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Whole Exome Sequencing Market Analysis

ID: MRFR//7291-CR | 164 Pages | Author: Kinjoll Dey| May 2020

Whole Exome Sequencing Market Deep Dive โ€“ PESTLE, Porter, SWOT

The whole-exome sequencing (WES) market is expected to play a significant role in the evolution of genomic medicine, driven by technological advancements and the growing demand for personalized medicine. As a result of the increasing recognition of the importance of exome analysis in the understanding of genetic disorders, the demand for WES is set to increase. The market is characterized by the diversity of its applications, such as rare disease diagnosis, cancer genomics and pharmacogenomics, and the increasing use of bioinformatics tools to enhance data interpretation. The rise of academic-industrial collaborations is also fostering innovation and increasing the accessibility of WES, thus attracting a broader range of stakeholders. The WES market is at the forefront of the transformation of medicine, enabling comprehensive insights into the genetic causes of diseases.

PESTLE Analysis

  • Political:
    In 2025, governments are increasingly supportive of the development of genomics and personalised medicine. Over thirty countries have set up national genomics initiatives. In the United States, for example, the National Institutes of Health allocated $US1 billion to research on human genetics in 2024, and is expected to allocate similar sums in 2025. In the United Kingdom, the Medical Research Council has set up a ยฃ600 million fund. This kind of political support is vital for the development of whole exome sequencing. It encourages collaboration between public institutions and private companies, which in turn fosters innovation and makes WES widely available.
  • Economic:
    The economic outlook for exome-based screening is positive because of the rising demand for genetic testing. The worldwide market for genetic testing services is expected to reach $20 billion by 2025. And the cost of exome screening is expected to drop to approximately $1000 per test by 2024, making it more affordable for both patients and physicians. The lower cost of exome screening will drive higher uptake rates, especially in emerging markets, where spending on health care is rising.
  • Social:
    Surveys show that in the developed countries over seventy per cent of people are willing to undergo genetic testing for the purpose of obtaining information about their health. By the end of 2024, about sixty per cent of health-care professionals reported an increase in the number of patients who had asked about the possibility of genetic testing. This reflected a growing tendency among the public to adopt a more preventive approach to health-care. This tendency was expected to continue into 2025 as educational campaigns and success stories helped to normalize the use of exome and genome sequencing in clinical practice.
  • Technological:
    Advances in exome-sequencing technology are driving the whole exome-sequencing market. The average time it takes to get the results of a whole exome-sequencing test is expected to be less than 2 weeks by 2025, thanks to advances in sequencing platforms and bioinformatics tools. In 2024, companies like Illumina and Thermo Fisher Scientific spent more than $500 million on R&D to improve the accuracy and efficiency of exome-sequencing. As a result, the quality of exome data available to scientists and clinicians is expected to improve significantly.
  • Legal:
    The legal framework of genetic research is being reorganized and new regulations are being introduced to ensure the protection of patient data and the ethical principles of the profession. In 2024, the European Union adapted the General Data Protection Regulation to include genetic data. The regulation requires explicit consent for the use of data and imposes a fine of up to 20 million on those who violate it. The stricter the legal framework, the more the companies operating in the whole exome market will have to change their practices to ensure compliance with the law and the trust of the public.
  • Environmental:
    Increasingly, the exome-sequencing market is being influenced by the question of the environment, especially with regard to the question of the long-term viability of laboratory practices. In 2024, approximately 40 per cent of laboratories said they had implemented green measures to reduce waste and energy consumption. By 2025, it is expected that at least 25 per cent of laboratories will have introduced greener technologies such as energy-efficient sequencers and waste-recycling programmes in response to growing concerns about the environment and the growing regulatory pressure to reduce the carbon footprint of health-care practices.

Porters Five Forces

  • Threat of New Entrants:
    Whole exome sequenc ing market - the medium market has significant capital and advanced technical knowledge, which limits the entry of new players. However, with the growing demand for personal medicine and the development of whole exome sequencing technology, new entrants may appear, resulting in a moderate level of competition.
  • Bargaining Power of Suppliers:
    Suppliers to the exome sequencing market, such as those providing reagents and platforms, have relatively low bargaining power. The market is dominated by a few large companies that can negotiate advantageous terms, and alternative suppliers are readily available.
  • Bargaining Power of Buyers:
    Buying Power of the Market: High - The buyers of the whole exome sequencing market, mainly research institutions and health care facilities, have a high negotiating power due to the availability of a large number of options and suppliers. In the long term, as buyers become more informed and more sensitive to price, they will be able to demand higher prices and bargain more effectively with suppliers.
  • Threat of Substitutes:
    There are other ways of testing for genetic abnormalities, such as targeted sequencing and whole-genome sequencing, but the unique advantages of whole-exome sequencing in providing a complete overview of the gene-coding regions lead to a medium risk. However, advances in substitutes could lead to a higher risk in the future.
  • Competitive Rivalry:
    Competition is high in the exome sequencing market. The market is highly competitive, with many established and new entrants competing for market share. The increasing number of exome-sequencing applications and the rapid evolution of the underlying technology have intensified the competition between the companies.

SWOT Analysis

  • Strengths:
    • High accuracy in identifying genetic variations linked to diseases.
    • Growing demand for personalized medicine and targeted therapies.
    • Advancements in sequencing technology leading to reduced costs and faster results.
  • Weaknesses:
    • High initial investment required for sequencing equipment.
    • Complex data interpretation requiring specialized skills.
    • Limited reimbursement policies for exome sequencing tests.
  • Opportunities:
    • Increasing prevalence of genetic disorders driving market growth.
    • Expansion of research initiatives in genomics and precision medicine.
    • Potential for integration with artificial intelligence for enhanced data analysis.
  • Threats:
    • Regulatory challenges and ethical concerns surrounding genetic data.
    • Intense competition from alternative genomic sequencing technologies.
    • Potential data privacy issues affecting consumer trust.

By 2025, the Whole Exome Sequencing Market is characterized by the advantages of high accuracy and the demand for individualized medicine, and the disadvantages of high cost and difficult data analysis. Opportunities will arise with the rise of genetic diseases and the development of technology, while threats will arise from the impact of regulatory policies and competition. Strategically, focusing on the improvement of access and the consideration of ethical issues will be the main trend of the market.

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