市場調查報告書
商品編碼
1494619
基因組測試市場:按組件、技術、應用、分銷管道、最終用途分類 - 2024-2030 年全球預測Genome Testing Market by Component (Consumables, Equipment, Software & Services), Technology (Microarrays, Next-Generation Sequencing, Targeted Sequencing), Application, Distribution Channel, End-use - Global Forecast 2024-2030 |
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預計2023年基因組檢測市場規模為175.7億美元,預計2024年將達到197.6億美元,2030年將達419億美元,複合年成長率為13.21%。
基因組測試通常稱為全基因組定序 (WGS),涉及一次性檢查生物體基因組中 DNA 的完整序列。這種全面的分析涵蓋了所有類型的遺傳變異,包括插入、缺失、單核苷酸多態性 (SNP)、拷貝數變異和大的結構變化。人們對早期疾病檢測和預防的日益關注,以及對血統和系譜日益成長的興趣,也增加了基因組測試的重要性。然而,與基因組設備相關的高成本和解釋遺傳訊息的複雜性正在影響市場成長。此外,人工智慧和巨量資料分析的結合以改善遺傳資料的解釋,正在為市場成長創造潛在機會。
主要市場統計 | |
---|---|
基準年[2023] | 175.7億美元 |
預計年份 [2024] | 197.6億美元 |
預測年份 [2030] | 419億美元 |
複合年成長率(%) | 13.21% |
區域洞察
在美洲,特別是在美國和加拿大,個人化醫療意識的增強以及對預防性醫療保健的興趣日益濃厚,正在推動消費者對基因組檢測的需求。在高可支配收入和大量醫療保健支出的推動下,這些地區的客戶表現出投資健康和保健的意願。遺傳疾病的日益普及正在推動對基因組檢測服務的需求。由於成員國之間醫療保健系統、法規和消費者態度的差異,歐盟 (EU) 為基因組檢測提供了多元化的市場。隱私權問題、道德考量以及一般資料保護規範 (GDPR) 等法規結構對客戶的購買行為有重大影響。中東和非洲新興國家對基因組檢測的需求程度不同。在中東,每個國家都擁有發達的醫療保健系統,人們對個人化醫療的基因組測試的興趣與日俱增。亞太地區基因組檢測市場正在迅速開拓,特別是在中國、日本和印度。中國對生物技術的投資正在迅速增加,大型基因組研究計劃和國際合作就是證明。
FPNV定位矩陣
FPNV定位矩陣對於評估基因組檢測市場供應商的市場定位至關重要。此矩陣提供了對供應商的全面評估,並檢驗了與商務策略和產品滿意度相關的關鍵指標。這種詳細的評估使用戶能夠根據自己的要求做出明智的決定。根據評估結果,供應商被分為代表其成功程度的四個像限:前沿(F)、探路者(P)、利基(N)和重要(V)。
市場佔有率分析
市場佔有率分析是一種綜合工具,可對基因組測試市場中供應商的現狀進行深入而詳細的評估。透過仔細比較和分析供應商的貢獻,您可以更深入地了解每個供應商的績效以及他們在爭奪市場佔有率時面臨的挑戰。這些貢獻包括整體收益、客戶群和其他重要指標。此外,該分析還提供了對該領域競爭性質的寶貴見解,包括在研究基準年觀察到的累積、分散主導地位和合併特徵等因素。有了這些詳細資訊,供應商可以做出更明智的決策並製定有效的策略,以在市場競爭中保持領先地位。
策略分析與建議
策略分析對於尋求在全球市場站穩腳跟的組織至關重要。對目前在基因組測試市場中的地位進行全面評估,使公司能夠做出符合其長期願望的明智決策。此關鍵評估涉及對組織的資源、能力和整體績效進行徹底分析,以確定核心優勢和需要改進的領域。
[199 Pages Report] The Genome Testing Market size was estimated at USD 17.57 billion in 2023 and expected to reach USD 19.76 billion in 2024, at a CAGR 13.21% to reach USD 41.90 billion by 2030.
Genome Testing, often referred to as whole genome sequencing (WGS), involves examining the complete sequence of DNA in an organism's genome at a single time. This comprehensive analysis covers all types of genetic variations, including insertions, deletions, single nucleotide polymorphisms (SNPs), copy number variations, and large structural changes. Growing emphasis on early disease detection & prevention, along with the increasing interest in ancestry and genealogy, boosts the significance of genome testing. However, the high cost associated with genomics equipment and the complexity of interpreting genetic information impact the market growth. Furthermore, the integration of AI and big data analytics for improved interpretation of genetic data is creating a potential opportunity for market growth.
KEY MARKET STATISTICS | |
---|---|
Base Year [2023] | USD 17.57 billion |
Estimated Year [2024] | USD 19.76 billion |
Forecast Year [2030] | USD 41.90 billion |
CAGR (%) | 13.21% |
Regional Insights
In the Americas, particularly in the United States and Canada, the consumer need for genome testing is driven by a heightened awareness of personalized medication and a growing focus on preventive healthcare procedures. Customers in these regions exhibit a willingness to invest in health and wellness, supported by higher disposable income and substantial healthcare spending. The increasing prevalence of genetic disorders has catalyzed the demand for genome testing services. The European Union displays a diverse market for genome testing due to differences in healthcare systems, regulations, and consumer attitudes across member countries. Privacy concerns, ethical considerations, and regulatory frameworks such as the General Data Protection Regulation (GDPR) profoundly influence customer purchasing behavior. Emerging economies in the MEA show varying levels of demand for genome testing. The Middle East, with its well-funded healthcare systems in countries, is witnessing an increased interest in genome testing for personalized medicine. The Asia Pacific region, especially China, Japan, and India, exhibits a rapidly developing market for genome testing. China's investment in biotechnology has soared, as evidenced by its large-scale genome research projects and international collaborations.
Market Insights
The market dynamics represent an ever-changing landscape of the Genome Testing Market by providing actionable insights into factors, including supply and demand levels. Accounting for these factors helps design strategies, make investments, and formulate developments to capitalize on future opportunities. In addition, these factors assist in avoiding potential pitfalls related to political, geographical, technical, social, and economic conditions, highlighting consumer behaviors and influencing manufacturing costs and purchasing decisions.
FPNV Positioning Matrix
The FPNV positioning matrix is essential in evaluating the market positioning of the vendors in the Genome Testing Market. This matrix offers a comprehensive assessment of vendors, examining critical metrics related to business strategy and product satisfaction. This in-depth assessment empowers users to make well-informed decisions aligned with their requirements. Based on the evaluation, the vendors are then categorized into four distinct quadrants representing varying levels of success, namely Forefront (F), Pathfinder (P), Niche (N), or Vital (V).
Market Share Analysis
The market share analysis is a comprehensive tool that provides an insightful and in-depth assessment of the current state of vendors in the Genome Testing Market. By meticulously comparing and analyzing vendor contributions, companies are offered a greater understanding of their performance and the challenges they face when competing for market share. These contributions include overall revenue, customer base, and other vital metrics. Additionally, this analysis provides valuable insights into the competitive nature of the sector, including factors such as accumulation, fragmentation dominance, and amalgamation traits observed over the base year period studied. With these illustrative details, vendors can make more informed decisions and devise effective strategies to gain a competitive edge in the market.
Recent Developments
Cone Health Readies for 100,000 Person Genomics Project
Cone Health is on the brink of launching an expansive genomic testing initiative designed to enhance the health and longevity of individuals throughout the Piedmont Triad region. The program aims to harness the predictive power of genomics to identify individuals at risk for certain diseases, such as breast cancer and cardiac issues, thereby enabling early intervention and personalized healthcare. Cone Health has partnered with population genomics specialist, Helix, and envisages recruiting 100,000 healthy volunteers within five years for DNA sequencing via blood or saliva samples. [Published On: 2023-12-04]
Illumina Launches Advanced Liquid Biopsy Assay to Enable Comprehensive Genomic Profiling of Solid Tumors
Illumina Inc. has unveiled its latest innovation, the TruSight Oncology 500 ctDNA v2 (TSO 500 ctDNA v2), designed for the comprehensive genomic profiling (CGP) of circulating tumor DNA (ctDNA) using a noninvasive liquid biopsy approach. The TSO 500 ctDNA v2 presents a significant advancement for cancer research, offering a viable solution for genomic profiling when tissue samples are unattainable or enhancing the insights gained from traditional tissue-based tests. [Published On: 2023-11-01]
Apollo Opens Genomic Institute In Chennai, to Open Three More in 2023
Apollo Hospitals Group has inaugurated a Genomics Institute in Chennai to advance the study of genes and tackle genetic disorders. This marks the newest addition to their growing network with existing facilities in Mumbai and Delhi. By the end of 2023, Apollo is poised to enhance its genomic footprint with additional institutes launching in Hyderabad, Bangalore, and Ahmedabad. The Chennai Institute is set to offer comprehensive genomic services, including genetic evaluation, clinical diagnostics, obstetric genetics, and cancer genomics. These services are meticulously designed to provide patients with critical information for the management and prevention of genetic disorders. [Published On: 2023-04-25]
Strategy Analysis & Recommendation
The strategic analysis is essential for organizations seeking a solid foothold in the global marketplace. Companies are better positioned to make informed decisions that align with their long-term aspirations by thoroughly evaluating their current standing in the Genome Testing Market. This critical assessment involves a thorough analysis of the organization's resources, capabilities, and overall performance to identify its core strengths and areas for improvement.
Key Company Profiles
The report delves into recent significant developments in the Genome Testing Market, highlighting leading vendors and their innovative profiles. These include 10x Genomics, 23andMe, Inc, Abbott Laboratories, Agilent Technologies, Inc., BGI Group, Bio-Rad Laboratories, Inc., Danaher Corporation, Eurofins Scientific SE, F. Hoffmann-La Roche, Ltd., Freenome Holdings, Inc., GeneDx, LLC, Genomic Testing Cooperative, Helix OpCo, LLC, Illumina, Inc., Merck KGaA, New England Biolabs, Inc., Novogene Co, Ltd., Oxford Nanopore Technologies PLC, PerkinElmer Inc., QIAGEN N.V., Quest Diagnostics Incorporated, Takara Bio Inc, Thermo Fisher Scientific Inc., Ultima Genomics, Inc., and VWR International, LLC.
Market Segmentation & Coverage