Global Whole Exome Sequencing Market

Global Whole Exome Sequencing Market Size, Share, Growth Analysis, By Technology(Targeted Sequencing, Whole Exome Sequencing and Others), By Application(Oncology, Rare Diseases), By End-user(Research Centers and Academic Institutions, Hospitals and Clinics) - Industry Forecast 2024-2031


Report ID: SQMIG35H2119 | Region: Global | Published Date: February, 2024
Pages: 157 | Tables: 92 | Figures: 76

Global Whole Exome Sequencing Market News

  • In July 2023, Roche and 23andMe announced a collaboration to develop a new DNA sequencing-based test to identify genetic variants associated with increased risk of hereditary cancers.
  • In May 2023, Thermo Fisher Scientific acquired Element Genomics, a company focused on leveraging CRISPR technology for functional genomics research, to strengthen its genomics portfolio.
  • In March 2023, Illumina and QIAGEN entered into a partnership to co-develop next-generation sequencing-based in vitro diagnostic (IVD) kits for oncology applications, aiming to enhance cancer diagnostics.
  • In January 2023, Agilent Technologies announced the launch of the Agilent Bravo 2.0 Automated Liquid Handling Platform, designed to streamline and automate genomic workflows in research laboratories.
  • In September 2022, Genentech announced a collaboration with Adaptive Biotechnologies to develop personalized neoantigen-based vaccines for the treatment of solid tumors.
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Whole Exome Sequencing Market size was valued at USD 360.02 million in 2021 and is poised to grow from USD 422.95 million in 2022 to USD 1534.62 million by 2030, growing at a CAGR of 17.48% during the forecast period (2023-2030).

The global whole exome sequencing market is characterized by the presence of various companies offering sequencing platforms, reagents, and analysis software. These companies strive to differentiate themselves by providing innovative and cost-effective solutions to meet the growing demand for whole exome sequencing. Market players focus on research and development activities to enhance their product portfolios and expand their customer base. Additionally, partnerships, collaborations, and acquisitions are common strategies employed by companies to strengthen their market position and gain a competitive edge. The competitive landscape is dynamic, with new entrants continuously emerging and established players seeking to maintain their market share. 'Illumina (US)', 'Thermo Fisher Scientific (US)', 'BGI Genomics (China)', 'Agilent Technologies (US)', 'Qiagen N.V. (Netherlands)', 'PerkinElmer (US)', 'Eurofins Scientific (Luxembourg)', 'Macrogen (South Korea)', 'Oxford Nanopore Technologies (UK)', 'Pacific Biosciences (US)', 'F. Hoffmann-La Roche AG (Switzerland)', 'GATC Biotech AG (Germany)', 'Genomatix GmbH (Germany)', 'ArcherDX, Inc. (US)', 'Foundation Medicine, Inc. (US)', 'Myriad Genetics, Inc. (US)', 'GeneDx (US)', 'Novogene Corporation (China)', 'Ambry Genetics (US)', 'Illumina Cambridge Ltd. (UK)'

One major driver propelling the growth of the whole exome sequencing market is the increasing demand for personalized medicine. The ability to study an individual's whole exome allows medical professionals to customize treatment plans based on the patient's unique genetic makeup and disease susceptibility. This personalized approach to healthcare offers the potential for more effective and targeted therapies, leading to improved patient outcomes. With advancements in sequencing technologies and data analysis tools, whole exome sequencing has become more accessible and affordable, further driving its adoption in clinical settings. The growing recognition of the value of personalized care is fueling the demand for whole exome sequencing and shaping the future of healthcare.

Integration of artificial intelligence (AI) and machine learning (ML) algorithms: One key market trend in the whole exome sequencing market is the integration of artificial intelligence (AI) and machine learning (ML) algorithms in data analysis and interpretation. AI and ML technologies are being leveraged to handle the large volumes of genomic data generated by whole exome sequencing and to identify meaningful patterns, genetic variations, and disease associations. These advanced analytical tools can assist in automating data processing, improving accuracy, and enhancing the efficiency of genomic analysis. By enabling faster and more accurate identification of genetic variants, AI and ML have the potential to revolutionize the field of whole exome sequencing, facilitating more precise diagnoses, personalized treatments, and advancements in genomic medicine.

The dominating region in the whole exome sequencing market is North America. This region has been at the forefront of technological advancements and has a well-established healthcare infrastructure, which has contributed to its dominance. In North America, the United States in particular has witnessed significant adoption of whole exome sequencing technology in both research and clinical settings. The presence of major key players, academic institutions, and research organizations focused on genomics research has further fueled the market growth in this region. Additionally, favorable government initiatives and funding for genomic research and precision medicine have played a crucial role in the dominance of North America in the whole exome sequencing market.

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Global Whole Exome Sequencing Market

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