Cancer diagnostics with DNA microarrays

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Datensatz im Suchindex

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adam_text Contents Preface xv Acknowledgments xvii 1. Introduction to DNA Microarray Technology 1 1.1 Hybridization / 1 1.2 The Technology Behind DNA Microarrays / 3 1.2.1 Affymetrix GeneChip Technology / 4 1.2.2 Spotted Arrays / 6 1.2.3 Digital Micromirror Arrays / 8 1.2.4 InkJet Arrays / 8 1.2.5 Bead Arrays / 9 1.2.6 Electronic Microarrays / 9 1.2.7 Serial Analysis of Gene Expression (SAGE) / 10 1.3 Parallel Sequencing on Microbead Arrays / II 1.3.1 Emerging Technologies / 12 1.4 Summary / 13 Further Reading / 14 2. Image Analysis 16 2.1 Gridding / 16 2.2 Segmentation / 17 2.3 Intensity Extraction / 17 2.4 Background Correction / 17 Viii CONTENTS 2.5 Software / 19 2.5.1 Free Software for Array Image Analysis / 19 2.5.2 Commercial Software for Array Image Analysis / 19 2.6 Summary / 20 3. Basic Data Analysis 22 3.1 Normalization / 22 3.1.1 One or More Genes Assumed Expressed at Constant Rate / 23 3.1.2 Sum of Genes Is Assumed Constant / 24 3.1.3 Subset of Genes Is Assumed Constant / 24 3.1.4 Majority of Genes Assumed Constant / 24 3.1.5 Logit Normalization / 24 3.1.6 Spike Controls / 25 3.2 Dye Bias, Spatial Bias, Print Tip Bias / 25 3.3 Expression Indices / 26 3.3.1 Average Difference / 26 3.3.2 Signal / 26 3.3.3 Model Based Expression Index / 26 3.3.4 Robust Multiarray Average / 27 3.3.5 Position Dependent Nearest Neighbor Model / 27 3.3.6 Logit t / 27 3.4 Detection of Outliers / 28 3.5 Fold Change / 28 3.6 Significance / 29 3.6.1 Multiple Conditions / 30 3.6.2 Nonparametric Tests / 30 3.6.3 Correction for Multiple Testing / 30 3.6.4 Example I: f Test and ANOVA / 31 3.6.5 Example II: Number of Replicates / 32 3.7 Mixed Cell Populations / 33 3.8 Summary / 34 Further Reading / 34 4. Visualization by Reduction of Dimensionality 37 4.1 Principal Component Analysis / 37 4.2 Supervised Principal Component Analysis / 39 4.3 Independent Component Analysis / 39 4.4 Example I: PCA on Small Data Matrix / 39 4.5 Example II: PCA on Real Data / 41 4.6 Summary / 42 Further Reading / 42 5. Cluster Analysis 44 5.1 Hierarchical Clustering / 44 CONTENTS IX 5.2 A Means Clustering / 46 5.3 Self Organizing Maps / 46 5.4 Distance Measures / 47 5.4.1 Example: Comparison of Distance Measures / 49 5.5 Time Series Analysis / 51 5.6 Gene Normalization / 51 5.7 Visualization of Clusters / 52 5.8 Summary / 52 Further Reading / 52 6. Molecular Classifiers for Cancer 54 6.1 Supervised versus Unsupervised Analysis / 54 6.2 Feature Selection / 55 6.3 Validation / 55 6.4 Classification Schemes / 56 6.4.1 Nearest Neighbor / 56 6.4.2 Nearest Centroid / 57 6.4.3 Neural Networks / 57 6.4.4 Support Vector Machine / 58 6.5 Performance Evaluation / 58 6.6 Example I: Classification of SRBCT Cancer Subtypes / 59 6.7 A Network Approach to Molecular Classification / 59 6.7.1 Construction of HG U95Av2 Chip Based Gene Network / 61 6.7.2 Construction of HG U133A Chip Based Gene Network / 61 6.7.3 Example: Lung Cancer Classification with Mapped Subnetwork / 61 6.7.4 Example: Brain Cancer Classification with Mapped Subnetwork / 62 6.7.5 Example: Breast Cancer Classification with Mapped Subnetwork / 62 6.7.6 Example: Leukemia Classification with Mapped Subnetwork / 62 6.8 Summary / 63 Further Reading / 64 7. Survival Analysis 66 7.1 Kaplan Meier Approach / 66 7.2 Cox Proportional Hazards Model / 67 7.3 Software / 68 Further Reading / 68 8. Meta Analysis 69 8.1 Gene Matching / 69 8.2 Combining Measurements / 70 8.2.1 Intensity / 70 X CONTENTS 8.2.2 Effect Size / 70 8.2.3 P Values / 70 8.2.4 Selected Features / 70 8.2.5 Vote Counting / 70 8.3 Meta Classification / 71 8.4 Summary / 71 Further Reading / 71 9. The Design of Probes for Arrays 73 9.1 Gene Finding / 73 9.2 Selection of Regions Within Genes / 74 9.3 Selection of Primers for PCR / 74 9.3.1 Example: Finding PCR Primers for Gene AF105374 / 74 9.4 Selection of Unique Oligomer Probes / 75 9.5 Remapping of Probes / 76 Further Reading / 76 10. Software Issues and Data Formats 78 10.1 Standardization Efforts / 79 10.2 Databases / 79 10.3 Standard File Format / 79 10.4 Software for Clustering / 80 10.5 Software for Statistical Analysis / 80 10.5.1 Example: Statistical Analysis with R / 80 10.5.2 The affy Package of Bioconductor / 83 10.5.3 Survival Analysis / 85 10.5.4 Commercial Statistics Packages / 85 10.6 Summary / 85 Further Reading / 85 11. Breast Cancer 87 11.1 Introduction / 87 11.1.1 Anatomy of the Breast / 87 11.1.2 Breast Tumors / 87 11.2 Current Diagnosis / 88 11.2.1 Staging / 88 11.2.2 Histopathological Grading / 89 11.2.3 Clinical Markers / 89 11.3 Current Therapy / 90 11.3.1 Surgery / 90 11.3.2 Chemotherapy / 90 11.3.3 Hormone Therapy / 90 11.3.4 Monoclonal Antibody Therapy / 90 CONTENTS XI 11.4 Microarray Studies of Breast Cancer / 90 11.4.1 The Stanford Group / 90 11.4.2 The Netherlands Cancer Institute Group / 91 11.4.3 The Duke University Group / 92 11.4.4 The Lund Group / 92 11.4.5 The Karolinska Group / 93 11.4.6 The Tokyo Group / 93 11.4.7 The Veridex Group / 93 11.4.8 The National Cancer Institute Group / 93 11.5 Meta Classification of Breast Cancer / 93 11.6 Summary / 95 Further Reading / 95 12. Leukemia 97 12.1 Current Diagnosis / 98 12.2 Current Therapy / 98 12.3 Microarray Studies of Leukemia / 99 12.3.1 The Boston Group / 99 12.3.2 The Austria Group / 99 12.3.3 The Utah Group / 99 12.3.4 The Memphis Group / 100 12.3.5 The Japan Group / 100 12.3.6 The Munich Group / 100 12.3.7 The Stanford Group / 101 12.3.8 The Copenhagen Group / 101 12.3.9 The Netherlands Group / 101 12.4 Summary / 101 Further Reading / 101 13. Lymphoma 104 13.1 Microarray Studies of Lymphoma / 105 13.1.1 The Stanford Group / 105 13.1.2 The Boston Group / 105 13.1.3 The NIH Group / 105 13.1.4 The NCI Group / 106 13.2 Meta Classification of Lymphoma / 106 13.2.1 Matching of Components / 107 13.2.2 Blind Test Set / 109 13.3 Summary / 112 Further Reading / 112 14. Lung Cancer 114 14.1 Microarray Studies of Lung Cancer / 114 14.1.1 The Harvard/Whitehead Group / 114 XH CONTENTS 14.1.2 The Minnesota Group / 116 14.1.3 The Vanderbilt Group / 116 14.1.4 The Tokyo Group / 116 14.1.5 The Michigan Group / 116 14.1.6 The Mayo Clinic / 116 14.1.7 The Toronto Group / 117 14.1.8 The NIH Group / 117 14.1.9 The Stanford Group / 117 14.1.10 The Israel Group / 117 14.2 Meta Classification of Lung Cancer / 117 14.3 Summary / 122 Further Reading / 122 15. Bladder Cancer 123 15.1 Microarray Studies of Bladder Cancer / 124 15.1.1 The Aarhus Group / 124 15.1.2 The New York Group / 125 15.1.3 The Dusseldorf Group / 125 15.2 Summary / 125 Further Reading / 125 16. Colon Cancer 127 16.1 Microarray Studies of Colon Cancer / 127 16.1.1 The Princeton Group / 127 16.1.2 The Maryland Group / 128 16.1.3 The Aarhus Group / 128 16.1.4 The Marseilles Group / 128 16.1.5 The San Diego Group / 128 16.1.6 The Helsinki Group / 129 16.2 Summary / 129 Further Reading / 129 17. Ovarian Cancer 130 17.1 Microarray Studies of Ovarian Cancer / 130 17.1.1 Duke University Medical Center / 130 17.1.2 The Stanford Group / 131 17.1.3 The London Group / 131 17.1.4 The UCLA Group / 131 17.1.5 The NIH Group / 131 17.1.6 The Novartis Group / 132 17.2 Summary / 132 Further Reading / 132 CONTENTS Xlii 18. Prostate Cancer 134 18.1 Microarray Studies of Prostate Cancer / 134 18.1.1 University of Michigan Medical School / 134 18.1.2 Memorial Sloan Kettering Cancer Center / 134 18.1.3 The NIH Group / 135 18.1.4 The Harvard Group / 135 18.1.5 The Australian Group / 135 18.1.6 The Stanford Group / 136 18.2 Summary / 136 Further Reading / 136 19. Melanoma 138 19.1 Microarray Studies of Melanoma / 138 19.1.1 Memorial Sloan Kettering Cancer Center / 138 19.1.2 The NIH Group / 138 19.2 Summary / 139 Further Reading / 139 20. Brain Tumors 142 20.1 Microarray Studies of Brain Tumors / 144 20.1.1 Harvard Medical School / 144 20.1.2 M. D. Anderson Cancer Center / 144 20.1.3 UCLA School of Medicine / 144 20.1.4 The Lausanne Group / 144 20.1.5 Deutsches Krebsforschungszentrum / 144 20.1.6 Children s Hospital, Boston / 145 20.2 Summary / 145 Further Reading / 145 21. Organ or Tissue Specific Classification 147 Further Reading / 148 22. Sample Collection and Stability 149 22.1 Tissue Samples / 149 22.1.1 Stability of Tissue After Surgical Removal / 149 22.1.2 Stability of Sample in Storage / 150 22.1.3 Paraffin Embedded Tissue Samples / 150 22.2 Blood Samples / 150 22.3 Sample Heterogeneity / 151 XIV CONTENTS 22.4 Summary / 151 Further Reading / 151 References 152 Index 183
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spellingShingle Cancer diagnostics with DNA microarrays
DNA microarrays Diagnostic use
Cancer Diagnosis
Neoplasms diagnosis
Oligonucleotide Array Sequence Analysis methods
Data Interpretation, Statistical
DNS-Chip (DE-588)4721796-0 gnd
Krebs Medizin (DE-588)4073781-0 gnd
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title Cancer diagnostics with DNA microarrays
title_auth Cancer diagnostics with DNA microarrays
title_exact_search Cancer diagnostics with DNA microarrays
title_full Cancer diagnostics with DNA microarrays Steen Knudsen
title_fullStr Cancer diagnostics with DNA microarrays Steen Knudsen
title_full_unstemmed Cancer diagnostics with DNA microarrays Steen Knudsen
title_short Cancer diagnostics with DNA microarrays
title_sort cancer diagnostics with dna microarrays
topic DNA microarrays Diagnostic use
Cancer Diagnosis
Neoplasms diagnosis
Oligonucleotide Array Sequence Analysis methods
Data Interpretation, Statistical
DNS-Chip (DE-588)4721796-0 gnd
Krebs Medizin (DE-588)4073781-0 gnd
Diagnostik (DE-588)4113303-1 gnd
topic_facet DNA microarrays Diagnostic use
Cancer Diagnosis
Neoplasms diagnosis
Oligonucleotide Array Sequence Analysis methods
Data Interpretation, Statistical
DNS-Chip
Krebs Medizin
Diagnostik
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