시장보고서
상품코드
1722975

세계의 유전자 검사 시장 규모, 점유율, 동향, 예측 : 유형, 기술, 용도, 지역별(2025-2033년)

Genetic Testing Market Size, Share, Trends and Forecast by Type, Technology, Application, and Region, 2025-2033

발행일: | 리서치사: IMARC | 페이지 정보: 영문 144 Pages | 배송안내 : 2-3일 (영업일 기준)

    
    
    




※ 본 상품은 영문 자료로 한글과 영문 목차에 불일치하는 내용이 있을 경우 영문을 우선합니다. 정확한 검토를 위해 영문 목차를 참고해주시기 바랍니다.

유전자 검사 세계 시장 규모는 2024년 195억 달러에 달했습니다. 향후 IMARC Group은 2033년에는 448억 8,000만 달러에 이르고, 2025-2033년 9.70%의 연평균 복합 성장률(CAGR)을 보일 것으로 예측했습니다. 현재 북미가 시장을 독점하고 있으며, 2024년 시장 점유율은 45.6% 이상에 달했습니다. 북미 시장의 주요 원동력은 기술 발전, 개인 맞춤형 의료에 대한 수요 증가, 유전성 질환의 유병률 증가, 정부의 지원책 도입, 윤리적, 법적, 사회적 배려의 의미 증가 등입니다.

유전자 검사 시장 분석 :

시장 성장과 규모: 이 분야는 일반 대중이 더 많은 정보를 얻고 개인 맞춤형 의료에 대한 욕구가 증가함에 따라 강력한 성장세를 보이고 있습니다. 검사 기술의 발전과 함께 시장은 매우 빠른 속도로 새로운 헬스케어 분야에 침투하고 있으며, 헬스케어 업계에서 가장 역동적인 분야 중 하나가 되고 있습니다.

주요 시장 성장 촉진요인 : 주요 요인은 신기술의 도입, 유전성 질환 및 만성 질환의 유병률 증가, 유전적 위험에 대한 소비자 지식 증가입니다. 또한, 정부의 이니셔티브와 유전자 조사에 대한 자금 지원도 시장 성장을 크게 촉진하고 있으며, 유전자 검사 시장이 어느 정도 규모인지에 대한 정확한 해답이 되고 있습니다.

기술 발전: NGS(차세대 염기서열 분석)와 CRISPR 기술의 혁신은 정확하고 합리적인 비용으로 검사에 혁명을 일으켰습니다. 이러한 발전은 유전자 검사의 범위와 기회를 확대했으며, 그 결과 임상 현장과 연구 개발 모두에서 유전자 검사의 사용량이 증가하고 있습니다.

산업용도: 검사 용도에는 암 진단, 유전자 질환 진단, 심혈관 질환 진단 등이 포함됩니다. 유전성 질환의 진단 및 관리에도 사용할 수 있기 때문에 현대 헬스케어와 떼려야 뗄 수 없는 존재가 되었습니다.

주요 시장 동향 : 의사의 개입 없이 유전자 정보를 얻을 수 있는 소비자 직접 서비스에 대한 선호도가 높아지고 있습니다. 또한, 질병 검진 및 관리를 위해 검사가 일상적인 건강관리의 일부로 자리잡아가고 있는 추세도 유전자 검사 시장 전망을 밝게 하고 있습니다.

지리적 동향 : 북미가 시장을 주도하고 유럽, 아시아태평양이 그 뒤를 잇고 있습니다. 의료 시설, 1인당 의료비, 정부 지원 등의 요인도 이들 지역의 발전에 기여하고 있습니다. 라틴아메리카와 중동 및 아프리카의 신흥 시장은 현재의 어려움에도 불구하고 성장 잠재력을 보여주고 있습니다.

경쟁 구도: 시장 경쟁이 치열하고, 주요 기업들은 연구개발, 전략적 제휴, 규제 준수에 힘쓰고 있습니다. 이들 기업은 경쟁력을 유지하기 위해 검사 포트폴리오를 확장하고 새로운 시장 기회를 개척하는 데 주력하고 있습니다.

과제와 기회: 시장은 큰 성장 기회를 제공하는 반면, 검사의 윤리적, 법적 의미, 숙련된 전문가의 필요성, 사회적 인식 문제 등의 문제에 직면해 있습니다. 이러한 과제를 해결하고 기술 발전을 활용하면 시장 확대와 혁신의 큰 기회를 얻을 수 있습니다.

유전자 검사 시장 동향 :

유전자 검사 기술의 발전

유전자 검사 시장 규모를 견인하고 있는 것은 유전자 검사 기술의 발전입니다. 이러한 기술 혁신으로 보다 정확하고 효율적이며 비용 효율적인 유전자 분석법이 개발되어 종양학, 약리유전체학, 예측 검사 등의 분야로 검사 범위가 확대되면서 유전자 검사 시장의 성장을 더욱 촉진하고 있습니다. 차세대 염기서열 분석(NGS)과 같은 향상된 염기서열 분석 기술은 유전자 질환에 대한 심층적인 통찰력을 제공하여 조기 발견과 맞춤형 치료 계획을 가능하게 합니다. 예를 들어

1,914명의 여성을 대상으로 한 연구에서 cfDNA 검사는 표준 검사에 비해 21번 삼염색체와 18번 삼염색체의 위양성을 크게 감소시켰으며, 이형접합성 검출 성공률은 100%로 높은 예측력을 보였습니다. 또한, 간소화된 프로세스로 인해 다양한 의료 현장에서 유전자 검사의 채택이 증가하여 유전자 검사 시장 수요에 기여하고 있습니다.

개인 맞춤형 의료에 대한 인식과 수요 증가

개인 맞춤형 의료에 대한 인식과 수요 증가도 유전자 검사 시장 전망을 형성하는 데 중요한 역할을 하고 있습니다. 맞춤의료는 유전자 정보에 의존하여 치료를 맞춤화하는 것으로, 유전자 검사에 대한 수요를 높이고 있습니다. 이러한 수요는 유전자 검사가 치료 방침을 결정하고 자손의 유전적 질병 위험을 평가하는 종양학이나 생식 의학 등의 분야에서 특히 두드러집니다. 예를 들어, 응답률 36%의 조사에 따르면, 312명의 응답자 중 83%가 유전자 검사에 대한 문의를 최소화하고, 14%가 결과 해석에 대응하며, 50% 이상이 유전자 검사의 유전상담사 및 임상 현장에서의 역할을 지지하고, 70%가 프라이버시, 익명성, 접근성에 대한 우려를 가지고 있는 것으로 나타났습니다. 환자에게 유전자 검사를 고려하는 것에 대해 긍정적이었습니다. 또한, 건강 상태에 대한 유전적 소인을 이해하는 것에 대한 소비자의 관심이 높아지면서 유전자 검사 시장 전망을 더욱 촉진하고, 유전자 검사 시장 통계와 유전자 검사 시장 동향을 주도하고 있습니다.

유전성 질환과 만성질환 증가

세계적으로 유전성 질환과 만성 질환 증가는 유전자 검사 시장 통계를 더욱 확대시키고 있습니다. 유전자 검사는 낭포성 섬유증, 겸상 적혈구 빈혈, 헌팅턴병 등 다양한 질환의 조기 발견, 진단 및 관리에 중요한 역할을 하고 있습니다. 또한, 암, 심혈관계 질환, 당뇨병과 같은 만성질환의 발생률이 증가함에 따라 이들 질환의 소인이 되는 유전자 변이를 확인하기 위한 검사의 필요성이 증가하고 있습니다. 세계보건기구(WHO)의 보고에 따르면 암, 심혈관질환, 당뇨병과 같은 비감염성 질환(NCDs)은 전 세계 연간 사망자 수의 73%를 차지합니다. 유전자 검사는 이러한 질병에 걸릴 위험이 있는 사람을 식별하는 데 도움이 됩니다. 검사를 통한 조기 발견은 환자의 예후를 개선하고 유전자 검사 시장을 더욱 촉진합니다. 유전자 검사 시장은 크고, 미국 및 기타 신흥국에서는 연간 유전자 검사 건수가 크게 증가하고 있습니다. 유전자 검사의 미래가 밝고, 기술의 발전으로 정확성과 접근성이 향상될 것으로 예측됩니다. 임신 중 유전자 검사도 점점 더 널리 보급되어 태아의 건강 상태와 유전적 상태에 대한 귀중한 통찰력을 제공합니다.

목차

제1장 서문

제2장 조사 범위와 조사 방법

  • 조사 목적
  • 이해관계자
  • 데이터 소스
    • 1차 정보
    • 2차 정보
  • 시장 추정
    • 보텀업 접근
    • 톱다운 접근
  • 조사 방법

제3장 주요 요약

제4장 서론

  • 개요
  • 주요 업계 동향

제5장 세계의 유전자 검사 시장

  • 시장 개요
  • 시장 실적
  • COVID-19의 영향
  • 시장 예측

제6장 시장 분석 : 유형별

  • 예측 및 발증전 검사
  • 캐리어 테스트
  • 산전 검사 및 신생아 검사
  • 진단 검사
  • 약물유전체학 검사
  • 기타

제7장 시장 분석 : 기술별

  • 세포 유전학적 검사 및 염색체 분석
  • 생화학 검사
  • 분자 검사
    • 주요 부문
      • DNA 시퀀싱
      • 기타

제8장 시장 분석 : 용도별

  • 암 진단
  • 유전성 질환 진단
  • 심혈관 질환 진단
  • 기타

제9장 시장 분석 : 지역별

  • 북미
    • 미국
    • 캐나다
  • 아시아태평양
    • 중국
    • 일본
    • 인도
    • 한국
    • 호주
    • 인도네시아
    • 기타
  • 유럽
    • 독일
    • 프랑스
    • 영국
    • 이탈리아
    • 스페인
    • 러시아
    • 기타
  • 라틴아메리카
    • 브라질
    • 멕시코
    • 기타
  • 중동 및 아프리카
    • 시장 내역 : 국가별

제10장 SWOT 분석

  • 개요
  • 강점
  • 약점
  • 기회
  • 위협

제11장 밸류체인 분석

제12장 Porter의 Five Forces 분석

  • 개요
  • 바이어의 교섭력
  • 공급 기업의 교섭력
  • 경쟁 정도
  • 신규 진출업체의 위협
  • 대체품의 위협

제13장 가격 분석

제14장 경쟁 구도

  • 시장 구조
  • 주요 기업
  • 주요 기업 개요
    • 23andme Inc.
    • Ambry Genetics Corporation(Konica Minolta Healthcare Americas Inc.)
    • Bio-RAD Laboratories Inc.
    • Cepheid(Danaher Corporation)
    • Eurofins Scientific
    • Illumina Inc.
    • Invitae Corporation
    • Luminex Corporation(DiaSorin)
    • Myriad Genetics Inc.
    • QIAGEN
    • Quest Diagnostics
    • Thermo Fisher Scientific
LSH 25.06.05

The global genetic testing market size was valued at USD 19.5 Billion in 2024. Looking forward, IMARC Group estimates the market to reach USD 44.88 Billion by 2033, exhibiting a CAGR of 9.70% from 2025-2033. North America currently dominates the market, holding a market share of over 45.6% in 2024. The North American market is primarily driven by technological advancements, escalating demand for personalized medicine, rising prevalence of genetic disorders, introduction of supportive government initiatives, and increasing implication of ethical, legal, and social considerations.

Genetic Testing Market Analysis:

Market Growth and Size: The sector is seeing strong growth as the public becomes more informed and the appetite for personalized medicine increases. With advancements in testing technologies, the market is penetrating new healthcare sectors at an extremely rapid pace and has become one of the most dynamic segments of the healthcare industry.

Major Market Drivers: The main factors are the introduction of new technologies, the increase in the prevalence of genetic diseases and chronic conditions and the increasing of the consumer's knowledge about genetic risks. Government initiatives and funding of genetic research also greatly assist the industry in market growth, which provide an accurate answer to how big is the genetic testing market.

Technological Advancements: Innovations in NGS (next-generation sequencing) and CRISPR technologies have revolutionized testing providing precise and budget-friendly methods. These developments have enlarged the range and opportunity of genetic testing, which in turn has increased the usage of it both in clinical settings and in research.

Industry Applications: The application of the testing includes cancer diagnosis, genetic disease diagnosis, and cardiovascular disease diagnosis. It can be used for diagnosing and managing genetic diseases makes it an inseparable part of modern healthcare.

Key Market Trends: There is a rising preference for direct-to-consumer services, in which users can acquire genetic information without using an intervening doctor. The market is also experiencing a trend where testing is becoming part of regular healthcare practices for disease screening and management, which indicates a positive outlook for the future of genetic testing market.

Geographical Trends: North America dominates the market, followed by Europe and the Asia Pacific. Factors including healthcare facilities, per capita medical expenditure, and governmental assistance also contribute to the development of these regions. Emerging markets in Latin America and the Middle East and Africa show potential for growth despite current challenges.

Competitive Landscape: The market is highly competitive with key players engaging in research and development, strategic partnerships, and regulatory compliance. These companies are focusing on expanding their testing portfolios and exploring new market opportunities to maintain their competitive edge.

Challenges and Opportunities: While the market offers substantial growth opportunities, it faces challenges such as ethical and legal implications of testing, the need for skilled professionals, and public perception issues. Addressing these challenges and harnessing technological advancements present significant opportunities for market expansion and innovation.

Genetic Testing Market Trends:

Advancements in genetic testing technologies

Advancements in genetic testing technologies have been instrumental in driving the genetic testing market size. These technological innovations have led to more accurate, efficient, and cost-effective genetic analysis methods, expanding the scope of testing into areas such as oncology, pharmacogenomics, and predictive testing, further driving the genetic testing market growth. Enhanced sequencing techniques, such as next-generation sequencing (NGS), provide detailed insights into genetic disorders, enabling early detection and personalized treatment plans. For instance,

A study on 1914 women revealed cfDNA testing significantly reduces false positives for trisomies 21 and 18 compared to standard screening, with a 100% success rate in detecting aneuploidies and higher predictive values. Furthermore, simplified processes have increased the adoption of genetic testing across various healthcare settings, contributing to the genetic testing market demand.

Increasing awareness and demand for personalized medicine

Increasing awareness and demand for personalized medicine have also played a significant role in shaping the genetic testing market outlook. Personalized medicine, which relies on genetic information to tailor treatments, has heightened the demand for genetic tests. This demand is particularly evident in sectors such as oncology and reproductive health, where genetic testing guides therapy decisions and assesses genetic disorder risks in offspring. For example, according to a study, survey with a 36% response rate showed that 83% of the 312 respondents had minimal inquiries about direct-to-consumer genetic testing, 14% dealt with result interpretation, and over 50% supported the role of genetic counsellors and clinical settings for genetic testing, with 70% open to considering it for patients with privacy, anonymity, or access concerns. Additionally, growing consumer interest in understanding genetic predispositions to health conditions further fuels genetic testing market overview, driving genetic testing market statistics and genetic testing market trends.

Rise in genetic disorders and chronic diseases

The rise in genetic disorders and chronic diseases globally is further escalating the genetic testing market statistics. Genetic testing plays a vital role in the early detection, diagnosis, and management of various conditions such as cystic fibrosis, sickle cell anemia, and Huntington's disease. Moreover, with the increasing incidence of chronic diseases, including cancer, cardiovascular diseases, and diabetes, there is a heightened need for testing to identify genetic mutations predisposing individuals to these conditions. The World Health Organization (WHO) reports that non-communicable diseases (NCDs), such as cancer, cardiovascular diseases, and diabetes, are responsible for 73% of global deaths annually. Genetic testing can help identify individuals at risk for these conditions. Early detection through testing improves patient outcomes, further propels the genetic testing market. The genetic testing market is substantial, with a considerable growth in the number of genetic testing per year in USA and other developed countries. Looking ahead, the future of genetic testing is promising, with continued technological advancements expected to enhance accuracy and accessibility. Genetic testing in pregnancy is also becoming increasingly prevalent, providing valuable insights into fetal health and genetic conditions.

Genetic Testing Industry Segmentation:

Breakup by Type:

  • Predictive and Presymptomatic Testing
  • Carrier Testing
  • Prenatal and Newborn Testing
  • Diagnostic Testing
  • Pharmacogenomic Testing
  • Others

Diagnostic testing accounts for the majority of the market share

The largest sector of the market is the diagnostic testing market, which is employed to reveal or confirm specific inherited disease in symptomatic people. This sector is on the rise due to its contribution to a precise diagnosis, which is necessary for appropriate treatment and control of a plethora of genetic conditions. The fact of its broad fields of using from rare genetical diseases till common conditions brings attention to this issue in medical sector. An investigation that appeared in the Journal of Molecular Diagnostics revealed that the percentage of medical professionals who had integrated genetic diagnostic testing for hereditary cancers definitely had grown from 19.8% in 2014 to 38.4% in 2018.

Breakup by Technology:

  • Cytogenetic Testing and Chromosome Analysis
  • Biochemical Testing
  • Molecular Testing
  • DNA Sequencing
  • Others

Molecular testing holds the largest share in the industry

Molecular testing represents the largest section in the market. The methodology portion cover PCR, NGS, and other filtered DNA related analysis terms. It is very practical as it can be applied for many sections, from detecting genetic changes that give rise to diseases, to exploring cancer genetics for the reason of targeted treatments, and to unearthing genetic predispositions for different conditions. The unique capability of molecular testing associated with the precision it offers has established the field of genetic diagnostics, individualized medicine, and research as a key area in molecular science, giving it a leading position in this field. A 2021 study evaluated various COVID-19 molecular tests, revealing a high sensitivity rate of 95.9% for minimizing false negatives, and a specificity rate of 97.2% to reduce false positives. Besides, cytogenetic testing, including chromosome analysis means looking through section of chromosome in attempted to get information about chromosomal abnormalities of the patient. This part has a vital role in recognition the chromosome count, missing only one chromosome could cause genetic disorders such as Down syndrome, Klinefelter syndrome or Turner syndrome. It is widely use in pre-natal testing, cancer diagnosis and also for studying cells chromosome change, which are hardly beyond disease.

The biochemical testing, on the other hand, is directed towards the measurement of the exact amount of activity in most cases of specific enzymes in the body or the levels of proteins, hormones and other substances that comprise the body. This segment is a vital step in identifying metabolic disorders that result from enzyme deficiency by determining conditions like PKU or Tay- Sachs Disease, as possible causes.

Breakup by Application:

  • Cancer Diagnosis
  • Genetic Disease Diagnosis
  • Cardiovascular Disease Diagnosis
  • Others

Genetic disease diagnosis represents the leading market segment

Genetic testing is currently utilized to diagnose a large number of diseases that are affected by both single-gene and multiple-gene factors. Genetic disease diagnosis is essential for the early detection of diseases and prompt intervention that finally aid in the condition's management. This growth is powered by its rear-rooted importance in the field of medicine which is represented in the accurate diagnoses of the genetic diseases not only for treatment but also for family planning. Between 2012 and 2022, the US led in the expansion of genetic tests, primarily for clinical diagnosis, highlighting the need for mandatory reporting and international collaboration for a comprehensive understanding of global genetic testing.

Using genetic analysis for cancer diagnosis implies finding out genetic mutations or alterations which cause cancer to develop. This portion is very vital for early tumor detection, diagnosis and controlling different categories of cancer.

Moreover, the genetic diagnosis of cardiovascular diseases involves locating these genetic variants to establish an increased risk for such heart-related defects as congenital heart defects, various cardiomyopathies, and arrhythmias.

Breakup by Region:

  • North America
  • United States
  • Canada
  • Asia-Pacific
  • China
  • Japan
  • India
  • South Korea
  • Australia
  • Indonesia
  • Others
  • Europe
  • Germany
  • France
  • United Kingdom
  • Italy
  • Spain
  • Russia
  • Others
  • Latin America
  • Brazil
  • Mexico
  • Others
  • Middle East and Africa

North America leads the market, accounting for the largest genetic testing market share

The market research report has also provided a comprehensive analysis of all the major regional markets, which include North America (the United States and Canada); Europe (Germany, France, the United Kingdom, Italy, Spain, Russia, and others); Asia Pacific (China, Japan, India, South Korea, Australia, Indonesia, and others); Latin America (Brazil, Mexico, and others); and the Middle East and Africa. According to the report, North America accounted for the largest market share.

North America is the largest segment in the world market, driven by the world class healthcare infrastructure, the high amount of money that is spent on the healthcare sector and the presence of top companies and research institutions. The region is propelled by strong private investment, in the field of personalized medicine, large investments by governments in gene research, and favorable policy decisions from the national government. Besides, genetic disorders as well as chronic diseases, with a growing number of patients and informed population ready to access testing services, boost propel this company's leading position in the market.

The European region remains of crucial importance in terms of the market structure which is based on well-developed healthcare systems and governmental financial support of genetic research. The locale's market growth is propelled by the growing awareness about genetic DNA, personalized medicine, and the availability of qualified personnel in the field of genetics.

The Asia Pacific region is experiencing a growing market come from the fact that it is a large population base, infrastructure on healthcare rising and increasing the expenditure on healthcare. The market also draws support from genetic disease awareness growth, personalized medicine demanded growth, and government initiatives in health care reform.

The Latin American market is developing steadily, it is stimulated by improvement of the healthcare infrastructure, by the growth of the wages, and by the increase in public health awareness. As region is faced with the increasing demand for testing services for diseases prevention, diagnosis, and treatment.

The middle east and Africa market holds a lot of promise of significant growth. Factors that include the rising number of healthcare expenditure, the growing prevalence of genetic diseases, as well as the heightened level of awareness of the significant effects of genetic testing across the industry are the major drivers of genetic testing in this part of the world.

Leading Key Players in the Genetic Testing Industry:

Market's key players adopt different strategies to achieve fundamental objective of strengthening their market share. This include is investing heavily in research and development to innovation and evolution of genetic testing technologies, especially in the direction of next-generation sequencing (NGS) and CRISPR. They also engage in the establishment of partnerships and collaboration with other biotech companies, academic institutions, as well as healthcare providers to help them grow in their services portfolio and geographical reach. Besides this, manufacturers are making efforts to get the new devices approved by the regulator agencies to be in compliance with regulations and guarantee the patient safety. Additionally, direct-to-consumer services have been developed with the aim of leveraging consumers' growing demand for personalized healthcare and genetic wellness.

The market research report has provided a comprehensive analysis of the competitive landscape. Detailed profiles of all major companies have also been provided. Some of the key players in the market include:

  • 23andme Inc.
  • Ambry Genetics Corporation (Konica Minolta Healthcare Americas Inc.)
  • Bio-RAD Laboratories Inc.
  • Cepheid (Danaher Corporation)
  • Eurofins Scientific
  • Illumina Inc.
  • Invitae Corporation
  • Luminex Corporation (DiaSorin)
  • Myriad Genetics Inc.
  • QIAGEN
  • Quest Diagnostics
  • Thermo Fisher Scientific

(Please note that this is only a partial list of the key players, and the complete list is provided in the report.)

Latest News:

11 July 2023: Quest Diagnostics launched Consumer-Initiated Genetic Test on questhealth.com to Deliver Personalized, Actionable Health Risk Insights. The new offering helps people understand their potential risk of developing certain inheritable health conditions, with advanced technology and end-to-end support that includes personalized health reports and access to genetic counseling.

14 April 2023: QIAGEN launched the Applied Biosystems QuantStudio Absolute Q Digital PCR System, the first fully integrated digital PCR (dPCR) system designed to provide highly accurate and consistent results within 90 minutes.

10 March 2022: Thermo Fisher Scientific introduced latest generation of SeqStudio Flex Series Genetic Analyzer to enable customer's cutting-edge research in areas such as gene editing and infectious disease.

Key Questions Answered in This Report

  • 1.What is genetic testing?
  • 2.How big is the genetic testing market?
  • 3.What is the expected growth rate of the global genetic testing market during 2025-2033?
  • 4.What are the key factors driving the global genetic testing market?
  • 5.What is the leading segment of the global genetic testing market based on type?
  • 6.What is the leading segment of the global genetic testing market based on technology?
  • 7.What is the leading segment of the global genetic testing market based on application?
  • 8.What are the key regions in the global genetic testing market?
  • 9.Who are the key players/companies in the global genetic testing market?

Table of Contents

1 Preface

2 Scope and Methodology

  • 2.1 Objectives of the Study
  • 2.2 Stakeholders
  • 2.3 Data Sources
    • 2.3.1 Primary Sources
    • 2.3.2 Secondary Sources
  • 2.4 Market Estimation
    • 2.4.1 Bottom-Up Approach
    • 2.4.2 Top-Down Approach
  • 2.5 Forecasting Methodology

3 Executive Summary

4 Introduction

  • 4.1 Overview
  • 4.2 Key Industry Trends

5 Global Genetic Testing Market

  • 5.1 Market Overview
  • 5.2 Market Performance
  • 5.3 Impact of COVID-19
  • 5.4 Market Forecast

6 Market Breakup by Type

  • 6.1 Predictive and Presymptomatic Testing
    • 6.1.1 Market Trends
    • 6.1.2 Market Forecast
  • 6.2 Carrier Testing
    • 6.2.1 Market Trends
    • 6.2.2 Market Forecast
  • 6.3 Prenatal and Newborn Testing
    • 6.3.1 Market Trends
    • 6.3.2 Market Forecast
  • 6.4 Diagnostic Testing
    • 6.4.1 Market Trends
    • 6.4.2 Market Forecast
  • 6.5 Pharmacogenomic Testing
    • 6.5.1 Market Trends
    • 6.5.2 Market Forecast
  • 6.6 Others
    • 6.6.1 Market Trends
    • 6.6.2 Market Forecast

7 Market Breakup by Technology

  • 7.1 Cytogenetic Testing and Chromosome Analysis
    • 7.1.1 Market Trends
    • 7.1.2 Market Forecast
  • 7.2 Biochemical Testing
    • 7.2.1 Market Trends
    • 7.2.2 Market Forecast
  • 7.3 Molecular Testing
    • 7.3.1 Market Trends
    • 7.3.2 Key Segments
      • 7.3.2.1 DNA Sequencing
      • 7.3.2.1 Others
    • 7.3.3 Market Forecast

8 Market Breakup by Application

  • 8.1 Cancer Diagnosis
    • 8.1.1 Market Trends
    • 8.1.2 Market Forecast
  • 8.2 Genetic Disease Diagnosis
    • 8.2.1 Market Trends
    • 8.2.2 Market Forecast
  • 8.3 Cardiovascular Disease Diagnosis
    • 8.3.1 Market Trends
    • 8.3.2 Market Forecast
  • 8.4 Others
    • 8.4.1 Market Trends
    • 8.4.2 Market Forecast

9 Market Breakup by Region

  • 9.1 North America
    • 9.1.1 United States
      • 9.1.1.1 Market Trends
      • 9.1.1.2 Market Forecast
    • 9.1.2 Canada
      • 9.1.2.1 Market Trends
      • 9.1.2.2 Market Forecast
  • 9.2 Asia-Pacific
    • 9.2.1 China
      • 9.2.1.1 Market Trends
      • 9.2.1.2 Market Forecast
    • 9.2.2 Japan
      • 9.2.2.1 Market Trends
      • 9.2.2.2 Market Forecast
    • 9.2.3 India
      • 9.2.3.1 Market Trends
      • 9.2.3.2 Market Forecast
    • 9.2.4 South Korea
      • 9.2.4.1 Market Trends
      • 9.2.4.2 Market Forecast
    • 9.2.5 Australia
      • 9.2.5.1 Market Trends
      • 9.2.5.2 Market Forecast
    • 9.2.6 Indonesia
      • 9.2.6.1 Market Trends
      • 9.2.6.2 Market Forecast
    • 9.2.7 Others
      • 9.2.7.1 Market Trends
      • 9.2.7.2 Market Forecast
  • 9.3 Europe
    • 9.3.1 Germany
      • 9.3.1.1 Market Trends
      • 9.3.1.2 Market Forecast
    • 9.3.2 France
      • 9.3.2.1 Market Trends
      • 9.3.2.2 Market Forecast
    • 9.3.3 United Kingdom
      • 9.3.3.1 Market Trends
      • 9.3.3.2 Market Forecast
    • 9.3.4 Italy
      • 9.3.4.1 Market Trends
      • 9.3.4.2 Market Forecast
    • 9.3.5 Spain
      • 9.3.5.1 Market Trends
      • 9.3.5.2 Market Forecast
    • 9.3.6 Russia
      • 9.3.6.1 Market Trends
      • 9.3.6.2 Market Forecast
    • 9.3.7 Others
      • 9.3.7.1 Market Trends
      • 9.3.7.2 Market Forecast
  • 9.4 Latin America
    • 9.4.1 Brazil
      • 9.4.1.1 Market Trends
      • 9.4.1.2 Market Forecast
    • 9.4.2 Mexico
      • 9.4.2.1 Market Trends
      • 9.4.2.2 Market Forecast
    • 9.4.3 Others
      • 9.4.3.1 Market Trends
      • 9.4.3.2 Market Forecast
  • 9.5 Middle East and Africa
    • 9.5.1 Market Trends
    • 9.5.2 Market Breakup by Country
    • 9.5.3 Market Forecast

10 SWOT Analysis

  • 10.1 Overview
  • 10.2 Strengths
  • 10.3 Weaknesses
  • 10.4 Opportunities
  • 10.5 Threats

11 Value Chain Analysis

12 Porters Five Forces Analysis

  • 12.1 Overview
  • 12.2 Bargaining Power of Buyers
  • 12.3 Bargaining Power of Suppliers
  • 12.4 Degree of Competition
  • 12.5 Threat of New Entrants
  • 12.6 Threat of Substitutes

13 Price Analysis

14 Competitive Landscape

  • 14.1 Market Structure
  • 14.2 Key Players
  • 14.3 Profiles of Key Players
    • 14.3.1 23andme Inc.
      • 14.3.1.1 Company Overview
      • 14.3.1.2 Product Portfolio
    • 14.3.2 Ambry Genetics Corporation (Konica Minolta Healthcare Americas Inc.)
      • 14.3.2.1 Company Overview
      • 14.3.2.2 Product Portfolio
    • 14.3.3 Bio-RAD Laboratories Inc.
      • 14.3.3.1 Company Overview
      • 14.3.3.2 Product Portfolio
      • 14.3.3.3 Financials
      • 14.3.3.4 SWOT Analysis
    • 14.3.4 Cepheid (Danaher Corporation)
      • 14.3.4.1 Company Overview
      • 14.3.4.2 Product Portfolio
      • 14.3.4.3 SWOT Analysis
    • 14.3.5 Eurofins Scientific
      • 14.3.5.1 Company Overview
      • 14.3.5.2 Product Portfolio
      • 14.3.5.3 Financials
      • 14.3.5.4 SWOT Analysis
    • 14.3.6 Illumina Inc.
      • 14.3.6.1 Company Overview
      • 14.3.6.2 Product Portfolio
      • 14.3.6.3 Financials
      • 14.3.6.4 SWOT Analysis
    • 14.3.7 Invitae Corporation
      • 14.3.7.1 Company Overview
      • 14.3.7.2 Product Portfolio
      • 14.3.7.3 Financials
    • 14.3.8 Luminex Corporation (DiaSorin)
      • 14.3.8.1 Company Overview
      • 14.3.8.2 Product Portfolio
      • 14.3.8.3 SWOT Analysis
    • 14.3.9 Myriad Genetics Inc.
      • 14.3.9.1 Company Overview
      • 14.3.9.2 Product Portfolio
      • 14.3.9.3 Financials
      • 14.3.9.4 SWOT Analysis
    • 14.3.10 QIAGEN
      • 14.3.10.1 Company Overview
      • 14.3.10.2 Product Portfolio
      • 14.3.10.3 Financials
      • 14.3.10.4 SWOT Analysis
    • 14.3.11 Quest Diagnostics
      • 14.3.11.1 Company Overview
      • 14.3.11.2 Product Portfolio
      • 14.3.11.3 Financials
      • 14.3.11.4 SWOT Analysis
    • 14.3.12 Thermo Fisher Scientific
      • 14.3.12.1 Company Overview
      • 14.3.12.2 Product Portfolio
      • 14.3.12.3 Financials
      • 14.3.12.4 SWOT Analysis
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