strong in the U.S., where healthcare professionals are increasingly using it for diagnoses of rare diseases, inherited conditions, and pediatric genetic disorders, especially since their traditional approaches are generally not yielding satisfactory solutions. Additionally, the favourable regulatory environment has improved approval pathways within the U.S. Food and Drug Administration (FDA), allowing companies to gain approval for genomic diagnostics faster to market. Furthermore, collaborations among healthcare providers, biotech companies, and their pharmaceutical partners are reinforcing the ecosystem that includes WES for drug discovery processes, clinical trials, and patient stratification based on genetic variants.

• Europe

As for European Whole Exome Sequencing market share, it represents another key market for whole-exome sequencing, particularly noting a rapidly evolving genomics research space, significant government support, and active involvement of large studies in a number of significant universities and clinical and academic research organisations. In particular, the United Kingdom, Germany, France, and Nordic countries embrace futuristic genomics practices and have adopted WES in clinical, translational, and research realms. For instance, the United Kingdom's National Health Service (NHS), including the United Kingdom's Genomic Medicine (Genomics England) program, has been pivotal in increasing access to genomic medicine in the UK medical community through earlier initiatives like 100,000 Genomes Project, and then into more recent, operational activities to use genomic sequencing for clinical practice in cancer and rare diseases. Notably, Germany has committed significant public financing to precision medicine research and participated in both evaluation and partnerships in academic partnerships with private actors interested in implementing WES in oncology, cardiology, and rare disease diagnostics. The level of engagement by universities and research centres in genomics research is very high in Europe, often in partnerships with biotech or pharmaceutical firms to provide genomic studies into translational medicine and drug development. Even the European Union sees genomics in a significant way, subsequently encouraging funding bids, particularly within the Horizon Europe research framework, to ensure investment into both sequencing infrastructure and bioinformatics development support. Compared to North America, Europe presents a more complicated regulatory environment due to。

• Asia

The Asia-Pacific region, with an emphasis on countries including China, Japan, South Korea, and India, is being recognised as one of the fastest-growing markets for whole exome sequencing (WES), propelled by national advances in healthcare infrastructure, increased governmental investment into genomics, and the presence of cost-competitive sequencing providers. China is becoming a powerhouse in the Asia-Pacific region based on its large-scale population genomics projects, such as the China Precision Medicine Initiative, and due to the presence of BGI, a global sequencing company that currently offers rapid and cost-effective sequencing services (domestically and abroad). Japan is making significant strides with governmental initiatives geared towards precision medicine and the application of WES for cancer research, rare genetic diseases, and ageing conditions associated with its ageing population. Similarly, South Korea is utilising the Korean Genome Project, India is currently building a national genomic database through the Genome India Project, and both will create tremendous demand for WES for population-level studies and clinical applications. Cost-effective sequencing based on lowered operating costs, and by local companies with pricing that is entering the competitive space of Western markets, is a major opportunity for Asia. Furthermore, the burdens of additional genetic chronic diseases with policy changes now include more focus on the relationship between genetic and chronic disease patients. Continued inconsistency in the regulatory environments throughout Asia presents challenges, but countries such as Japan and South Korea are quickly establishing favourable regulations, while China is improving its oversight to emphasise quality and ethics in sequencing projects. Regardless of these regulatory impediments, the unique combination of large patient populations, government investment and support, cost-effectiveness, and a growing private sector investment in Asia-Pacific is making it the fastest-growing region in terms of WES, while projecting to compete with North America and Europe for adoption and revenue within the next decade. Asia is viewed as the dominant region in terms of future growth within the WES market and the region with the largest potential for new growth due to the rapid pace of growth across the region and its population genomics ambitions.

KEY INDUSTRY PLAYERS

Key Industry Players Shaping the Market Through Enhancing Data Analysis Capabilities

Play important roles to influence the progression and development of the whole exome sequencing market by advancing sequencing technology, improving capabilities for data analysis, and broadening the application of WES in clinical settings. Illumina and Thermo Fisher Scientific are market-leading suppliers of sequencing platforms, providing high throughput, accuracy, and low-cost options while investing heavily in software solutions around data management and analysis. Meanwhile, Qiagen and Agilent Technologies help solidify the whole sequencing ecosystem through their respective contributions in sample preparation and enrichment kits, as well as bioinformatics pipelines; as a result, making sequencing workflows more streamlined and available. BGI Genomics and Eurofins Scientific provide services to expand the access of WES by furnishing large-scale sequencing services to research institutions and health providers, and pricing their services competitively; consequently, accelerating adoption, outside North America, of WES. Ongoing efforts from many others, like Fulgent Genetic and Personalis, seek to transition WES into clinical practice with a focus on cancer genomics and the diagnosis of rare diseases, in an effort to connect the dots between the world of academic research and operational health sectors. Their efforts employ a variety of strategies, including partnerships with hospitals, collaborations with academic institutions, and participation in government-backed genomics programs; these actions only strengthen their position in the marketplace. Further still, these companies are integrating artificial intelligence and machine learning technology into their offerings to streamline data interpretation and reduce the bottlenecks associated with variant classification.

List Of Top Whole Exome Sequencing Companies      

• Illumina, Inc. (U.S.)
• Thermo Fisher Scientific, Inc. (U.S.)
• Agilent Technologies, Inc. (U.S.)
• Qiagen N.V. (Netherlands)
• BGI Genomics (China)
• Eurofins Scientific SE (Luxembourg)
• Fulgent Genetics (U.S.)
• Personalis, Inc. (U.S.)

KEY INDUSTRY DEVELOPMENT

March 2023: Illumina announced that it was releasing its NovaSeq X Series, a next-generation sequencing platform that has substantially reduced the cost to sequence and increased throughput, thus enabling large-scale whole exome and whole genome sequencing for research or clinical use. This will hasten the momentum of WES adoption for precision medicine and for population-scale genomics studies.

REPORT COVERAGE

The study encompasses a comprehensive SWOT analysis and provides insights into future developments within the market. It examines various factors that contribute to the growth of the market, exploring a wide range of market categories and potential applications that may impact its trajectory in the coming years. The analysis takes into account both current trends and historical turning points, providing a holistic understanding of the market's components and identifying potential areas for growth.

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