The Whole Exome Sequencing (WES) industry is dynamic, driven by technology, research, and genetic medicine. Genomic research, diagnostics, and customized medicine players must understand market dynamics.
Continuous WES technical advances drive market dynamics. Sequencing systems, bioinformatics tools, and data analysis algorithms improve accuracy, efficiency, and cost-effectiveness, pushing WES use in many applications.
Current R&D projects affect market dynamics. Academic institutions, biotechnology businesses, and pharmaceutical corporations invest in WES applications, disease-associated variation identification, and genetic medicine research.
Rising precision medicine demand affects market dynamics. WES helps discover disease-related genetic variations, allowing genomic-based therapy strategies. This follows the trend of genetically customizing healthcare.
The WES market is shifting toward clinical diagnostics and illness screening. WES enables early diagnosis, carrier screening, and informed family planning by detecting pathogenic variations associated to hereditary illnesses.
WES cost reduction and accessibility affect market dynamics. WES usage increases as technology makes it cheaper and more accessible, making genetic sequencing standard in healthcare.
Market dynamics include WES data integration with EHRs. Connecting genetic data to patient health records improves clinical decision-making, longitudinal investigations, and genomics incorporation into normal care.
Market dynamics recognize data interpretation and analysis issues. WES generates a lot of genomic data, requiring powerful bioinformatics tools for variant calling and analysis. These obstacles must be overcome to maximize WES data' therapeutic value.
Regulatory authorities determine clinical WES criteria, which affect market dynamics. The reliability and repeatability of WES outcomes depend on method standardization and regulatory compliance.
Market trends reflect WES's growing oncology use. WES is used to discover somatic mutations in cancer genomes, enable tailored medicines, predict therapy responses, and promote precision oncology.
Global collaborations and data-sharing affect market dynamics. International cooperation enable genomic data sharing, large-scale genomic investigations, and disease genetic component comprehension.
WES market dynamics emphasize genetic counseling and patient education. Comprehensive genetic counseling services help patients and healthcare professionals make genomic-based choices as WES becomes increasingly incorporated into clinical practice.
Competitive landscape and new technology affect market dynamics. Competition and innovation from new sequencing technology and varied market participants drive WES methodology developments.
WES market dynamics depend on ethics and data protection. Protecting patient privacy, obtaining informed consent, and resolving genetic information ethics promote WES patient confidence.
Whole Exome Sequencing Market Size was valued at USD 1.5 Billion in 2022. The Whole Exome Sequencing market industry is projected to grow from USD 1.8 Billion in 2023 to USD 7.8 Billion by 2032, exhibiting a compound annual growth rate (CAGR) of 20.20% during the forecast period (2023 - 2032). Increased use of whole-exome sequencing technology for various applications and research & development are the key market drivers enhancing market growth.
Source Secondary Research, Primary Research, MRFR Database and Analyst Review
Market CAGR for whole exome sequencing technology's various applications is driven by the rising number of chronic and rare disorders, the increasing need for customized treatment, and rising next–generation sequencing.  A method for sequencing a genome’s exome and protein-coding genes is called exome sequencing and whole exome sequencing. In this process, the subset of DNA that codes for proteins or exons is chosen, and the exonic DNA is then sequenced utilizing high-throughput DNA sequencing techniques. Additionally, it offers a low-cost screening method for the detection of genetic diseases. It offers a less resource-intensive substitute for whole-genome sequencing in several applications, including drug development processes.
The growing demand for identifying uncommon diseases, expanding genomics and next-generation sequencing R&D, and rising demand for personalized treatment drive the whole exome sequencing market. For Instance In March 2022, As per British Medical Journal article, routine whole exome sequencing for detecting rare children's genetic illnesses is now available for highly selected kids. According to the report, next-generation sequencing enables the rapid and inexpensive sequencing of hundreds or thousands of genes. The advantages of exome sequencing are factors expected to grow the market.
Testing for the genomes of viruses that cause diseases, such as HIV, Cancer, and Covid-19, involves whole exome sequencing. The need for whole exome sequencing is fast expanding along with the prevalence of these disorders. For instance the World Health Organization (WHO) announced in July 2022 that there were 37.7 million HIV cases worldwide in 2021. Due to the rise in these illnesses and the increased demand for RNA sequencing, these genomic sequencing techniques offer information on genetic variations that can cause diseases. Thus, driving the Whole Exome Sequencing market revenue.
The Whole Exome Sequencing market segmentation, based on product, includes kits, systems, and services. The system segment dominated the market, accounting for maximum market revenue. Next-Generation Sequencing (NGS) and data analysis services provided advanced bioinformatics visualization, allowing researchers to concentrate more on their work than laborious analysis operations. These sequence analysis services provide various services, such as library development from a wide range of samples, experimental planning, and downstream DNA sequence analysis.
The Whole Exome Sequencing market segmentation, based on technology, includes sequencing by synthesis (SBS) and ION semiconductor sequencing. The sequencing by synthesis (SBS) segment generated the most revenue. This technique eliminates mistakes and missed calls by repeating nucleotide strings. SBS technology offers long-insert paired-end reads for de novo sequencing, effective sequence assembly, and other uses, in addition to high-resolution genome sequencing, to short–insertpaired–end reads.
Figure 1 Whole Exome Sequencing Market, by Technology, 2022 & 2032 (USD Billion)
Source Secondary Research, Primary Research, MRFR Database and Analyst Review
The Whole Exome Sequencing market segmentation, based on application, includes diagnostics, drug discovery and developments, and agriculture and animal research. The drug discovery and development segment generated the maximum market revenue. Medical experts may create safer and more efficient treatment plans and drugs for various health disorders thanks to advancements in genetics. This drug discovery and development segment market is driven by the increase in the prevalence of different kinds of cancer, the affordability of personalized drug therapy, the high adoption in developed markets, and the development of novel drugs.
The Whole Exome Sequencing market segmentation, based on end-user, includes research centers and government institutes, hospitals and diagnostics centers, and pharmaceuticals & biotechnology companies. The research centers and government institutes category generated the most income. Research centers and government institutions have offered a clinical diagnosis of chronic diseases such as cardiovascular disorders, Alzheimer’s disease, cancer, and others. Moreover, R& D in the field of genomics is also supporting the segment's growth.
By region, the study provides market insights into North America, Europe, Asia-Pacific and Rest of the World. The North American Whole Exome Sequencing market will dominate this market, owing to an increase in hereditary and chronic diseases. In addition, the growing demand for targeted and personalized drugs will boost the market growth in this region.
Further, the major countries studied in the market report are The US, Canada, German, France, the UK, Italy, Spain, China, Japan, India, Australia, South Korea, and Brazil.
Figure 2 WHOLE EXOME SEQUENCING MARKET SHARE BY REGION 2022 (USD Billion)
Source Secondary Research, Primary Research, MRFR Database and Analyst Review
Europe's Whole Exome Sequencing market accounts for the second-largest market share due to the technological advancement in the field of genomics and the rise in R&D. Further, the German Whole Exome Sequencing market held the largest market share, and the UK Whole Exome Sequencing market the fastest growing market in the European region.
The Asia-Pacific Whole Exome Sequencing Market is expected to rise at the fastest CAGR from 2023 to 2032 due to the rising incidence of genetic abnormalities among people caused by increasing public knowledge of whole exome sequencing. Moreover, China’s Whole Exome Sequencing market held the largest market share, and the Indian Whole Exome Sequencing market was the fastest-growing market in the Asia-Pacific region.
Whole Exome Sequencing Key Market Players & Competitive Insights
Leading market players are investing heavily in research and development to expand their product lines, which will help the Whole Exome Sequencing market, grow even more. Market participants are also undertaking several strategic activities to expand their  footprint, with important market developments including new product launches, contractual agreements, mergers and acquisitions, higher investments, and collaboration with other organizations. The whole Exome Sequencing industry must offer cost-effective items to expand and survive in a more competitive and rising market climate.
Manufacturing locally to minimize operational costs is one of the key business tactics manufacturers use in the  Whole Exome Sequencing industry to benefit clients and increase the market sector. In recent years, the Whole Exome Sequencing industry has offered some of the most significant medical advantages. Major players in the Whole Exome Sequencing market, including Illumina Inc. (US), BGI (China), Eurofins Scientific (Belgium), Thermo Fisher Scientific (US), Agilent Technologies Inc. (US), F.Hoffmann-La Roche Ltd. (Switzerland), GENEWIZ (US), Ambry Genetics (US), Macrogen Inc. (South Korea), Integragen SA (France), and others, are attempting to increase market demand by investing in research and development operations.
Illumina, Inc. (America) is a biotechnology company headquartered in San Diego, California, and it aids more than 140 countries. Illumina, founded on April 1, 1998, creates, produces, and sells integrated systems to study genetic variation and biological function. The business offers a selection of goods and services to cater to the markets for sequencing, genotyping and gene expression, and proteomics. For Instance in February 2023, as per Illumina Inc., the Broad Institute received the first NovaSeqX Plus Machine. The platform will assist parties wishing to access the company’s human whole genome product, lent genome/exome product, and sequencing service.
NanoString Technologies, Inc. is a publicly traded biotech company providing discovery and translation research solutions. The nCounter® Gene Expression System, the GeoMx® Digital Spatial Profiler, the CosMxTM Spatial Molecular Imager, and the AtoMX Spatial Informatics Platform are among the products made by NanoString. With the help of these four systems, researchers may see molecular interactions in three dimensions and understand how genes and proteins are expressed on a multi-genomic level about tissue shape. Products made by NanoString are based on a cutting-edge digital molecular barcoding technique developed at the Institute for Systems Biology by Dr. Leroy Hood. For Instance In May 2022, NanoString Tehnologies, Inc. released a cloud-based process that benefits users of the GeoMx Digital Spatial Profiler and Illumina NextSeq 1000 and NextSeq 2000 sequencing devices.
Key Companies in the Whole Exome Sequencing market include
Whole Exome Sequencing Industry Developments
May 2022Â Thermo Fisher Scientific and the Qatar Genome Program (QGP), a division of the Qatar Foundation (QF), come together for advancing genomic studies and therapeutic uses of predictive genomics in Qatar.
February 2021Â Labcorp and OmniSeq, a CAP-accredited molecular diagnostic innovation of Rosewell Park Comprehensive Cancer Center, released the launch of OmniSeq INSIGHTsm, a thorough genomic and immunological profiling tissue-based test that incorporates Next Generation Sequencing (NGS) technology. OmniSeq is a CAP-accredited molecular diagnostic invention of Rosewell Park Comprehensive Cancer Center.
© 2024 Market Research Future ® (Part of WantStats Reasearch And Media Pvt. Ltd.)