시장보고서
상품코드
2024189

인간 유전자 시퀀싱 시장 : 용도별, 기술별, 워크플로우별, 제품별 및 국가별 전략, 동향, 예측 - 경영진용 가이드, 컨설턴트용 가이드 및 인공지능(AI)의 영향(2026-2030년)

Human Gene Sequencing Markets, Strategies & Trends. Forecasts by Application, by Technology, by Workflow, by Product, and by Country. With Executive and Consultant Guides and Impact of Artificial Intelligence. 2026 to 2030

발행일: | 리서치사: 구분자 Howe Sound Research | 페이지 정보: 영문 841 Pages | 배송안내 : 1-2일 (영업일 기준)

    
    
    



가격
PDF (Single User License) help
PDF 보고서를 1명(One device)만 이용할 수 있는 라이선스입니다. 인쇄 불가능하며 인쇄물의 이용 범위는 PDF 이용 범위와 동일합니다.
US $ 4,495 금액 안내 화살표 ₩ 6,803,000
PDF (Five User License) help
PDF 보고서를 동일 사업장의 5명(Five devices)까지 이용할 수 있는 라이선스입니다. 인쇄 불가능하며 인쇄물의 이용 범위는 PDF 이용 범위와 동일합니다.
US $ 6,495 금액 안내 화살표 ₩ 9,830,000
PDF (Enterprise License) help
PDF 보고서를 동일 기업의 모든 분이 이용할 수 있는 라이선스입니다. 인쇄는 가능하며 인쇄물의 이용 범위는 PDF 이용 범위와 동일합니다.
US $ 13,995 금액 안내 화살표 ₩ 21,181,000
카드담기
※ 부가세 별도
한글목차
영문목차
※ 본 상품은 영문 자료로 한글과 영문 목차에 불일치하는 내용이 있을 경우 영문을 우선합니다. 정확한 검토를 위해 영문 목차를 참고해주시기 바랍니다.

시장 개요:

인간 유전자 시퀀싱은 DNA 내 뉴클레오티드의 정확한 염기서열을 결정하기 위해 사용되는 일련의 기술을 말합니다. 이러한 기술을 통해 질병 위험, 치료 반응 및 생물학적 기능과 관련된 유전적 변이를 식별할 수 있습니다. 2003년 인간 유전체 프로젝트가 완료된 이후, 시퀀싱 기술의 발전으로 비용이 크게 절감되고 처리 능력이 향상되면서 유전자 시퀀싱은 전문 연구 활동에서 임상 진단, 의약품 개발 및 생물 의학 연구의 핵심 도구로 변모했습니다.

정밀의료, 종양학, 희귀질환 진단, 생식 건강 검진 및 약물유전체학 분야에서의 응용이 확대됨에 따라 전 세계 인간 유전자 시퀀싱 시장은 빠르게 성장하고 있습니다. 시장 규모는 2025년 115억 달러를 넘어 2030년까지 214억 달러에 달할 것으로 예상됩니다. 이는 13.1%의 성장률에 해당합니다. 차세대 염기서열 분석(NGS)은 수백만 개의 DNA 조각을 동시에 염기서열 분석할 수 있는 능력으로 인해 가장 큰 기술 분야를 차지하고 있습니다.

인간 유전자 시퀀싱 기술은 임상 의사결정 과정에 점점 더 많이 통합되고 있습니다. 염기서열 분석에 기반한 진단을 통해 암, 유전성 질환 및 치료 반응과 관련된 유전자 변이를 확인할 수 있습니다. 의료 시스템이 정밀의료 접근법을 채택함에 따라 유전자 시퀀싱은 현대 임상에서 필수적인 요소로 자리 잡고 있습니다.

기술의 진화

유전자 염기서열 분석 기술은 지난 20년 동안 눈부시게 발전했습니다. 1세대 시퀀싱 방법인 싱거법과 같은 1세대 시퀀싱 방법은 초기 유전체 연구에 널리 사용되었지만, 처리 능력이 상대적으로 낮고 샘플당 비용이 높다는 제약이 있었습니다.

차세대 시퀀싱 기술은 대부분의 응용 분야에서 1세대 기술을 거의 대체했습니다. NGS 플랫폼은 수백만 개의 DNA 조각을 동시에 시퀀싱할 수 있어 염기당 비용을 크게 낮추면서 종합적인 유전체 분석을 가능하게 합니다. NGS 기술은 전장유전체 시퀀싱(WGS), 전 엑솜 시퀀싱(WES), 표적 유전자 패널, 전사체 시퀀싱 등 다양한 용도를 지원하고 있습니다.

단분자 시퀀싱과 롱리드 시퀀싱을 포함한 3세대 시퀀싱 기술은 숏리드법으로는 분석이 어려운 구조적 변이 및 복잡한 유전체 영역을 검출할 수 있어 점점 더 많은 관심을 받고 있습니다. 롱 리드 시퀀싱 기술은 반복 서열 및 구조적 재구성의 분석 정확도를 향상시킵니다.

시퀀싱 워크플로우에는 일반적으로 샘플 조제, 라이브러리 구축, 시퀀싱 반응 및 생물정보학 분석이 포함됩니다. 자동화 기술과 클라우드 기반 바이오인포매틱스 툴의 발전으로 워크플로우의 효율성과 데이터 해석 능력이 향상되고 있습니다.

주요 응용 분야

인간 유전자 시퀀싱은 광범위한 임상 및 연구 분야에서 활용되고 있습니다.

종양학은 가장 큰 응용 분야 중 하나입니다. 시퀀싱 기술은 암의 발병 및 진행과 관련된 유전자 변이를 확인하기 위해 활용되고 있습니다. 분자 프로파일링을 통해 표적 치료제 선택을 유도할 수 있는 치료 가능한 돌연변이를 식별할 수 있습니다.

희귀 질환의 진단도 또 다른 중요한 응용 분야입니다. 많은 희귀질환은 유전적 요인으로 인해 발생하며, 시퀀싱 기술은 질병의 증상을 유발하는 병원성 돌연변이를 식별하는 데 도움이 됩니다.

비침습적 산전 검사(NIPT)는 산모의 혈액 속에 순환하는 무세포 태아 DNA의 염기서열을 분석하여 21번 삼염색체 등의 염색체 이상을 검출하는 검사입니다.

약물유전체학에서는 유전정보를 이용해 환자의 약물 반응을 예측하고, 용량 결정에 도움을 주고 있습니다.

감염성 질환 시퀀싱은 바이러스 및 세균성 병원체의 감시와 신종 변종 모니터링에 도움을 줍니다.

연구 용도에는 유전자 발견, 집단 유전체학, 진화 생물학, 바이오마커 식별 등이 포함됩니다.

시장 촉진요인

인간 유전자 시퀀싱 시장의 성장을 이끄는 몇 가지 요인이 있습니다.

  • 정밀의료(Precision Medicine) 접근법이 확대됨에 따라 맞춤형 치료 결정을 지원하는 유전체 정보에 대한 수요가 증가하고 있습니다.
  • 암 치료제 개발이 확대됨에 따라 치료 표적 발굴을 위한 염기서열 분석 기술의 활용이 증가하고 있습니다.
  • 대규모 집단 유전체 분석 이니셔티브는 하이스루풋 시퀀싱 기술에 대한 수요를 창출하고 있습니다.
  • 기술의 발전으로 시퀀싱 비용이 낮아지고, 이용 편의성이 향상되고 있습니다.
  • 유전체 검사를 도입한 임상 가이드라인이 확대되면서 보다 폭넓은 도입을 촉진하고 있습니다.
  • 바이오인포매틱스 도구의 활용도가 높아지면서 유전체 데이터 해석의 정확도가 향상되고 있습니다.

시장 세분화

인간 유전자 시퀀싱 시장은 기술 유형, 용도, 최종사용자 및 지역별로 세분화할 수 있습니다.

기술별로는 높은 처리량으로 인해 차세대 시퀀싱이 주요 부문을 차지하고 있습니다. 전장 유전체 시퀀싱, 전장 엑솜 시퀀싱 및 표적 유전자 패널이 중요한 응용 형태가 되고 있습니다.

용도별로는 NIPT(산전 검사)와 종양학이 가장 큰 비중을 차지하고 있습니다.

북미는 풍부한 연구 인프라와 높은 유전체 의료 보급률로 인해 가장 큰 지역 시장으로 자리매김하고 있습니다. 유럽과 아시아태평양 시장도 각국 정부의 유전체 연구 이니셔티브에 대한 투자로 확대되고 있습니다.

경쟁 상황

인간 유전자 시퀀싱 시장에는 장비 제조업체, 시약 공급업체, 시퀀싱 서비스 제공업체, 바이오인포매틱스 기업 등이 포함됩니다.

경쟁은 시퀀싱 정확도, 처리량, 비용 효율성, 데이터 분석 능력에 따라 좌우됩니다.

각 업체들은 시퀀싱 장비, 소모품, 바이오인포매틱스 소프트웨어를 결합한 통합 솔루션을 점점 더 많이 제공하고 있습니다.

시퀀싱 기술 제공업체와 제약회사와의 전략적 제휴는 특히 바이오마커 발굴 및 임상시험 분야에서 흔히 볼 수 있습니다.

데이터 해석 능력과 유전체 데이터베이스에 대한 접근성은 중요한 경쟁 차별화 요소가 되고 있습니다.

자본금 요건, 기술 전문성, 규제적 고려사항으로 인해 진입장벽은 여전히 높은 편입니다.

향후 전망

시퀀싱 기술이 의료 시스템 및 연구 프로그램에 점점 더 많이 통합됨에 따라 인간 유전자 시퀀싱 시장은 계속 확대될 것으로 예상됩니다.

시퀀싱 비용의 하락으로 전장유전체 시퀀싱의 도입이 증가할 것으로 예상됩니다.

인공지능과 바이오인포매틱스의 발전으로 유전체 데이터의 해석이 향상될 것으로 예상됩니다.

집단 유전체 분석의 노력으로 예방의학에서 시퀀싱 기술의 활용이 증가할 가능성이 있습니다.

유전체 데이터를 전자건강기록에 통합함으로써 맞춤형 의료 접근법을 지원할 수 있습니다.

새로운 롱리드 시퀀싱 기술은 구조적 변이 및 복잡한 유전체 특징의 검출 정확도를 향상시킬 수 있습니다.

전반적으로 인간 유전체 시퀀싱은 정밀의학, 생물의학 연구 및 신약개발을 뒷받침하는 기반 기술입니다. 지속적인 기술 혁신과 임상 적용 범위의 확대가 장기적인 시장 성장을 견인할 것으로 예상됩니다.

목차

제1장 시장 가이드

제2장 소개와 시장 정의

제3장 시퀸서 설치 상황 리스트 - 설치 장소와 연락처

제4장 시장 개요

제5장 시장 동향

제6장 인간 유전자 시퀀싱의 최근 동향

제7장 주요 기업 개요

제8장 세계의 인간 유전자 시퀀싱 시장

제9장 용도별 시장 규모

제10장 기술별 시장 규모

제11장 워크플로우별 시장 규모

제12장 제품별 시장 규모

제13장 인간 유전자 시퀀싱의 미래상

제14장 부록

표목차

그림목차

KSM 26.05.19

Market Overview:

Human gene sequencing refers to a group of technologies used to determine the precise order of nucleotides within DNA. These technologies enable identification of genetic variations associated with disease risk, treatment response, and biological function. Since completion of the Human Genome Project in 2003, advances in sequencing technologies have dramatically reduced cost and improved throughput, transforming gene sequencing from a specialized research activity into a core tool for clinical diagnostics, pharmaceutical development, and biomedical research.

The global human gene sequencing market has expanded rapidly as applications in precision medicine, oncology, rare disease diagnostics, reproductive health screening, and pharmacogenomics have grown. The market is over USD 11.5 Billion in 2025 and growing to 21.4 Billion by 2030. This represents a growth rate of 13.1%. Next-generation sequencing (NGS) represents the largest technology segments due to its ability to sequence millions of DNA fragments simultaneously.

Human gene sequencing technologies are increasingly integrated into clinical decision-making processes. Sequencing-based diagnostics enable identification of genetic mutations associated with cancer, inherited diseases, and treatment response. As healthcare systems adopt precision medicine approaches, gene sequencing is becoming an essential component of modern clinical practice.

Technology Evolution

Gene sequencing technologies have evolved significantly over the past two decades. First-generation sequencing methods, such as Sanger sequencing, were widely used for early genomic research but were limited by relatively low throughput and high cost per sample.

Next-generation sequencing technologies have largely replaced first-generation methods for most applications. NGS platforms allow simultaneous sequencing of millions of DNA fragments, enabling comprehensive genomic analysis at significantly lower cost per base. NGS technologies support a range of applications including whole genome sequencing (WGS), whole exome sequencing (WES), targeted gene panels, and transcriptome sequencing.

Third-generation sequencing technologies, including single-molecule and long-read sequencing methods, are gaining increasing attention due to their ability to detect structural variants and complex genomic regions that may be difficult to analyze using short-read methods. Long-read sequencing technologies provide improved characterization of repetitive sequences and structural rearrangements.

Sequencing workflows typically involve sample preparation, library construction, sequencing reactions, and bioinformatics analysis. Advances in automation and cloud-based bioinformatics tools have improved workflow efficiency and data interpretation capabilities.

Key Applications

Human gene sequencing is used across a wide range of clinical and research applications.

Oncology represents one of the largest application areas. Sequencing technologies are used to identify genetic mutations associated with cancer development and progression. Molecular profiling enables identification of actionable mutations that can guide targeted therapy selection.

Rare disease diagnostics represent another important application area. Many rare diseases have genetic origins, and sequencing technologies can help identify pathogenic variants responsible for disease symptoms.

Non-invasive prenatal testing (NIPT) uses sequencing of cell-free fetal DNA circulating in maternal blood to detect chromosomal abnormalities such as trisomy 21.

Pharmacogenomics uses genetic information to predict patient response to drugs and guide dosing decisions.

Infectious disease sequencing supports surveillance of viral and bacterial pathogens and monitoring of emerging variants.

Research applications include gene discovery, population genomics, evolutionary biology, and biomarker identification.

Market Drivers

Several factors are driving growth in the human gene sequencing market.

  • Increasing adoption of precision medicine approaches is creating demand for genomic information that supports personalized treatment decisions.
  • Growth in oncology drug development is increasing use of sequencing technologies to identify therapeutic targets.
  • Large population genomics initiatives are generating demand for high-throughput sequencing technologies.
  • Technological advances are reducing sequencing costs and improving accessibility.
  • Expansion of clinical guidelines incorporating genomic testing is supporting broader adoption.
  • Increasing availability of bioinformatics tools is improving interpretation of genomic data.

Market Segmentation

The human gene sequencing market can be segmented by technology type, application, end user, and geographic region.

By technology, next-generation sequencing represents the dominant segment due to high throughput capabilities. Whole genome sequencing, whole exome sequencing, and targeted gene panels represent important application formats.

By application, NIPT and Oncology represents the largest segments.

North America represents the largest geographic market due to strong research infrastructure and high adoption of genomic medicine. Europe and Asia-Pacific markets are also expanding as governments invest in genomic research initiatives.

Competitive Landscape

The human gene sequencing market includes instrument manufacturers, reagent suppliers, sequencing service providers, and bioinformatics companies.

Competition is driven by sequencing accuracy, throughput, cost efficiency, and data analysis capabilities.

Companies are increasingly offering integrated solutions combining sequencing instruments, consumables, and bioinformatics software.

Strategic partnerships between sequencing technology providers and pharmaceutical companies are common, particularly in biomarker discovery and clinical trial applications.

Data interpretation capabilities and access to genomic databases are becoming important competitive differentiators.

Barriers to entry remain significant due to capital requirements, technical expertise, and regulatory considerations.

Future Outlook

The human gene sequencing market is expected to continue expanding as sequencing technologies become more integrated into healthcare systems and research programs.

Declining sequencing costs are expected to increase adoption of whole genome sequencing.

Advances in artificial intelligence and bioinformatics are expected to improve interpretation of genomic data.

Population genomics initiatives may increase use of sequencing technologies in preventive medicine.

Integration of genomic data into electronic health records may support personalized treatment approaches.

Emerging long-read sequencing technologies may improve detection of structural variants and complex genomic features.

Overall, human gene sequencing represents a foundational technology supporting precision medicine, biomedical research, and drug development. Continued technological innovation and expanding clinical applications are expected to drive long-term market growth.

Table of Contents

1 Market Guides

  • 1.1 Human Gene Sequencing Markets - Strategic Situation Analysis
    • 1.1.1 Strategic Importance in Precision Medicine
    • 1.1.2 Cost Reduction and Economic Pressures
    • 1.1.3 Technology Innovation and Platform Competition
    • 1.1.4 Data Analysis and Bioinformatics Challenges
    • 1.1.5 Regulatory and Ethical Considerations
    • 1.1.6 Reimbursement and Clinical Adoption Barriers
    • 1.1.7 Competitive Landscape and Industry Structure
    • 1.1.8 Expansion of Clinical Applications
    • 1.1.9 Outlook and Strategic Implications
  • 1.2 Guide for Executives, Marketing, Sales and Business Development Staff
  • 1.3 Guide for Management Consultants and Investment Advisors
  • 1.4 Impact of Artificial Intelligence on Gene Sequencing Market

2 Introduction and Market Definition

  • 2.1 Gene Sequencing Definition In This Report
    • 2.1.1 Gene Sequencing
    • 2.1.2 Hereditary
    • 2.1.3 Non Invasive Prenatal Testing
    • 2.1.4 Oncology
    • 2.1.5 Psychology
    • 2.1.6 WGES
    • 2.1.7 Pharmacogenomic
    • 2.1.8 Direct to Consumer
    • 2.1.9 Research
    • 2.1.10 Other
  • 2.2 The Genomics Revolution
  • 2.3 Market Definition
    • 2.3.1 Revenue Market Size
  • 2.4 Methodology
    • 2.4.1 Methodology
    • 2.4.2 Sources
    • 2.4.3 Authors
  • 2.5 Perspective: Healthcare and the IVD Industry
    • 2.5.1 Global Healthcare Spending
    • 2.5.2 Spending on Diagnostics
    • 2.5.3 Important Role of Insurance for Diagnostics
  • 2.6 Chromosomes, Genes and Epigenetics
    • 2.6.1 Chromosomes
    • 2.6.2 Genes
    • 2.6.3 Epigenetics
    • 2.6.4 Genetic Testing vs. Gene Sequencing
    • 2.6.5 Cost and Pricing Practice

3 Global Listing of Sequencer Installed Base - Location & Contacts

  • 3.1 Notes to Installed Base Listing
  • 3.2 Illumina Installed Base

4 Market Overview

  • 4.1 Players in a Dynamic Market
    • 4.1.1 Academic Research Lab
    • 4.1.2 Diagnostic Test Developer
    • 4.1.3 Instrumentation Supplier
    • 4.1.4 Chemical/Reagent Supplier
    • 4.1.5 Pathology Supplier
    • 4.1.6 Independent Clinical Laboratory
    • 4.1.7 Public National/regional Laboratory
    • 4.1.8 Hospital Laboratory
    • 4.1.9 Physicians Office Lab (POLS)
    • 4.1.10 Audit Body
    • 4.1.11 Certification Body
  • 4.2 Human Gene Sequencing - Markets, Examples and Discussion
    • 4.2.1 Inherited Disease - Not what it used to be
      • 4.2.1.1 Clinical and Research Lines Blur
      • 4.2.1.2 Genetic Counselling - Not so simple anymore
      • 4.2.1.3 The Genetic Blizzard - Issues of Access and Payment
    • 4.2.2 Newborn Screening - The Standard of Care
      • 4.2.2.1 Newborn Screening - Do Parents Want to Know?
    • 4.2.3 NIPT - We've Only Just Begun
      • 4.2.3.1 NIPT, IVF and the Fertility Practice - PGS, PGD, CCS
      • 4.2.3.2 NIPT in the Future - Beyond Inherited Disease
    • 4.2.4 Oncology - Understanding Two Worlds
      • 4.2.4.1 The Tumor - A Sequence of Sequencing
      • 4.2.4.2 The Tumor - Biopsy and Liquid Biopsy
      • 4.2.4.3 The Human Genome - Predisposition and Prognosis
    • 4.2.5 Pharmacogenomics
      • 4.2.5.1 Sequencing Not the Only Player
      • 4.2.5.2 New Roles for Old Drugs - A Research Bonanza?
    • 4.2.6 Direct To Consumer - More Than Meets the Eye
      • 4.2.6.1 DTC - How Many Segments?
  • 4.3 Industry Structure
    • 4.3.1 Hospital's Testing Share
    • 4.3.2 The Rise of the Sequencing Lab
    • 4.3.3 Sequencing as a Commodity
    • 4.3.4 Informatics
    • 4.3.5 Instrument Manufacturer Role
    • 4.3.6 Healthcare Industry Impacts - Still Struggling
    • 4.3.7 Can the Healthcare Industry Adapt?
    • 4.3.8 Genetic Counselling as an Industry
    • 4.3.9 Sequencing Adoption and Cannibalization

5 Market Trends

  • 5.1 Factors Driving Growth
    • 5.1.1 New Diagnoses
    • 5.1.2 Wellness and Prevention
    • 5.1.3 Fertility Technology
    • 5.1.4 Cancer - Screening, Management and Monitoring
  • 5.2 Factors Limiting Growth
    • 5.2.1 Increased Competition Lowers Price
    • 5.2.2 Lower Costs
    • 5.2.3 Healthcare Cost Concerns Curtail Growth
    • 5.2.4 Wellness has a downside
  • 5.3 Sequencing Instrumentation
    • 5.3.1 Instrumentation Tenacity
    • 5.3.2 Declining Cost of Instruments Changes Industry Structure
    • 5.3.3 Long Reads - Further Segmentation
    • 5.3.4 Linked Reads
    • 5.3.5 New Sequencing Technologies

6 Human Gene Sequencing Recent Developments

  • 6.1 Recent Developments - Importance and How to Use This Section
    • 6.1.1 Importance of These Developments
    • 6.1.2 How to Use This Section
  • 6.2 Adaptive Biotechnologies MRD Testing Grows
  • 6.3 GeneDx to Acquire Fabric Genomics
  • 6.4 Inclusive Newborn Sequencing Shows Potential
  • 6.5 Delve Bio: Delve Detect
  • 6.6 Caris CDx Assay Approval
  • 6.7 Ambry Genetics: ExomeReveal
  • 6.8 WGS Improves Pediatric Cancer Care
  • 6.9 Cancer genomes identify candidate driver genes
  • 6.10 Genetic Dx a game changer
  • 6.11 Nonacus Galeas Tumor
  • 6.12 Lucence LiquidHallmark Assay Gets Coverage
  • 6.13 Garvan Institute Gets Gramt to Develop Genomics Tests
  • 6.14 Arima Genomics, Protean BioDiagnostics Launch Joint Venture
  • 6.15 Geneseeq Nabs CE Marks for Cancer Test Kits
  • 6.16 Viome Life Sciences Announces Gut Intelligence Test
  • 6.17 Quest Diagnostics Announces Genetic Insights
  • 6.18 Exact Sciences Releases Next-Gen Cologuard
  • 6.19 BGI Genomics Forges Partnerships in Latin America
  • 6.20 4bases Bets on NGS Diagnostics
  • 6.21 Guardant Health Submits Colorectal Cancer Screening Test
  • 6.22 Universal DX Eyeing Approval for Colorectal Cancer Screening Test
  • 6.23 Natera Files Suit Against NeoGenomics
  • 6.24 Genomics England to Sequence 100K Newborns
  • 6.25 Novigenix Raises $14M for NGS based Liquid Biopsy
  • 6.26 LetsGetChecked Launching New PGx Service
  • 6.27 Qiagen, Neuron23 Partner for NGS Diagnostic
  • 6.28 Harbinger Health Technology Focused On Oncogenesis
  • 6.29 Delfi Diagnostics to Develop Early Detection Test
  • 6.30 Dante Labs to Introduce WGS to Italian Healthcare System
  • 6.31 Invitae Neurodevelopmental Disorders Testing Service
  • 6.32 Thermo Fisher Obtains CE Mark for Ion Torrent Genexus
  • 6.33 Myriad Genetics Launches Suite of Cancer Tests
  • 6.34 Oncocyte and Thermo Fisher Strike Partnership Deal
  • 6.35 Illumina Partners With Precision Medicine to Assess Liquid Biopsy
  • 6.36 Sysmex Inostics Develops Ultra-Sensitive Liquid Biopsy
  • 6.37 Twist Bioscience, Centogene Partner on NGS-Based Rare Disease Testing
  • 6.38 Strata Oncology Trial Supports NGS Assay
  • 6.39 NYU Gets FDA Clearance for Sequencing Test
  • 6.40 NeoGenomics to Acquire Inivata
  • 6.41 OncoDNA, Institut Curie Partner on Liquid Biopsy Research
  • 6.42 Cancer Heritability Gene Set Expanded
  • 6.43 Whole-Genome Sequencing Could Replace Cytogenetics
  • 6.44 Twist Bioscience, Berry Genomics Partner on Targeted NGS Assays
  • 6.45 Ancestry Shutters Health Offering
  • 6.46 Genetron Health Targeting Early Cancer Detection
  • 6.47 Pan-European Initiative to Build Tools for Sharing Genomic Data
  • 6.48 UK Government Unveils New Genomic Healthcare Strategy
  • 6.49 Foundation Medicine Liquid Biopsy Gets FDA Approval
  • 6.50 American Heart Association Develops Genetic Testing Guidelines
  • 6.51 Yourgene Health Gets CE Mark for Iona NIPT Test
  • 6.52 NorthShore Looks to Expand Genomics Integration Into Primary Care
  • 6.53 Germline Results From Tumor Sequencing Guides Precision Therapy
  • 6.54 FDA Clears Cancer Genomic Profiling From Personal Genome Diagnostics
  • 6.55 BillionToOne Closes $15M Series A Follow-on Round
  • 6.56 Clinics to Integrate Genomics Into Primary Care

7 Profiles of Key Companies

  • 7.1 10x Genomics, Inc.
  • 7.2 23andME Inc.
  • 7.3 Abbott Laboratories
  • 7.4 AccuraGen Inc.
  • 7.5 Adaptive Biotechnologies
  • 7.6 Admera Health, LLC
  • 7.7 Advanced Biological Laboratories
  • 7.8 Agilent
  • 7.9 Akonni Biosystems
  • 7.10 Amoy Diagnostics Co., Ltd.
  • 7.11 Ancestry.com LLC
  • 7.12 Anchor Dx
  • 7.13 Arrayit Corporation
  • 7.14 ARUP Laboratories
  • 7.15 Astrid Bio
  • 7.16 Azenta
  • 7.17 BaseClear
  • 7.18 Baylor Miraca Genetics Laboratories
  • 7.19 Beckman Coulter Diagnostics (Danaher)
  • 7.20 Becton, Dickinson and Company
  • 7.21 BGI Genomics Co. Ltd
  • 7.22 Bioarray Genetics
  • 7.23 BioBam
  • 7.24 Biocept, Inc.
  • 7.25 Biodesix Inc.
  • 7.26 BioFluidica
  • 7.27 BioGenex
  • 7.28 Biolidics Ltd
  • 7.29 bioMerieux Diagnostics
  • 7.30 Bioneer Corporation
  • 7.31 Bio-Rad Laboratories, Inc.
  • 7.32 Bio-Techne
  • 7.33 Burning Rock
  • 7.34 C2i Genomics
  • 7.35 Cantata Bio
  • 7.36 CareDx
  • 7.37 Caris Molecular Diagnostics
  • 7.38 Celemics
  • 7.39 CellMax Life
  • 7.40 Centogene
  • 7.41 Cepheid (Danaher)
  • 7.42 Circulogene
  • 7.43 Clearbridge Biomedics
  • 7.44 Clinical Genomics
  • 7.45 Color Genomics
  • 7.46 Complete Genomics (MGI Tech)
  • 7.47 CosmosID
  • 7.48 Dante Labs
  • 7.49 Datar Cancer Genetics Limited
  • 7.50 Diasorin S.p.A.
  • 7.51 Easy DNA
  • 7.52 Element Biosciences
  • 7.53 Epic Sciences
  • 7.54 Epigenomics AG
  • 7.55 Eurofins Scientific
  • 7.56 Excellerate Bioscience
  • 7.57 Fabric Genomics
  • 7.58 Freenome
  • 7.59 FUJIFILM Wako Diagnostics
  • 7.60 Fujirebio
  • 7.61 Fulgent Genetics
  • 7.62 GE Global Research
  • 7.63 Gene by Gene, Ltd.
  • 7.64 Genedrive
  • 7.65 GeneDx Holdings
  • 7.66 GeneFirst Ltd.
  • 7.67 GeneFluidics
  • 7.68 Genetron Holdings
  • 7.69 Genewiz
  • 7.70 Genomics England
  • 7.71 Genomics Personalized Health (GPH)
  • 7.72 GenomOncology
  • 7.73 Genzyme Corporation
  • 7.74 Grifols
  • 7.75 Guardant Health
  • 7.76 Guardiome
  • 7.77 Helix
  • 7.78 Hologic
  • 7.79 HTG Molecular Diagnostics
  • 7.80 Human Longevity, Inc.
  • 7.81 iCellate
  • 7.82 Illumina
  • 7.83 Incell Dx
  • 7.84 Inivata
  • 7.85 Invitae Corporation
  • 7.86 Invivoscribe
  • 7.87 Karius
  • 7.88 Letsgetchecked
  • 7.89 Lucence Health
  • 7.90 Lunglife AI Inc
  • 7.91 Macrogen
  • 7.92 MDNA Life SCIENCES, Inc.
  • 7.93 MDx Health
  • 7.94 Medgenome
  • 7.95 Meridian Bioscience
  • 7.96 Mesa Laboratories, Inc.
  • 7.97 Metabiomics Corp
  • 7.98 miR Scientific
  • 7.99 NantHealth, Inc.
  • 7.100 Natera
  • 7.101 Nebula Genomics
  • 7.102 NeoGenomics
  • 7.103 New England Biolabs, Inc.
  • 7.104 NGeneBio
  • 7.105 Norgen Biotek Corp.
  • 7.106 Novogene
  • 7.107 Omega Bioservices
  • 7.108 Oncocyte
  • 7.109 OncoDNA
  • 7.110 OpGen
  • 7.111 Origene Technologies
  • 7.112 Oxford Nanopore Technologies
  • 7.113 Pacific Biosciences
  • 7.114 Panagene
  • 7.115 PathoQuest S.A.
  • 7.116 Personalis
  • 7.117 PGDx (Labcorp)
  • 7.118 Precipio
  • 7.119 PrecisionMed
  • 7.120 Predictive Oncology
  • 7.121 Promega
  • 7.122 Qiagen
  • 7.123 QuantuMDx
  • 7.124 Regeneron Pharmaceuticals
  • 7.125 Revvity
  • 7.126 Roche Diagnostics
  • 7.127 Roswell Biotechnologies
  • 7.128 Seegene
  • 7.129 SeLux Diagnostics
  • 7.130 Sequencing.com
  • 7.131 Siemens Healthineers
  • 7.132 simfo GmbH
  • 7.133 Singlera Genomics Inc.
  • 7.134 Singular Genomics
  • 7.135 SkylineDx
  • 7.136 Standard BioTools
  • 7.137 Sysmex
  • 7.138 Sysmex Inostics
  • 7.139 Tempus Labs, Inc.
  • 7.140 Thermo Fisher Scientific
  • 7.141 Ultima Genomics
  • 7.142 Unchained Labs
  • 7.143 Variantyx
  • 7.144 Vela Diagnostics
  • 7.145 VolitionRX
  • 7.146 Zymo Research Corp

8 The Global Market for Human Genome Sequencing

  • 8.1 Global Market Overview by Country
    • 8.1.1 Table - Global Market by Country
    • 8.1.2 Chart - Global Market by Country
  • 8.2 Global Market by Application - Overview
    • 8.2.1 Table - Global Market by Application
    • 8.2.2 Chart - Global Market by Application - Base/Final Year Comparison
    • 8.2.3 Chart - Global Market by Application - Base Year
    • 8.2.4 Chart - Global Market by Application - Final Year
    • 8.2.5 Chart - Global Market by Application - Share by Year
    • 8.2.6 Chart - Global Market by Application - Segment Growth
  • 8.3 Global Market by Technology - Overview
    • 8.3.1 Table - Global Market by Technology
    • 8.3.2 Chart - Global Market by Technology - Base/Final Year Comparison
    • 8.3.3 Chart - Global Market by Technology - Base Year
    • 8.3.4 Chart - Global Market by Technology - Final Year
    • 8.3.5 Chart - Global Market by Technology - Share by Year
    • 8.3.6 Chart - Global Market by Technology - Segment Growth
  • 8.4 Global Market by Workflow - Overview
    • 8.4.1 Table - Global Market by Workflow
    • 8.4.2 Chart - Global Market by Workflow - Base/Final Year Comparison
    • 8.4.3 Chart - Global Market by Workflow - Base Year
    • 8.4.4 Chart - Global Market by Workflow - Final Year
    • 8.4.5 Chart - Global Market by Workflow - Share by Year
    • 8.4.6 Chart - Global Market by Workflow - Segment Growth
  • 8.5 Global Market by Product - Overview
    • 8.5.1 Table - Global Market by Product
    • 8.5.2 Chart - Global Market by Product - Base/Final Year Comparison
    • 8.5.3 Chart - Global Market by Product - Base Year
    • 8.5.4 Chart - Global Market by Product - Final Year
    • 8.5.5 Chart - Global Market by Product - Share by Year
    • 8.5.6 Chart - Global Market by Product - Segment Growth

9 Market Sizes by Application

  • 9.1 Hereditary Gene Sequencing Market
    • 9.1.1 Table - Hereditary by Country
    • 9.1.2 Chart - Hereditary Segment Growth
  • 9.2 NIPT Gene Sequencing Market
    • 9.2.1 Table NIPT by Country
    • 9.2.2 Chart - NIPT Growth
  • 9.3 Oncology Market
    • 9.3.1 Table - Oncology by Country
    • 9.3.2 Chart - Oncology Growth
  • 9.4 Psychology Market
    • 9.4.1 Table - Psychology by Country
    • 9.4.2 Chart - Psychology Growth
  • 9.5 WGES Gene Sequencing Market
    • 9.5.1 Table - WGES by Country
    • 9.5.2 Chart - WGES growth
  • 9.6 Pharmacogenomics Market
    • 9.6.1 Table Pharmacogenomics by Country
    • 9.6.2 Chart - Pharmacogenomics Growth
  • 9.7 DTC Gene Sequencing Market
    • 9.7.1 Table - DTC by Country
    • 9.7.2 Chart - DTC Growth
  • 9.8 Research Gene Sequencing Market
    • 9.8.1 Table - Research by Country
    • 9.8.2 Chart - Research Growth
  • 9.9 Other Application Market
    • 9.9.1 Table - Other Application by Country
    • 9.9.2 Chart - Other Application growth

10 Market Sizes by Technology

  • 10.1 Sanger Sequencing Market
    • 10.1.1 Table - Sanger by Country
    • 10.1.2 Chart - Sanger Segment Growth
  • 10.2 NGS/2G Market
    • 10.2.1 Table NGS/2G by Country
    • 10.2.2 Chart - NGS/2G Growth
  • 10.3 3G/Long Market
    • 10.3.1 Table - 3G/Long by Country
    • 10.3.2 Chart - 3G/Long Growth
  • 10.4 Other Technology Market
    • 10.4.1 Table - Other Technology by Country
    • 10.4.2 Chart - Other Technology Growth

11 Market Sizes by Workflow

  • 11.1 Sequencing Market
    • 11.1.1 Table - Sequencing by Country
    • 11.1.2 Chart - Sequencing Segment Growth
  • 11.2 Sample Prep Market
    • 11.2.1 Table Sample Prep by Country
    • 11.2.2 Chart - Sample Prep Growth
  • 11.3 Analysis Market
    • 11.3.1 Table - Analysis by Country
    • 11.3.2 Chart - Analysis Growth

12 Market Sizes by Product

  • 12.1 Instruments Market
    • 12.1.1 Table - Instruments by Country
    • 12.1.2 Chart - Instruments Segment Growth
  • 12.2 Consumables Market
    • 12.2.1 Table Consumables by Country
    • 12.2.2 Chart - Consumables Growth
  • 12.3 Software & Services Market
    • 12.3.1 Table - Software & Services by Country
    • 12.3.2 Chart - Software & Services Growth

13 Vision of the Future of Human Gene Sequencing

14 Appendices

  • 14.1 Growth of Approved IVD Test Menu
  • 14.2 Growth of Approved Average IVD Test Fee
  • 14.3 The Most Used IVD Assays
  • 14.4 The Highest Grossing Assays
  • 14.5 Laboratory Fees Schedule
  • 14.6 The Whole Genome Sequence of SARS-CoV-2

Table of Tables

  • Table 1 The Base Pairs
  • Table 2 Most Common Traditional Genetic Disorders
  • Table 3 The Base Pairs
  • Table 4 List of GLOBAL SEQUENCING LOCATIONS
  • Table 5 Market Players by Type
  • Table 6 The Different Markets for Human Gene Sequencing
  • Table 7 DTC Sub Segments
  • Table 8 The Factors Driving Growth
  • Table 9 Factors Limiting Growth
  • Table 10 Six New Sequencing Technologies
  • Table 11 - Global Market by Region
  • Table 12 Global Market by Application
  • Table 13 Global Market by Technology
  • Table 14 Global Market by Workflow
  • Table 15 Global Market by Product
  • Table 16 Hereditary Segment by Country
  • Table 17 NIPT Segment by Country
  • Table 18 Oncology Segment by Country
  • Table 19 Psychology Segment by Country
  • Table 20 WGES Segment by Country
  • Table 21 Pharmacogenomics Segment by Country
  • Table 22 DTC Segment by Country
  • Table 23 Research Segment by Country
  • Table 24 Other Application Segment by Country
  • Table 25 Sanger Segment by Country
  • Table 26 NGS/2G Segment by Country
  • Table 27 3G/Long Segment by Country
  • Table 28 Other Technology by Country
  • Table 29 Sequencing Segment by Country
  • Table 30 Sample Prep Segment by Country
  • Table 31 Analysis Segment by Country
  • Table 32 Instruments Segment by Country
  • Table 33 Consumables Segment by Country
  • Table 34 Software & Services Segment by Country
  • Table 35 The Most Common Assays
  • Table 36 Largest Revenue Assays
  • Table 37 Clinical Lab Fee Schedule

Table of Figures

  • Figure 1 Global Healthcare Spending
  • Figure 2 The Lab Test Pie
  • Figure 3 DNA Strands and Chromosomes
  • Figure 4 Karyogram of Human Chromosomes
  • Figure 5 Size of Various Genomes
  • Figure 6 Global Illumina Installed Base Map
  • Figure 7 The Road to Diagnostics
  • Figure 8 TruSight Germline Panel
  • Figure 9 Historical Cost of Gene Sequencing
  • Figure 10 - Cost To Sequence a Human Genome
  • Figure 11 Base Year Country Market Share Chart
  • Figure 12 Global Market by Application - Base vs. Final Year
  • Figure 13 Global Market by Application Base Year
  • Figure 14 Global Market by Application Final Year
  • Figure 15 Application Type Share by Year
  • Figure 16 by Application Segment Growth
  • Figure 17 Global Market by Technology - Base vs. Final Year
  • Figure 18 Global Market by Technology Base Year
  • Figure 19 Global Market by Technology Final Year
  • Figure 20 Technology Type Share by Year
  • Figure 21 by Technology Segment Growth
  • Figure 22 Global Market by Workflow - Base vs. Final Year
  • Figure 23 Global Market by Workflow Base Year
  • Figure 24 Global Market by Workflow Final Year
  • Figure 25 Workflow Type Share by Year
  • Figure 26 by Workflow Segment Growth
  • Figure 27 Global Market by Product - Base vs. Final Year
  • Figure 28 Global Market by Product Base Year
  • Figure 29 Global Market by Product Final Year
  • Figure 30 Product Type Share by Year
  • Figure 31 by Product Segment Growth
  • Figure 32 Hereditary vs. Total Market Growth
  • Figure 33 NIPT vs. Total Market Growth
  • Figure 34 Oncology vs. Total Market Growth
  • Figure 35 Psychology vs. Total Market Growth
  • Figure 36 WGES vs. Total Market Growth
  • Figure 37 Pharmacogenomics vs. Total Market Growth
  • Figure 38 DTC vs. Total Market Growth
  • Figure 39 Research vs. Total Market Growth
  • Figure 40 Other Application vs. Total Market Growth
  • Figure 41 Sanger vs. Total Market Growth
  • Figure 42 NGS/2G vs. Total Market Growth
  • Figure 43 3G/Long vs. Total Market Growth
  • Figure 44 Other Technology vs. Total Market Growth
  • Figure 45 Sequencing vs. Total Market Growth
  • Figure 46 Sample Prep vs. Total Market Growth
  • Figure 47 Analysis vs. Total Market Growth
  • Figure 48 Instruments vs. Total Market Growth
  • Figure 49 Consumables vs. Total Market Growth
  • Figure 50 Software & Services vs. Total Market Growth
  • Figure 51 IVD Test Menu Growth
  • Figure 52 IVD Test Average Fees - A Ten Year View
샘플 요청 목록
0 건의 상품을 선택 중
목록 보기
전체삭제
문의
원하시는 정보를
찾아 드릴까요?
문의주시면 필요한 정보를
신속하게 찾아드릴게요.
02-2025-2992
kr-info@giikorea.co.kr
문의하기