Difference between revisions of "Guide to Analysis of DNA Microarray Data"

Latest revision as of 12:34, 5 January 2006

Guide to Analysis of DNA Microarray Data (ISBN 047165604) by Steen Knudsen.

Bibliography

• Paperback: 184 pages
• Publisher: Wiley-Liss; 2nd Edition; 2 March 2004
• Language: English
• ISBN: 0471656046

Table of Contents

• Preface
• Acknowledgments
• 1. Introduction to DNA Microarray Technology
  • 1.1 Hybridization.
  • 1.2 Gold Rush?
  • 1.3 The Technology behind DNA Microarrays
    • 1.3.1 Affymetrix GeneChip Technology
    • 1.3.2 Spotted Arrays
    • 1.3.3 Digital Micromirror Arrays
    • 1.3.4 Inkjet Arrays
    • 1.3.5 Bead Arrays
    • 1.3.6 Serial Analysis of Gene Expression (SAGE)
  • 1.4 Parallel Sequencing on Microbead Arrays
    • 1.4.1 Emerging Technologies
  • 1.5 Example: Affymetrix vs. Spotted Arrays
  • 1.6 Summary
  • 1.7 Further Reading
• 2. Overview of Data Analysis
• 3. Image Analysis
  • 3.1 Gridding
  • 3.2 Segmentation
  • 3.3 Intensity Extraction
  • 3.4 Background Correction
  • 3.5 Software
    • 3.5.1 Free Software for Array Image Analysis
    • 3.5.2 Commercial Software for Array Image Analysis
  • 3.6 Summary
  • 3.7 Further Reading
• 4. Basic Data Analysis
  • 4.1 Normalization
    • 4.1.1 One or More Genes are Assumed Expressed at Constant Rate
    • 4.1.2 Sum of Genes is Assumed Constant
    • 4.1.3 Subset of Genes is Assumed Constant
    • 4.1.4 Majority of Genes Assumed Constant
    • 4.1.5 Spike Controls
  • 4.2 Dye Bias, Spatial Bias, Print Tip Bias
  • 4.3 Expression Indices
    • 4.3.1 Average Difference
    • 4.3.2 Signal
    • 4.3.3 Model-Based Expression Index
    • 4.3.4 Robust Multiarray Average
    • 4.3.5 Position Dependent Nearest Neighbor Model
  • 4.4 Detection of Outliers
  • 4.5 Fold Change
  • 4.6 Significance
    • 4.6.1 Multiple Conditions
    • 4.6.2 Nonparametric Tests
    • 4.6.3 Correction for Multiple Testing
    • 4.6.4 Example I: t-Test and ANOVA
    • 4.6.5 Example II: Number of Replicates
  • 4.7 Mixed Cell Populations
  • 4.8 Summary
  • 4.9 Further Reading
• 5. Visualization by Reduction of Dimensionality
  • 5.1 Principal Component Analysis
  • 5.2 Example 1: PCA on Small Data Matrix
  • 5.3 Example 2: PCA on Real Data
  • 5.4 Summary
  • 5.5 Further Reading
• 6. Cluster Analysis
  • 6.1 Hierarchical Clustering
  • 6.2 K-means Clustering
  • 6.3 Self-Organizing Maps
  • 6.4 Distance Measures
    • 6.4.1 Example: Comparison of Distance Measures
  • 6.5 Gene Normalization
  • 6.6 Visualization of Clusters
    • 6.6.1 Example: Visualization of Gene Clusters in Bladder Cancer
  • 6.7 Summary
  • 6.8 Further Reading
• 7. Beyond Cluster Analysis
  • 7.1 Function Prediction
  • 7.2 Discovery of Regulatory Elements in Promoter Regions
    • 7.2.1 Example 1: Discovery of Proteasomal Element
    • 7.2.2 Example 2: Rediscovery of Mlu Cell Cycle Box (MCB)
  • 7.3 Summary
  • 7.4 Further Reading
• 8. Automated Analysis, Integrated Analysis and Systems Biology
  • 8.1 Integrated Analysis
  • 8.2 Systems Biology
  • 8.3 Further Reading
• 9. Reverse Engineering of Regulatory Networks
  • 9.1 The Time-Series Approach
  • 9.2 The Steady-State Approach
  • 9.3 Limitations of Network Modeling
  • 9.4 Example 1: Steady-State Model
  • 9.5 Example 2: Steady-State Model on Bacillus Data
  • 9.6 Example 3: Linear Time-Series Model
  • 9.7 Further Reading
• 10. Molecular Classifiers
  • 10.1 Feature Selection
  • 10.2 Validation
    • 10.3.1 Nearest Neighbor
    • 10.3.2 Nearest Centroid
    • 10.3.3 Neural Networks
    • 10.3.4 Support Vector Machine
  • 10.4 Performance Evaluation
  • 10.5 Example I: Classification of Bladder Cancer Subtypes
  • 10.6 Example II: Classification of SRBCT Cancer Subtypes
  • 10.7 Summary
  • 10.8 Further Reading
• 11. The Design of Probes for Arrays
  • 11.1 Selection of Genes for an Array
  • 11.2 Gene Finding
  • 11.3 Selection of Regions Within Genes
  • 11.4 Selection of Primers for PCR
    • 11.4.1 Example: Finding PCR Primers for Gene AF105374
  • 11.5 Selection of Unique Oligomer Probes
  • 11.6 Remapping of Probes
  • 11.7 Further Reading
• 12. Genotyping and Resequencing Chips
  • 12.1 Example: Neural Networks for GeneChip Prediction
  • 12.2 Further Reading
• 13. Experiment Design and Interpretation of Results
  • 13.1 Factorial Designs
  • 13.2 Designs for Two-Channel Arrays
  • 13.3 Hypothesis Driven Experiments
  • 13.4 Independent Verification
  • 13.5 Interpretation of Results
  • 13.6 Limitations of Expression Analysis
    • 13.6.1 Relative Versus Absolute RNA Quantification
  • 13.7 Further Reading
• 14. Software Issues and Data Formats
  • 14.1 Standardization Efforts
  • 14.2 Databases
  • 14.3 Standard File Format
  • 14.4 Software for Clustering
    • 14.4.1 Example: Clustering with ClustArray
  • 14.5 Software for Statistical Analysis
    • 14.5.1 Example: Statistical Analysis with R
    • 14.5.2 The Affy Package of Bioconductor
    • 14.5.3 Commercial Statistics Packages
  • 14.6 Summary
  • 14.7 Further Reading
• Appendix A: Web Resources: Commercial Software Packages
• References
• Index

Keywords

vector angle distance, patient axes, variance between replicates, positive regulatory effect, gene expression data, negative regulatory effect, microarray data, spotted array, probe pairs, gene finding, fold change, reference pool, functional annotation, microarray experiments, nonlinear data, four genes, genetic network, patient category, expression array, six replicates, interaction matrix, first principal component, regulatory networks, function prediction, distance matrix