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市場調查報告書
次世代定序：基因組解析
Next-Generation Sequencing: Solving the Genome
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次世代定序：基因組解析 是由出版商Insight Pharma Reports在2009年06月所出版的。
這份英文市場調查報告書包含164 Pages 價格從美金3195起跳。
此報告書彙整了目前的次世代定序平台動向、市場以及競爭環境、開發中系統、生物資訊學、次世代定序應用等。報告書之內容摘要如下所示。
第1章 說明
第2章 定序技術的歷史與展開
- Ferdrick Sanger與早期DNA定序
- Leroy Hood Pioneers的半自動定序
- 人類基因組計畫與Celera Genomics
- 1000美金基因組與次世代系統
第3章 定序技術：次世代
- 目前的次世代定序器
- 開發中的定序器
- 使用奈米孔道的系統
- 性能比較
- 生物資訊學
- 樣品準備
- National Human Genome Research Institute (NHGRI)基金
- 智慧財產問題
第4章 次世代定序技術的應用
- 全基因組計畫
- RNA定序
- 基因規定與管理分析
- 疾病診斷與預測
- 宏基因組
第5章 市場動向
第6章 觀察與結論
第7章 訪談
參考
附網址的企業目錄
Abstract
Next-generation sequencing (NGS) technologies are advancing in quality and
applications diversity at a breathtaking pace. The market is diversifying
strongly into labs without previous involvement in sequencing.
This report examines:
- Current NGS platforms and how they compare
- Market dynamics and competitive landscape for new entrants
- Next-generation systems in development
- Bioinformatics issues
- Applications of NGS
- User survey results and views of interviewees
The first generation of DNA sequencing can be said to have ended when the
first few human genomes were sequenced and a large number of genetic
variations were detected in a relatively few individuals. Sequencing
throughput is rising dramatically as costs per unit of sequence are falling
equally dramatically. Now it has become possible to sequence a sufficiently
large number of human genomes to explore the extent and medical meaning of
genetic variations in statistically meaningful ways. The race to the "$1,000
genome" is well underway, and the number of entrants is surprisingly large, as
are the ingenuity and inventiveness that have been brought to race.
Next-Generation Sequencing: Solving the Genome provides a detailed overview of
the technologies involved in next-generation sequencing, starting with the
four systems currently on the market and continuing with those now in
development. A number of companies have technologies that promise some
advantage over existing systems, but whether those advantages will be great
enough to merit significant market share remains an open question. We also
provide an overview of bioinformatics issues in next-generation sequencing and
a comparative analysis of currently available platforms.
Applications of next-generation sequencing discussed in this report include
whole-genome sequencing, RNA resequencing, ChIP-seq, disease prediction and
diagnosis, and personal genomics. Next-generation sequencing is starting to
impinge on DNA microarray usage and should continue to do so as costs drop.
Existing next-generation sequencing users are striving to expand the case for
personal genomics and for personalized medicine in general. Next-generation
systems are currently enabling the genome-wide association studies needed to
identify the genome variants central to deeper understanding of the molecular
basis of genetically complex diseases and predicting individual risk of
developing them.
Next-Generation Sequencing: Solving the Genome examines market dynamics and
includes discussions of key issues relating to the competitive position of
various technologies and companies. Next-generation sequencing instruments and
consumables are selling rapidly and contributing nicely to growth rates of the
market leaders. Second-round players must offer significant improvements over
current market entrants in order to merit viable market share. Third-round
technologies, particularly those involving nanopores, remain speculative at
present, but could serve to accelerate market decentralization by virtue of
extremely low costs and high speeds.
An Insight Pharma survey of next-generation sequencing system users generated
a number of interesting observations and opinions, which are discussed.
Transcripts from extended interviews with scientists and managers
knowledgeable in the field are also included.
Table of Contents
Chapter 1 INTRODUCTION
- 1.1. Background
- 1.2. Scope and Nature of the Report
Chapter 2 HISTORY AND EVOLUTION OF SEQUENCING TECHNOLOGY
- 2.1. Frederick Sanger & Early DNA Sequencing
- 2.2. Leroy Hood Pioneers Semi-Automated Sequencing
- 2.3. The Human Genome Project and Celera Genomics: Race On
- 2.4. The $1,000 Genome & Next-Generation Systems
Chapter 3 SEQUENCING TECHNOLOGIES: NEXT-GENERATION AND BEYOND
- 3.1. Current Next-Generation Sequencers
- Roche/454 Life Sciences
- Illumina
- Applied Biosystems
- Helicos
- 3.2. Sequencers Currently in Development
- Complete Genomics
- BioNanomatrix
- VisiGen
- Pacific Biosciences
- Dover Systems
- Intelligent Bio-Systems
- ZS Genetics
- Reveo
- LightSpeed Genomics
- 3.3. Nanopore-Based Systems
- NABsys
- Oxford Nanopore Technologies
- 3.4. Performance Comparisons
- 3.5. Bioinformatics
- 3.6. Sample Preparation
- 3.7. National Human Genome Research Institute (NHGRI) Funding
- 3.8. Intellectual Property Issues
Chapter 4 APPLICATIONS OF NEXT-GENERATION SEQUENCING TECHNOLOGIES
- 4.1. Whole-Genome Sequencing
- The 1,000 Genomes Project
- Exon Sequencing
- Accuracy and Precision in Genetic Variation Studies
- 4.2. RNA Sequencing
- 4.3. Gene Regulation and Control Analysis
- 4.4. Disease Diagnosis and Prediction
- Cancer Genomics
- Personal Genomics
- 4.5. Metagenomics
Chapter 5 MARKET DYNAMICS
- 5.1. Deals
- 5.2. User Survey Results
- Chief Application for Next-Generation DNA Sequencing
- Main Organism for Next-Generation Sequencing
- User Experience with Next-Generation Platform, Industry Segment
- Next-Generation Platform Predicted to Dominate in 2 - 3 Years
- Most Exciting Third-Generation Platform
- Applications to Benefit Most from Next-Generation Sequencing
- Research Areas to Benefit Most from Next-Generation Sequencing
- Greatest Technical Concern about Next-Generation Sequencing Platforms
- Greatest Computational/IT Concern
- Adequate Cost/Benefit from Next-Generation Sequencing
- Cost of Full Human Genome Sequence by 2010
- Opinion on Platform Market Dominance
- Future of Sanger Sequencing
- Most Important Factors in Selecting a Next-Generation System
- Opinion on Acquiring Sequence from a Service Provider
- 5.3. The Competitive Environment
Chapter 6 OBSERVATIONS AND CONCLUSIONS
Chapter 7 INTERVIEW TRANSCRIPTS
- 7.1. Clifford Reid, PhD, Chairman, President, & CEO, Complete Genomics
- 7.2. Patrice Milos, PhD, VP & Chief Scientific Officer, Helicos BioSciences
- 7.3. Steven Salzberg, PhD, Director, Center for Bioinformatics and
Computational Biology, University of Maryland
- 7.4. Todd Smith, PhD, Chief Science Officer, Geospiza
- 7.5. Anonymous Academic Researcher Active in Next-Generation Sequencing
- 7.6. Stephen Naylor, PhD, CSO & Chairman, Predictive Physiology and
Medicine (PPM)
References
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