Synthesizes the Vast Literature on One of the Hottest Areas in Biomedical ResearchBuilding a bridge between pharmacogenomics and statistics, Statistical and Computational Pharmacogenomicsallows researchers to readily familiarize themselves with this promising and revolutionary area of science. It outlines the powerful statistical techniques used in the fast-growing field of pharmacogenomics, which seeks to understand the relationships between interpatient variability in drug response and specific genomic sites. Providing geneticists with the tools needed to understand and model the genetic variations for drug responses, this seminal work also equips statisticians with the motivation and ideas needed to explore genomic data.Exciting Implications for the Future of Drug TherapiesIn addition to providing a synthesis of statistical methodology for the pharmocogenomic study of drug response, this cutting-edge, authoritative text developseach method step-by-step, while keeping theoretical details to a minimum. It also presents detailed, worked examples that outline how to apply the discussed methods and outlines the necessary statistical and computational theories for genetic mapping of dynamic traits.Indicative of the depth of this groundbreaking, multidisciplinary research and its exciting implications for the future of drug therapies, it is now possible to document, map, and understand the structure and patterns of the human genome linked to drug response. The pioneering process of functional mapping has the potential to revolutionize the use of many medications with tailored treatment plansbased on patients' individual genetic makeup. This will ideally lead to optimal prescriptions, optimal administration times, and optimal dosage scheduling.
... a statistically rigorous text that gives a systematic exposition of the subject of pharmacogenomics, the related analytical methods and the corresponding computational algorithms. ... a good basis for further methodological, empirical and applied investigation into the field. -Statistics in Medicine, 2011, 30 This text is one of the first books written by statisticians and for statisticians who need to know the basics of genetic markers based on genomic mapping and haplotyping. ... this book is a welcome addition that will help me learn pharmacogenomics to the extent that I need it to apply appropriate statistical methodology in microarray analysis and classification problems. ... I can recommend it for the statisticians ... . I also hope that it will be successful at getting the chemists, biologists, and geneticists interested in the important statistical methods and mathematical modeling described in this book. -Michael R. Chernick, Technometrics, February 2011 This book covers advanced topics in statistical genetics focusing on applications of interest in pharmacogenomics. The difficulties in estimating haplotype frequencies and their effects on quantitative trait loci (QTLs) are covered in detail for a variety of experimental designs. ... of most interest for statisticians working in the pharmaceutical area that need to incorporate genetic variables into consideration in their studies. -ISCB News, No. 50, December 2010 ... [Pharmacogenomics] can address questions such as whether individuals with different versions of a gene are more or less likely to respond to a particular drug. However, Wu and Lin go well beyond this and discuss methods for relating genetic variation to dynamic pharmacokinetic and pharmacodynamic profiles of drugs. They refer to this as 'functional mapping'. ... One of the main clinical applications of these methods will be in predicting efficacy and toxicity of drugs, allowing treatment to be tailored to an individual's genetic background, and this book makes a valuable contribution towards this. -Significance, June 2010 ...a volume that can be recommended to both statisticians and life scientists. Yes, there's plenty of heavy-duty math for the theory lovers, but there are also many sections of explanations for the biologist. These explanations are not highly theoretical and give the scientist a better understanding of what the analysis is doing and why it is needed. -John A. Wass, Ph.D., Scientific Computing, 2009
| Designs and Strategies for Genomic Mapping and Haplotyping | p. 1 |
| Fundamental Genetics | p. 1 |
| Chromosomes and Map | p. 1 |
| Genotype and Phenotype | p. 2 |
| Molecular Genetic Markers | p. 3 |
| The HapMap | p. 4 |
| Pharmacogenetics and Pharmacogenomics | p. 5 |
| Genetic Designs | p. 8 |
| Experimental Crosses | p. 8 |
| Nuclear Families | p. 9 |
| Natural Populations with Unrelated Individuals | p. 9 |
| Natural Populations with Unrelated Families | p. 10 |
| Strategies for Genomic Mapping | p. 11 |
| Linkage Mapping | p. 11 |
| Linkage Disequilibrium Mapping | p. 13 |
| Joint Linkage and Linkage Disequilibrium Mapping | p. 15 |
| From QTL to QTN | p. 16 |
| Genotype and Diplotype | p. 17 |
| Identification of QTNs | p. 18 |
| Functional Mapping of Drug Response | p. 19 |
| Genetic Haplotyping in Natural Populations | p. 21 |
| Notation and Definitions | p. 21 |
| Likelihoods | p. 23 |
| The EM Algorithm | p. 24 |
| Sampling Variances of Parameter Estimates | p. 25 |
| Model Selection | p. 27 |
| Hypothesis Tests | p. 28 |
| Haplotyping with Multiple SNPs | p. 29 |
| Haplotype Structure | p. 29 |
| Likelihoods and Algorithms | p. 31 |
| R-SNP Model | p. 35 |
| Genetic Haplotyping in Experimental Crosses | p. 39 |
| LD Analysis in the F[subscript 1]'s Gamete Population | p. 40 |
| A General Model | p. 40 |
| A Special Case: Two-Point LD | p. 41 |
| A Special Case: Three-Point LD | p. 41 |
| LD Analysis in the Backcross | p. 43 |
| Design | p. 43 |
| Analysis of Variance | p. 44 |
| t-Test | p. 44 |
| LD Analysis in the F[subscript 2] | p. 47 |
| Mixture Model | p. 47 |
| Likelihoods, Estimation, and Hypothesis Tests | p. 48 |
| Model Selection: Two- vs. Three-Point LD Analysis | p. 48 |
| LD Analysis in a Full-Sib Family | p. 51 |
| Introduction | p. 51 |
| A General Model | p. 52 |
| Estimation | p. 53 |
| Multiple Segregating Types of Markers | p. 56 |
| Three-Point Haplotyping | p. 57 |
| Prospects | p. 58 |
| A General Quantitative Model for Genetic Haplotyping | p. 61 |
| Quantitative Genetic Models | p. 62 |
| Population Structure | p. 62 |
| Biallelic Model | p. 62 |
| Triallelic Model | p. 63 |
| Quadriallelic Model | p. 64 |
| Likelihood | p. 65 |
| The EM Algorithm | p. 67 |
| Model Selection | p. 67 |
| Hypothesis Tests | p. 67 |
| Three-SNP Haplotyping | p. 68 |
| Haplotyping in a Non-Equilibrium Population | p. 70 |
| Prospects | p. 73 |
| Basic Principle of Functional Mapping | p. 75 |
| Dynamic Genetic Control | p. 76 |
| Structure of Functional Mapping | p. 77 |
| Mixture Model | p. 78 |
| Modeling the Mean-Covariance Structure | p. 79 |
| Estimation of Functional Mapping | p. 82 |
| Likelihood | p. 82 |
| Algorithm | p. 83 |
| Hypothesis Tests of Functional Mapping | p. 84 |
| Transform-Both-Sides Model of Functional Mapping | p. 88 |
| Structured Antedependence Model of Functional Mapping | p. 90 |
| Antedependence Model | p. 90 |
| Structured Antedependence Model | p. 90 |
| Model Selection | p. 91 |
| An Optimal Strategy of Structuring the Covariance | p. 91 |
| Standard Deviation Function | p. 92 |
| Correlation Function | p. 92 |
| Model Selection | p. 93 |
| Functional Mapping Meets Ontology | p. 94 |
| Functional Mapping of Pharmacokinetics and Pharmacodynamics | p. 97 |
| Mathematical Modeling of Pharmacokinetics and Pharmacodynamics | p. 98 |
| Modeling Pharmacokinetics | p. 98 |
| Modeling Pharmacodynamics | p. 98 |
| Linking Pharmacokinetics and Pharmacodynamics | p. 100 |
| Functional Mapping of Pharmacokinetics | p. 101 |
| Kinetic Derivation of a Bi-Exponential Model | p. 102 |
| QTL Mapping with a Bi-Exponential Model | p. 104 |
| Functional Mapping Based on Ho et al.'s Kinetic Model | p. 112 |
| Functional Mapping of Pharmacodynamics | p. 114 |
| Patterns of Genetic Control in Pharmacodynamics | p. 114 |
| Sequencing Pharmacodynamics | p. 115 |
| Basic Model | p. 115 |
| A Pharmacogenetic Study of Heart Rate Responses | p. 117 |
| Haplotyping Drug Response by Linking Pharmacokinetics and Pharmacodynamics | p. 123 |
| A Unifying Model for Functional Mapping | p. 123 |
| Clinical Design | p. 123 |
| Likelihood | p. 124 |
| Modeling the Mean Vector | p. 128 |
| Modeling the Covariance Structure | p. 128 |
| Algorithms and Determination of Risk Haplotypes | p. 133 |
| Hypothesis Tests | p. 133 |
| Computer Simulation | p. 135 |
| Genetic and Statistical Considerations | p. 138 |
| Functional Mapping of Biological Clocks | p. 141 |
| Mathematical Modeling of Circadian Rhythms | p. 142 |
| Haplotyping Circadian Rhythms | p. 143 |
| Study Design | p. 143 |
| Antedependence Model | p. 144 |
| Likelihood | p. 146 |
| Algorithm and Determination of Risk Haplotypes | p. 147 |
| Hypothesis Testing | p. 148 |
| Existence of Risk Haplotypes | p. 148 |
| Pleiotropic Effect on mRNA or Protein Rhythms | p. 149 |
| Risk Haplotypes for the Behavior and Shape of Circadian Rhythms | p. 149 |
| Simulation | p. 150 |
| Fourier Series Approximation of Circadian Rhythms | p. 150 |
| Introduction | p. 150 |
| Fourier Model | p. 151 |
| Genetic Haplotyping | p. 153 |
| Further Considerations | p. 156 |
| Genetic Mapping of Allometric Scaling | p. 159 |
| Allometric Models | p. 159 |
| Allometric Mapping | p. 161 |
| Genetic Design | p. 161 |
| Likelihood and Estimation | p. 162 |
| Hypothesis Testing | p. 164 |
| Allometric Mapping with a Pleiotropic Model | p. 165 |
| Design | p. 165 |
| Genetic Model | p. 165 |
| Statistical Estimation | p. 167 |
| Hypothesis Tests | p. 167 |
| Allometric Mapping with General Power Equations | p. 168 |
| Estimating Power Coefficients Using Model II Non-Linear Regression | p. 168 |
| Predicting Dependent Variables | p. 170 |
| Functional Mapping of Drug Response with Allometric Scaling | p. 175 |
| Allometric Scaling of Pharmacokinetic and Pharmacodynamic Responses | p. 176 |
| Model Derivations | p. 177 |
| Experimental Design | p. 177 |
| Model Structure and Estimation | p. 178 |
| Hypothesis Testing | p. 179 |
| A Pleiotropic Model for Allometric Mapping | p. 184 |
| Genetic Haplotyping with Developmental Allometry | p. 184 |
| Likelihood | p. 185 |
| Algorithm | p. 187 |
| Hypothesis Testing | p. 189 |
| Joint Functional Mapping of Drug Efficacy and Toxicity | p. 195 |
| A Joint Model | p. 196 |
| Genetic Design | p. 196 |
| Clinical Design | p. 197 |
| Statistical Design | p. 198 |
| The Haplotyping Framework | p. 198 |
| Covariance Structure | p. 201 |
| Algorithm and Determination of Risk Haplotypes | p. 203 |
| Hypothesis Testing | p. 203 |
| Existence of Risk Haplotypes | p. 204 |
| Different Risk Haplotypes for PK and PD | p. 204 |
| Different Risk Haplotypes for Drug Efficacy and Drug Toxicity | p. 205 |
| Risk Haplotypes Responsible for Individual Curve Parameters | p. 206 |
| Closed Forms for the SAD Structure | p. 210 |
| Allometric Mapping of Drug Efficacy and Drug Toxicity | p. 211 |
| Modeling Epistatic Interactions in Drug Response | p. 213 |
| Quantitative Genetic Models for Epistasis | p. 214 |
| Definition and Type | p. 214 |
| Quantifying Epistasis | p. 215 |
| From Static to Dynamic | p. 216 |
| Haplotyping Epistasis | p. 217 |
| Population Genetic Structure | p. 217 |
| Genetic Design | p. 218 |
| Population Genetic Model | p. 219 |
| Likelihood for Estimating Across-Block Haplotype Frequencies | p. 219 |
| Likelihood for Haplotype-Haplotype Interaction Effects | p. 226 |
| Hypothesis Tests | p. 228 |
| Haplotyping Epistasis of Drug Response | p. 233 |
| Introduction | p. 233 |
| Model and Estimation | p. 233 |
| Hypothesis Tests | p. 235 |
| Prospects | p. 243 |
| Mapping Genotype-Environment Interactions in Drug Response | p. 245 |
| Haplotyping Genotype-Environment Interactions | p. 246 |
| Environmental Sensitivity and Genotype-Environment Interactions | p. 246 |
| Genetic Design | p. 248 |
| Likelihoods | p. 249 |
| The EM Algorithm | p. 252 |
| Model Selection | p. 252 |
| Hypothesis Tests | p. 252 |
| Haplotyping with Multiple SNPs | p. 255 |
| Haplotyping Genotype-Environment Interactions for Pharmacological Processes | p. 259 |
| Introduction | p. 259 |
| Dynamic Model | p. 261 |
| Hypothesis Testing | p. 262 |
| Genetic Considerations | p. 268 |
| Nonparametric Functional Mapping of Drug Response | p. 271 |
| Nonparametric Modeling with Legendre Polynomial | p. 272 |
| Legendre Orthogonal Polynomials | p. 272 |
| Genetic Design | p. 273 |
| Likelihoods | p. 275 |
| Model Selection | p. 276 |
| Hypothesis Tests | p. 277 |
| Nonparametric Modeling of Event Processes with Legendre Polynomial | p. 278 |
| Introduction | p. 278 |
| Model and Estimation | p. 278 |
| Hypothesis Testing | p. 280 |
| Nonparametric Functional Mapping with B-Spline | p. 282 |
| Basics of B-Splines | p. 282 |
| Haplotyping Model for DNA Sequence Variants | p. 285 |
| Nonparametric Functional Mapping of Pharmacokinetics and Pharmacodynamics | p. 285 |
| Nonparametric Modeling of the Covariance Structure | p. 286 |
| Semiparametric Functional Mapping of Drug Response | p. 287 |
| Problems | p. 288 |
| Long-Term HIV Dynamics | p. 288 |
| Different Phases of Programmed Cell Death | p. 290 |
| Semiparametric Modeling of Functional Mapping: HIV Dynamics | p. 291 |
| Genetic Design | p. 291 |
| Model Structure | p. 292 |
| Model Estimation | p. 296 |
| Hypothesis Testing | p. 297 |
| Semiparametric Modeling of Functional Mapping: PCD | p. 299 |
| Phase Dissection of Growth | p. 299 |
| Haplotyping Model | p. 302 |
| Computation Algorithms | p. 303 |
| Hypothesis Testing | p. 304 |
| References | p. 309 |
| Author Index | p. 333 |
| Subject Index | p. 341 |
| Table of Contents provided by Ingram. All Rights Reserved. |
ISBN: 9781584888284
ISBN-10: 1584888288
Series: Chapman & Hall/CRC Interdisciplinary Statistics Series
Audience:
Professional
Format:
Hardcover
Language:
English
Number Of Pages: 368
Published: 1st July 2008
Dimensions (cm): 23.5 x 15.6
x 2.2
Weight (kg): 0.658