查看購物車
  • Simplified Chinese
  • English
  • Japanese
  • Korean
封面
市場調查報告書
商品編碼
1597313

全基因組和外顯子定序市場 - 全球產業規模、佔有率、趨勢、機會和預測，按產品、工作流程、應用、最終用戶、地區和競爭細分，2019-2029F

Whole Genome and Exome Sequencing Market - Global Industry Size, Share, Trends, Opportunity, and Forecast, Segmented By Product, By Workflow, By Application, By End User, By Region and Competition, 2019-2029F
出版日期: | 出版商: TechSci Research | 英文 183 Pages | 商品交期: 2-3個工作天內

價格

We offer 8 hour analyst time for an additional research. Please contact us for the details.

簡介目錄

2023年全球全基因組和外顯子定序市場價值為19.1億美元，預計2029年將達到40.1億美元，預測期內複合年成長率為13.32%。

市場概況
預測期 2025-2029
2023 年市場規模 19.1億美元
2029 年市場規模 40.1億美元
2024-2029 年複合年成長率 13.32%
成長最快的細分市場 儀器儀表
最大的市場 北美洲

在基因組研究的進步、精準醫學的採用增加以及測序成本降低的推動下，全球全基因組和外顯子組測序市場正在經歷顯著成長。全基因組定序 (WGS) 可對整個基因組進行全面分析，而全外顯子定序 (WES) 則著重於蛋白質編碼區域，該區域約佔基因組的 1%，但與大多數遺傳疾病有關。這些技術對於識別罕見遺傳性疾病、癌症突變和遺傳性疾病至關重要，推動了醫療保健、學術和藥物研究領域的需求。

定序技術在臨床診斷和個人化醫療中的整合是一個關鍵的市場驅動力。世界各地的政府和私人組織正在增加對基因組研究的投資，以解決未滿足的醫療需求。例如，根據世界衛生組織 (WHO) 的愛滋病毒統計數據，到 2023 年，全球約有 3,990 萬人感染愛滋病毒。技術進步，包括下一代定序（NGS）平台、生物資訊學工具和基於雲端的資料分析，提高了定序服務的效率和可及性。直接面對消費者的基因檢測試劑盒的可用性不斷增加，進一步擴大了市場範圍。然而，道德問題、資料隱私問題和高昂的初始設定成本等挑戰可能會阻礙成長。隨著基因組定序變得更加經濟實惠且其應用多樣化，該市場有望在醫療保健和生命科學領域發揮變革性作用，在全球範圍內促進創新並改善患者的治療結果。

主要市場促進因素

精準醫療的採用率不斷提高

降低定序成本創造市場機會

下一代定序技術的進步

主要市場挑戰

測序基礎設施的初始成本高昂

資料隱私和道德問題

主要市場趨勢

臨床應用的擴展

政府和私人對基因組學的投資不斷增加

細分市場洞察

產品洞察

應用洞察

區域洞察

目錄

第 1 章：產品概述

第 2 章：研究方法

第 3 章：執行摘要

第 4 章：客戶之聲

第 5 章：全球全基因組與外顯子定序市場展望

  • 市場規模及預測
    • 按價值
  • 市佔率及預測
    • 按產品（套件、儀器）
    • 按應用（全基因組定序（腫瘤學、微生物、非侵入性產前檢測 (NIPT) 等）、全外顯子定序（腫瘤學、罕見疾病、基因發現等））
    • 按最終用戶（製藥和生物技術公司、診斷實驗室、醫院和診所、研究和學術機構等）
    • 按公司分類 (2023)
    • 按地區
  • 市場地圖

第 6 章：北美全基因組與外顯子定序市場展望

  • 市場規模及預測
    • 按價值
  • 市佔率及預測
    • 按產品分類
    • 按申請
    • 按最終用戶
    • 按國家/地區
  • 北美：國家分析
    • 美國
    • 墨西哥
    • 加拿大

第 7 章：歐洲全基因組與外顯子定序市場展望

  • 市場規模及預測
    • 按價值
  • 市佔率及預測
    • 按產品分類
    • 按申請
    • 按最終用戶
    • 按國家/地區
  • 歐洲：國家分析
    • 法國
    • 德國
    • 英國
    • 義大利
    • 西班牙

第 8 章：亞太地區全基因組與外顯子定序市場展望

  • 市場規模及預測
    • 按價值
  • 市佔率及預測
    • 按產品分類
    • 按申請
    • 按最終用戶
    • 按國家/地區
  • 亞太地區：國家分析
    • 中國
    • 印度
    • 韓國
    • 日本
    • 澳洲

第 9 章：南美洲全基因組與外顯子定序市場展望

  • 市場規模及預測
    • 按價值
  • 市佔率及預測
    • 按產品分類
    • 按申請
    • 按最終用戶
    • 按國家/地區
  • 南美洲：國家分析
    • 巴西
    • 阿根廷
    • 哥倫比亞

第 10 章：中東和非洲全基因組和外顯子定序市場展望

  • 市場規模及預測
    • 按價值
  • 市佔率及預測
    • 按產品分類
    • 按申請
    • 按最終用戶
    • 按國家/地區
  • MEA：國家分析
    • 南非
    • 沙烏地阿拉伯
    • 阿拉伯聯合大公國

第 11 章：市場動態

  • 促進要素
  • 挑戰

第 12 章：市場趨勢與發展

  • 併購（如有）
  • 產品發布（如有）
  • 最新動態

第 13 章：波特五力分析

  • 產業競爭
  • 新進入者的潛力
  • 供應商的力量
  • 客戶的力量
  • 替代產品的威脅

第14章：競爭格局

  • Agilent Technologies, Inc.
  • Thermo Fisher Scientific, Inc.
  • Bio-Rad Laboratories, Inc.
  • Eurofins Scientific SE
  • F. Hoffmann-La Roche Ltd
  • Illumina, Inc.
  • Laboratory Corporation of America Holdings
  • Novogene Corporation
  • Pacific Biosciences of California, Inc.
  • QIAGEN NV

第 15 章：策略建議

第16章調查會社について,免責事項

簡介目錄
Product Code: 26562

Global Whole Genome and Exome Sequencing Market was valued at USD 1.91 Billion in 2023 and is expected to reach USD 4.01 Billion by 2029 with a CAGR of 13.32% during the forecast period.

Market Overview
Forecast Period2025-2029
Market Size 2023USD 1.91 Billion
Market Size 2029USD 4.01 Billion
CAGR 2024-202913.32%
Fastest Growing SegmentInstruments
Largest MarketNorth America

The Global Whole Genome and Exome Sequencing Market is experiencing significant growth, driven by advancements in genomic research, increased adoption of precision medicine, and decreasing sequencing costs. Whole genome sequencing (WGS) offers a comprehensive analysis of the entire genome, while whole exome sequencing (WES) focuses on the protein-coding regions, which comprise approximately 1% of the genome but are linked to the majority of genetic diseases. These technologies are pivotal in identifying rare genetic disorders, cancer mutations, and inherited diseases, propelling their demand across healthcare, academic, and pharmaceutical research sectors.

The integration of sequencing technologies in clinical diagnostics and personalized medicine is a key market driver. Governments and private organizations worldwide are increasing investments in genomic research to address unmet medical needs. For instance, According to the World Health Organization (WHO) HIV Statistics, approximately 39.9 million individuals worldwide were living with HIV in 2023. Collaborations between technology providers and biopharmaceutical companies are accelerating the development of targeted therapies. Technological advancements, including next-generation sequencing (NGS) platforms, bioinformatics tools, and cloud-based data analysis, enhance the efficiency and accessibility of sequencing services. The increasing availability of direct-to-consumer genetic testing kits further expands market reach. However, challenges such as ethical concerns, data privacy issues, and high initial setup costs may hinder growth. As genomic sequencing becomes more affordable and its applications diversify, the market is poised to play a transformative role in healthcare and life sciences, fostering innovation and improving patient outcomes globally.

Key Market Drivers

Increasing Adoption of Precision Medicine

The increasing adoption of precision medicine significantly propels the growth of the Global Whole Genome and Exome Sequencing Market. Precision medicine customizes healthcare solutions based on individual genetic profiles, offering precise diagnoses, tailored treatments, and better patient outcomes. Whole genome sequencing (WGS) and whole exome sequencing (WES) play pivotal roles in this approach by uncovering specific genetic mutations and biomarkers essential for personalized treatment strategies. For example, WGS can identify rare genetic mutations that inform treatment options for complex conditions such as cancer, cardiovascular diseases, or rare genetic disorders, ensuring a more targeted therapeutic approach. This shift is further bolstered by robust government initiatives and private sector investments aimed at integrating genomic technologies into routine clinical care.

In addition to transforming patient care, precision medicine is revolutionizing the pharmaceutical industry. Genomic sequencing data enables pharmaceutical companies to refine drug development processes by identifying genetic markers that help pinpoint target populations.For instance, In March 2024, MGI Tech, a company dedicated to developing cutting-edge tools and technologies to advance life sciences, announced a significant collaboration with Eurofins Genomics Europe Genotyping A/S ("Eurofins Genomics"). Eurofins Genomics has placed a corporate order for the innovative DNBSEQ-T20X2 ("T20") ultra-high throughput sequencer, along with the ZTRON Appliance genomics data center and a suite of MGI's advanced laboratory automation products and systems. This order represents the first corporate purchase of the T20 in Europe, marking a notable step forward in the region's precision health initiatives. This approach enhances drug efficacy, reduces adverse reactions, and minimizes the likelihood of clinical trial failures, ultimately saving time and resources. The integration of genomic data into research and development processes is creating new opportunities for innovation in therapeutics.

The growing accessibility and affordability of WGS and WES have also stimulated collaborations among sequencing providers, pharmaceutical companies, and research institutions. These partnerships aim to leverage genomic data for breakthrough discoveries, resulting in an expanding application of genomic sequencing in precision medicine. The advent of advanced sequencing technologies and the increasing adoption of artificial intelligence and machine learning in genomic data analysis further amplify the potential of WGS and WES in clinical settings. As the healthcare landscape continues to embrace personalized treatment paradigms, the reliance on genomic sequencing technologies is expected to grow exponentially. Consequently, the integration of WGS and WES into precision medicine workflows positions these technologies as essential tools in advancing global healthcare, thereby driving substantial market growth.

Decreasing Sequencing Costs Creating Market Opportunities

The decreasing costs of sequencing have been a pivotal driver in expanding the adoption of Whole Genome Sequencing (WGS) and Whole Exome Sequencing (WES) technologies, significantly contributing to the growth of the global market. Over the past two decades, technological advancements in next-generation sequencing (NGS) platforms have dramatically reduced the cost of sequencing a human genome and this sharp decline has made genomic sequencing more accessible across diverse fields, enabling its application in clinical diagnostics, academic research, agriculture, and beyond.

In clinical settings, reduced sequencing costs have fostered the integration of genomic technologies into routine healthcare practices. Applications such as newborn screening, cancer diagnostics, and rare disease detection now commonly utilize WGS and WES due to their affordability and precision. This affordability allows healthcare providers to offer more personalized diagnostic and treatment solutions, improving patient outcomes while reducing overall healthcare costs. The ability to sequence at lower costs has spurred innovation in precision medicine, allowing researchers and clinicians to explore genetic markers more comprehensively.

The declining costs have also catalyzed the growth of direct-to-consumer genetic testing services, which heavily rely on WGS and WES technologies. Companies such as 23andMe, Ancestry, and others have leveraged the affordability of sequencing to offer accessible and cost-effective genetic testing kits, significantly broadening their customer base. These services not only provide consumers with health insights but also fuel demand for sequencing technologies. Beyond healthcare, affordable sequencing is transforming academic research and agriculture. Researchers can now conduct large-scale genomic studies, driving breakthroughs in genetic research, while agricultural genomics benefits from precise crop and livestock improvement initiatives.

Advances in Next-Generation Sequencing Technologies

Advances in next-generation sequencing (NGS) technologies have revolutionized the Global Whole Genome and Exome Sequencing Market, driving growth through enhanced speed, precision, and scalability. Modern NGS platforms are capable of processing massive volumes of genetic data with unprecedented efficiency, enabling comprehensive analyses that were previously unattainable. These platforms support a range of applications, from basic research to clinical diagnostics, making genomic sequencing an indispensable tool in modern science and medicine. Key innovations such as single-cell sequencing and long-read sequencing have further expanded the utility of NGS technologies. Single-cell sequencing enables the examination of genetic material at the resolution of individual cells, uncovering intricate details about cellular diversity, gene expression patterns, and disease mechanisms. Long-read sequencing, on the other hand, offers the ability to sequence longer DNA fragments, improving the accuracy of detecting structural variants and complex genomic regions. These advancements are particularly valuable for understanding rare genetic disorders, cancer genomics, and evolutionary biology.

The emergence of portable, user-friendly sequencing devices has also transformed the landscape of genomic research and clinical applications. Devices such as handheld sequencers allow smaller laboratories and field researchers to conduct genomic analyses without the need for extensive infrastructure. This democratization of sequencing capabilities has extended the reach of WGS and WES into diverse settings, including remote areas, wildlife research, and on-site clinical diagnostics. Portable sequencers have proven especially useful in emergency medical situations, such as outbreak investigations, where rapid genomic analysis is critical.

Advancements in NGS technologies have significantly reduced sequencing costs while increasing throughput, making WGS and WES more accessible for routine use. Faster turnaround times and improved automation have further streamlined workflows, enabling healthcare providers and researchers to deliver timely and accurate results.

Key Market Challenges

High Initial Costs of Sequencing Infrastructure

One of the primary challenges facing the Global Whole Genome and Exome Sequencing Market is the high initial cost associated with sequencing infrastructure. Although the cost per genome has significantly decreased over the past decade, the initial investment required to acquire advanced next-generation sequencing (NGS) machines and bioinformatics platforms remains substantial. Laboratories, especially smaller or newly established ones, may find it difficult to absorb these upfront expenses. The cost of not only sequencing equipment but also maintenance, reagents, consumables, and skilled personnel can be prohibitive, particularly in regions with limited healthcare budgets.

Sequencing infrastructure also requires substantial investment in data storage and computational power. WGS and WES generate massive amounts of data, and managing this data necessitates significant IT infrastructure, including secure cloud storage systems, high-performance computing resources, and data analytics platforms. The ongoing costs associated with these requirements add an additional layer of financial burden, especially for academic institutions and healthcare providers working with tight budgets. For these reasons, while the technology has become more affordable, the overall expense of integrating WGS and WES into clinical practice or research environments remains a key challenge. The cost burden is not only a barrier to widespread adoption but also hinders the scaling of sequencing operations in underserved regions, where healthcare infrastructure may already be strained.

Data Privacy and Ethical Concerns

As genomic sequencing generates vast amounts of sensitive data, data privacy and ethical concerns represent significant challenges for the Global Whole Genome and Exome Sequencing Market. The collection, storage, and use of genetic data raise issues related to consent, ownership, and confidentiality, particularly when it involves personal or familial health information. Informed consent is crucial in genomic testing, and patients must fully understand how their genetic data will be used, shared, and stored. There are concerns about how genetic data is stored and shared among research institutions, healthcare providers, and commercial entities. With the rise of direct-to-consumer genetic testing services, individuals' genetic data may be sold to third parties or used for purposes beyond the initial consent, leading to potential misuse of personal information. In countries with less stringent data protection laws, genetic information could be exploited for purposes such as genetic discrimination by insurers or employers.

There are also broader ethical considerations about the implications of genetic discoveries, particularly in relation to predictive testing for hereditary diseases. While early diagnosis can lead to better outcomes, it also raises questions about whether patients should know about conditions they may develop in the future, especially if no cure or treatment options are available. These concerns are compounded by varying legal frameworks across different countries regarding the use of genetic data. As the market expands, stakeholders must navigate these complex ethical issues to ensure public trust and compliance with data protection regulations.

Key Market Trends

Expansion of Clinical Applications

The expansion of clinical applications for whole genome sequencing (WGS) and whole exome sequencing (WES) is a key driver of their adoption across global healthcare systems. Once confined to research, these cutting-edge technologies now play pivotal roles in diagnosing complex genetic disorders, managing hereditary diseases, and optimizing cancer treatment strategies. Their versatility and precision have positioned them as indispensable tools in modern medicine, significantly contributing to market growth. In oncology, WGS and WES are transforming cancer care by enabling the precise identification of genetic mutations that drive tumor development. This level of specificity helps oncologists tailor targeted therapies, improving treatment outcomes and reducing unnecessary side effects. These technologies facilitate monitoring of treatment response by tracking tumor-specific genetic changes over time, ensuring adaptive and effective care strategies.

Rare disease diagnosis represents another critical area of application. Many rare genetic conditions remain undiagnosed due to their intricate nature and overlapping clinical symptoms. WGS and WES provide comprehensive genomic insights, dramatically improving diagnostic accuracy. By identifying causative genetic mutations, these technologies allow clinicians to implement earlier interventions and more personalized care, alleviating the diagnostic odyssey for patients and families.

Emerging applications further underscore the growing utility of WGS and WES. In reproductive medicine, they are increasingly used for preimplantation genetic testing to identify potential genetic risks in embryos during in vitro fertilization. In pharmacogenomics, they support personalized medicine by predicting patient responses to drugs based on genetic profiles, minimizing adverse reactions and optimizing treatment efficacy. Their role in infectious disease management is expanding, with applications such as tracking pathogen mutations and guiding outbreak containment strategies. As sequencing technologies advance, making them faster, more accurate, and cost-effective, the integration of WGS and WES into routine clinical practice is accelerating. Their broadening applications in diverse areas of healthcare continue to drive demand, cementing their role in shaping the future of personalized medicine and genomics-driven healthcare.

Rising Government and Private Investments in Genomics

Rising government and private investments in genomics are a major catalyst for the growth of the Global Whole Genome and Exome Sequencing (WGS and WES) Market. Governments across the globe are recognizing the transformative potential of genomic technologies in improving healthcare outcomes and addressing public health challenges. Initiatives such as the UK's 100,000 Genomes Project and the U.S.'s All of Us Research Program aim to build extensive genomic databases that serve as critical resources for advancing precision medicine. These programs not only drive research but also foster the integration of WGS and WES into routine clinical care, enabling personalized treatments and disease prevention strategies. Private sector contributions are equally significant in propelling the genomics landscape. Biotechnology companies, research institutions, and healthcare organizations are channeling substantial resources into genomic research and development. This funding supports the creation of cutting-edge sequencing technologies, sophisticated bioinformatics platforms, and scalable data storage solutions to manage and analyze the massive volumes of genomic data generated. These innovations are essential for enhancing the efficiency, accuracy, and accessibility of WGS and WES, thereby expanding their adoption across various sectors.

Venture capital firms are also playing a crucial role by investing heavily in genomics startups. These investments provide startups with the capital needed to develop disruptive technologies, explore novel applications, and penetrate emerging markets. Companies focusing on niche areas such as single-cell sequencing, long-read sequencing, and artificial intelligence-driven genomic analysis are particularly attractive to investors, fostering a dynamic and competitive market environment. The synergy between public and private funding is accelerating technological advancements and driving down the costs of sequencing, making WGS and WES more accessible. As these funding streams continue to grow, they are expected to not only expand the applications of genomic sequencing but also catalyze its adoption in healthcare systems worldwide. This investment trend underscores the increasing recognition of genomics as a cornerstone of modern medicine and innovation.

Segmental Insights

Product Insights

Based on the product, the instruments segment is currently dominating the Global Whole Genome and Exome Sequencing Market. This dominance is primarily driven by the increasing adoption of next-generation sequencing (NGS) platforms, which are essential for whole genome and exome sequencing. These instruments, such as high-throughput sequencers, are the backbone of genomic research and clinical applications, enabling large-scale sequencing projects with high accuracy and efficiency.

NGS instruments are equipped with advanced technologies that allow the sequencing of entire genomes or exomes in a relatively short time frame and at a lower cost compared to traditional methods. The development of high-throughput sequencers, such as Illumina's NovaSeq and Thermo Fisher's Ion Proton, has significantly boosted the ability to sequence large numbers of samples rapidly, making them integral to both clinical diagnostics and research endeavors. As the demand for precision medicine, cancer genomics, and genetic disease testing grows, the need for these sophisticated sequencing instruments continues to increase. The instruments segment benefits from ongoing technological advancements, such as the integration of artificial intelligence (AI) for data analysis, which enhances the capability of sequencing platforms. These innovations improve the accuracy, speed, and cost-effectiveness of sequencing, further solidifying the instruments segment's dominance in the market.

Application Insights

Based on the Application, Whole Genome Sequencing (WGS) is currently dominating the Global Whole Genome and Exome Sequencing Market. The widespread adoption of WGS can be attributed to its ability to provide a comprehensive analysis of the entire genome, including both coding and non-coding regions, making it highly valuable for a variety of applications. WGS allows researchers and clinicians to detect a broader range of genetic variations, such as single nucleotide polymorphisms (SNPs), insertions, deletions, and structural variants, which are crucial for understanding complex diseases like cancer, cardiovascular disorders, and neurological conditions.

In clinical diagnostics, WGS is increasingly being used for rare disease diagnosis, as it enables the identification of disease-causing mutations that may not be detected through other methods like whole exome sequencing (WES), which only focuses on the protein-coding regions of the genome. WGS has become an essential tool in precision medicine, as it provides a complete genetic profile of patients, facilitating personalized treatment plans based on genetic makeup. The technological advancements in sequencing platforms and the decreasing cost of WGS have made it more accessible for both research and clinical applications. This, combined with its ability to provide a more comprehensive understanding of the genome, is driving the market share of WGS over WES.

Regional Insights

North America is currently dominating the Global Whole Genome and Exome Sequencing Market, driven primarily by the United States, which leads in both technological advancements and healthcare infrastructure. The region benefits from a strong presence of major sequencing technology providers, including Illumina, Thermo Fisher Scientific, and Pacific Biosciences, which drive innovation and adoption of sequencing technologies. The U.S. has well-established regulatory frameworks and a robust healthcare system that supports the integration of whole genome and exome sequencing into clinical practice.

The demand for whole genome and exome sequencing in North America is fueled by its wide application in personalized medicine, oncology, rare disease diagnosis, and genetic research. The region is also home to numerous academic institutions and research organizations that are at the forefront of genomic studies, further propelling the market growth. Ongoing government initiatives, such as the U.S. Precision Medicine Initiative, provide funding and support for genomic research, encouraging broader use of sequencing technologies. North America's strong healthcare reimbursement system for genetic testing and the increasing focus on precision medicine and targeted therapies contribute to the dominance of this region.

Key Market Players

  • Agilent Technologies, Inc.
  • Thermo Fisher Scientific, Inc.
  • Bio-Rad Laboratories, Inc.
  • Eurofins Scientific SE
  • F. Hoffmann-La Roche Ltd
  • Illumina, Inc.
  • Laboratory Corporation of America Holdings
  • Novogene Corporation
  • Pacific Biosciences of California, Inc.
  • QIAGEN N.V.

Report Scope:

In this report, the Global Whole Genome and Exome Sequencing Market has been segmented into the following categories, in addition to the industry trends which have also been detailed below:

Whole Genome and Exome Sequencing Market, By Product:

  • Kits
  • Instruments

Whole Genome and Exome Sequencing Market, By Application:

  • Whole Genome Sequencing
  • Whole Exome Sequencing

Whole Genome and Exome Sequencing Market, By End-User:

  • Pharmaceutical and Biotechnology Companies
  • Diagnostic Laboratories
  • Hospitals and Clinics
  • Research and Academic Institutes
  • Others

Whole Genome and Exome Sequencing Market, By Region:

  • North America
    • United States
    • Canada
    • Mexico
  • Europe
    • France
    • United Kingdom
    • Italy
    • Germany
    • Spain
  • Asia-Pacific
    • China
    • India
    • Japan
    • Australia
    • South Korea
  • South America
    • Brazil
    • Argentina
    • Colombia
  • Middle East & Africa
    • South Africa
    • Saudi Arabia
    • UAE

Competitive Landscape

Company Profiles: Detailed analysis of the major companies present in the Global Whole Genome and Exome Sequencing Market.

Available Customizations:

Global Whole Genome and Exome Sequencing Market report with the given market data, TechSci Research offers customizations according to a company's specific needs. The following customization options are available for the report:

Company Information

  • Detailed analysis and profiling of additional market players (up to five).

Table of Contents

1. Product Overview

  • 1.1. Market Definition
  • 1.2. Scope of the Market
    • 1.2.1. Markets Covered
    • 1.2.2. Years Considered for Study
    • 1.2.3. Key Market Segmentations

2. Research Methodology

  • 2.1. Objective of the Study
  • 2.2. Baseline Methodology
  • 2.3. Key Industry Partners
  • 2.4. Major Association and Secondary Sources
  • 2.5. Forecasting Methodology
  • 2.6. Data Triangulation & Validation
  • 2.7. Assumptions and Limitations

3. Executive Summary

  • 3.1. Overview of the Market
  • 3.2. Overview of Key Market Segmentations
  • 3.3. Overview of Key Market Players
  • 3.4. Overview of Key Regions/Countries
  • 3.5. Overview of Market Drivers, Challenges, and Trends

4. Voice of Customer

5. Global Whole Genome and Exome Sequencing Market Outlook

  • 5.1. Market Size & Forecast
    • 5.1.1. By Value
  • 5.2. Market Share & Forecast
    • 5.2.1. By Product (Kits, Instruments)
    • 5.2.2. By Application (Whole Genome Sequencing (Oncology, Microbial, Non-Invasive Prenatal Testing (NIPT), Others), Whole Exome Sequencing (Oncology, Rare Disease, Gene Discovery, Others))
    • 5.2.3. By End-User (Pharmaceutical and Biotechnology Companies, Diagnostic Laboratories, Hospitals and Clinics, Research and Academic Institutes, Others)
    • 5.2.4. By Company (2023)
    • 5.2.5. By Region
  • 5.3. Market Map

6. North America Whole Genome and Exome Sequencing Market Outlook

  • 6.1. Market Size & Forecast
    • 6.1.1. By Value
  • 6.2. Market Share & Forecast
    • 6.2.1. By Product
    • 6.2.2. By Application
    • 6.2.3. By End-User
    • 6.2.4. By Country
  • 6.3. North America: Country Analysis
    • 6.3.1. United States Whole Genome and Exome Sequencing Market Outlook
      • 6.3.1.1. Market Size & Forecast
        • 6.3.1.1.1. By Value
      • 6.3.1.2. Market Share & Forecast
        • 6.3.1.2.1. By Product
        • 6.3.1.2.2. By Application
        • 6.3.1.2.3. By End-User
    • 6.3.2. Mexico Whole Genome and Exome Sequencing Market Outlook
      • 6.3.2.1. Market Size & Forecast
        • 6.3.2.1.1. By Value
      • 6.3.2.2. Market Share & Forecast
        • 6.3.2.2.1. By Product
        • 6.3.2.2.2. By Application
        • 6.3.2.2.3. By End-User
    • 6.3.3. Canada Whole Genome and Exome Sequencing Market Outlook
      • 6.3.3.1. Market Size & Forecast
        • 6.3.3.1.1. By Value
      • 6.3.3.2. Market Share & Forecast
        • 6.3.3.2.1. By Product
        • 6.3.3.2.2. By Application
        • 6.3.3.2.3. By End-User

7. Europe Whole Genome and Exome Sequencing Market Outlook

  • 7.1. Market Size & Forecast
    • 7.1.1. By Value
  • 7.2. Market Share & Forecast
    • 7.2.1. By Product
    • 7.2.2. By Application
    • 7.2.3. By End-User
    • 7.2.4. By Country
  • 7.3. Europe: Country Analysis
    • 7.3.1. France Whole Genome and Exome Sequencing Market Outlook
      • 7.3.1.1. Market Size & Forecast
        • 7.3.1.1.1. By Value
      • 7.3.1.2. Market Share & Forecast
        • 7.3.1.2.1. By Product
        • 7.3.1.2.2. By Application
        • 7.3.1.2.3. By End-User
    • 7.3.2. Germany Whole Genome and Exome Sequencing Market Outlook
      • 7.3.2.1. Market Size & Forecast
        • 7.3.2.1.1. By Value
      • 7.3.2.2. Market Share & Forecast
        • 7.3.2.2.1. By Product
        • 7.3.2.2.2. By Application
        • 7.3.2.2.3. By End-User
    • 7.3.3. United Kingdom Whole Genome and Exome Sequencing Market Outlook
      • 7.3.3.1. Market Size & Forecast
        • 7.3.3.1.1. By Value
      • 7.3.3.2. Market Share & Forecast
        • 7.3.3.2.1. By Product
        • 7.3.3.2.2. By Application
        • 7.3.3.2.3. By End-User
    • 7.3.4. Italy Whole Genome and Exome Sequencing Market Outlook
      • 7.3.4.1. Market Size & Forecast
        • 7.3.4.1.1. By Value
      • 7.3.4.2. Market Share & Forecast
        • 7.3.4.2.1. By Product
        • 7.3.4.2.2. By Application
        • 7.3.4.2.3. By End-User
    • 7.3.5. Spain Whole Genome and Exome Sequencing Market Outlook
      • 7.3.5.1. Market Size & Forecast
        • 7.3.5.1.1. By Value
      • 7.3.5.2. Market Share & Forecast
        • 7.3.5.2.1. By Product
        • 7.3.5.2.2. By Application
        • 7.3.5.2.3. By End-User

8. Asia-Pacific Whole Genome and Exome Sequencing Market Outlook

  • 8.1. Market Size & Forecast
    • 8.1.1. By Value
  • 8.2. Market Share & Forecast
    • 8.2.1. By Product
    • 8.2.2. By Application
    • 8.2.3. By End-User
    • 8.2.4. By Country
  • 8.3. Asia-Pacific: Country Analysis
    • 8.3.1. China Whole Genome and Exome Sequencing Market Outlook
      • 8.3.1.1. Market Size & Forecast
        • 8.3.1.1.1. By Value
      • 8.3.1.2. Market Share & Forecast
        • 8.3.1.2.1. By Product
        • 8.3.1.2.2. By Application
        • 8.3.1.2.3. By End-User
    • 8.3.2. India Whole Genome and Exome Sequencing Market Outlook
      • 8.3.2.1. Market Size & Forecast
        • 8.3.2.1.1. By Value
      • 8.3.2.2. Market Share & Forecast
        • 8.3.2.2.1. By Product
        • 8.3.2.2.2. By Application
        • 8.3.2.2.3. By End-User
    • 8.3.3. South Korea Whole Genome and Exome Sequencing Market Outlook
      • 8.3.3.1. Market Size & Forecast
        • 8.3.3.1.1. By Value
      • 8.3.3.2. Market Share & Forecast
        • 8.3.3.2.1. By Product
        • 8.3.3.2.2. By Application
        • 8.3.3.2.3. By End-User
    • 8.3.4. Japan Whole Genome and Exome Sequencing Market Outlook
      • 8.3.4.1. Market Size & Forecast
        • 8.3.4.1.1. By Value
      • 8.3.4.2. Market Share & Forecast
        • 8.3.4.2.1. By Product
        • 8.3.4.2.2. By Application
        • 8.3.4.2.3. By End-User
    • 8.3.5. Australia Whole Genome and Exome Sequencing Market Outlook
      • 8.3.5.1. Market Size & Forecast
        • 8.3.5.1.1. By Value
      • 8.3.5.2. Market Share & Forecast
        • 8.3.5.2.1. By Product
        • 8.3.5.2.2. By Application
        • 8.3.5.2.3. By End-User

9. South America Whole Genome and Exome Sequencing Market Outlook

  • 9.1. Market Size & Forecast
    • 9.1.1. By Value
  • 9.2. Market Share & Forecast
    • 9.2.1. By Product
    • 9.2.2. By Application
    • 9.2.3. By End-User
    • 9.2.4. By Country
  • 9.3. South America: Country Analysis
    • 9.3.1. Brazil Whole Genome and Exome Sequencing Market Outlook
      • 9.3.1.1. Market Size & Forecast
        • 9.3.1.1.1. By Value
      • 9.3.1.2. Market Share & Forecast
        • 9.3.1.2.1. By Product
        • 9.3.1.2.2. By Application
        • 9.3.1.2.3. By End-User
    • 9.3.2. Argentina Whole Genome and Exome Sequencing Market Outlook
      • 9.3.2.1. Market Size & Forecast
        • 9.3.2.1.1. By Value
      • 9.3.2.2. Market Share & Forecast
        • 9.3.2.2.1. By Product
        • 9.3.2.2.2. By Application
        • 9.3.2.2.3. By End-User
    • 9.3.3. Colombia Whole Genome and Exome Sequencing Market Outlook
      • 9.3.3.1. Market Size & Forecast
        • 9.3.3.1.1. By Value
      • 9.3.3.2. Market Share & Forecast
        • 9.3.3.2.1. By Product
        • 9.3.3.2.2. By Application
        • 9.3.3.2.3. By End-User

10. Middle East and Africa Whole Genome and Exome Sequencing Market Outlook

  • 10.1. Market Size & Forecast
    • 10.1.1. By Value
  • 10.2. Market Share & Forecast
    • 10.2.1. By Product
    • 10.2.2. By Application
    • 10.2.3. By End-User
    • 10.2.4. By Country
  • 10.3. MEA: Country Analysis
    • 10.3.1. South Africa Whole Genome and Exome Sequencing Market Outlook
      • 10.3.1.1. Market Size & Forecast
        • 10.3.1.1.1. By Value
      • 10.3.1.2. Market Share & Forecast
        • 10.3.1.2.1. By Product
        • 10.3.1.2.2. By Application
        • 10.3.1.2.3. By End-User
    • 10.3.2. Saudi Arabia Whole Genome and Exome Sequencing Market Outlook
      • 10.3.2.1. Market Size & Forecast
        • 10.3.2.1.1. By Value
      • 10.3.2.2. Market Share & Forecast
        • 10.3.2.2.1. By Product
        • 10.3.2.2.2. By Application
        • 10.3.2.2.3. By End-User
    • 10.3.3. UAE Whole Genome and Exome Sequencing Market Outlook
      • 10.3.3.1. Market Size & Forecast
        • 10.3.3.1.1. By Value
      • 10.3.3.2. Market Share & Forecast
        • 10.3.3.2.1. By Product
        • 10.3.3.2.2. By Application
        • 10.3.3.2.3. By End-User

11. Market Dynamics

  • 11.1. Drivers
  • 11.2. Challenges

12. Market Trends & Developments

  • 12.1. Merger & Acquisition (If Any)
  • 12.2. Product Launches (If Any)
  • 12.3. Recent Developments

13. Porters Five Forces Analysis

  • 13.1. Competition in the Industry
  • 13.2. Potential of New Entrants
  • 13.3. Power of Suppliers
  • 13.4. Power of Customers
  • 13.5. Threat of Substitute Products

14. Competitive Landscape

  • 14.1. Agilent Technologies, Inc.
    • 14.1.1. Business Overview
    • 14.1.2. Company Snapshot
    • 14.1.3. Products & Services
    • 14.1.4. Financials (As Reported)
    • 14.1.5. Recent Developments
    • 14.1.6. Key Personnel Details
    • 14.1.7. SWOT Analysis
  • 14.2. Thermo Fisher Scientific, Inc.
  • 14.3. Bio-Rad Laboratories, Inc.
  • 14.4. Eurofins Scientific SE
  • 14.5. F. Hoffmann-La Roche Ltd
  • 14.6. Illumina, Inc.
  • 14.7. Laboratory Corporation of America Holdings
  • 14.8. Novogene Corporation
  • 14.9. Pacific Biosciences of California, Inc.
  • 14.10. QIAGEN N.V.

15. Strategic Recommendations

16. About Us & Disclaimer