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A Statistical Approach to Genetic Epidemiology


A Statistical Approach to Genetic Epidemiology

Concepts and Applications, with an e-Learning Platform
4. Aufl.

von: Andreas Ziegler, Inke R. Kônig, Friedrich Pahlke

76,99 €

Verlag: Wiley-Blackwell
Format: EPUB
Veröffentl.: 24.08.2011
ISBN/EAN: 9783527633661
Sprache: englisch
Anzahl Seiten: 522

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Beschreibungen

<b>A Statistical Approach to Genetic Epidemiology</b> <p>After studying statistics and mathematics at the University of Munich and obtaining his doctoral degree from the University of Dortmund, <b>Andreas Ziegler</b> received the Johann-Peter-Süssmilch-Medal of the German Association for Medical Informatics, Biometry and Epidemiology for his post-doctoral work on “Model Free Linkage Analysis of Quantitative Traits” in 1999. In 2004, he was one of the recipients of the Fritz-Linder-Forum-Award from the German Association for Surgery.
<p>Foreword to the First Edition vii</p> <p>Foreword to the Second Edition viii</p> <p>Preface xi</p> <p>Acknowledgments xv</p> <p><b>1 Molecular Genetics 1</b></p> <p>1.1 Genetic information 2</p> <p>1.1.1 Location of genetic information 2</p> <p>1.1.2 Interpretation of genetic information 5</p> <p>1.1.3 Translation of genetic information 5</p> <p>1.2 Transmission of genetic information 7</p> <p>1.3 Variations in genetic information 10</p> <p>1.3.1 Individual differences in genetic information 10</p> <p>1.3.2 Detection of variations 12</p> <p>1.3.3 Probability for detection of variations 16</p> <p>1.4 Problems 18</p> <p><b>2 Formal Genetics 21</b></p> <p>2.1 Mendel and his laws 22</p> <p>2.2 Segregation patterns 23</p> <p>2.2.1 Autosomal dominant inheritance 24</p> <p>2.2.2 Autosomal recessive inheritance 25</p> <p>2.2.3 X-chromosomal dominant inheritance 26</p> <p>2.2.4 X-chromosomal recessive inheritance 27</p> <p>2.2.5 Y-chromosomal inheritance 28</p> <p>2.3 Complications of Mendelian segregation 28</p> <p>2.3.1 Variable penetrance and expression 29</p> <p>2.3.2 Age-dependent penetrance 31</p> <p>2.3.3 Imprinting 33</p> <p>2.3.4 Phenotypic and genotypic heterogeneity 35</p> <p>2.3.5 Complex diseases 36</p> <p>2.4 Hardy–Weinberg law 38</p> <p>2.5 Problems 43</p> <p><b>3 Genetic Markers 47</b></p> <p>3.1 Properties of genetic markers 47</p> <p>3.2 Types of genetic markers 52</p> <p>3.2.1 Short tandem repeats (STRs) 52</p> <p>3.2.2 Single nucleotide polymorphisms (SNPs) 54</p> <p>3.3 Genotyping methods for SNPs 57</p> <p>3.3.1 Restriction fragment length polymorphism analysis 58</p> <p>3.3.2 Real-time polymerase chain reaction 58</p> <p>3.3.3 Matrix assisted laser desorption/ionization time of flight genotyping 61</p> <p>3.3.4 Chip-based genotyping 61</p> <p>3.3.5 Choice of genotyping method 63</p> <p>3.4 Problems 65</p> <p><b>4 Data Quality 67</b></p> <p>4.1 Pedigree errors 68</p> <p>4.2 Genotyping errors in pedigrees 70</p> <p>4.2.1 Frequency of genotyping errors 70</p> <p>4.2.2 Reasons for genotyping errors 71</p> <p>4.2.3 Mendel checks 72</p> <p>4.2.4 Checks for double recombinants 74</p> <p>4.3 Genotyping errors and Hardy–Weinberg equilibrium (HWE) 76</p> <p>4.3.1 Causes of deviations from HWE 77</p> <p>4.3.2 Tests for deviation from HWE for SNPs 78</p> <p>4.3.3 Tests for deviation from HWE for STRs 81</p> <p>4.3.4 Measures for deviation from HWE 83</p> <p>4.3.5 Tests for compatibility with HWE for SNPs 86</p> <p>4.4 Quality control in high-throughput studies 91</p> <p>4.4.1 Sample quality control 94</p> <p>4.4.2 SNP quality control 97</p> <p>4.5 Cluster plot checks and internal validity 98</p> <p>4.5.1 Cluster compactness measures 101</p> <p>4.5.2 Cluster connectedness measures 101</p> <p>4.5.3 Cluster separation measures 101</p> <p>4.5.4 Genotype stability measures 102</p> <p>4.5.5 Combinations of criteria 102</p> <p>4.6 Problems 109</p> <p><b>5 Genetic Map Distances 113</b></p> <p>5.1 Physical distance 113</p> <p>5.2 Map distance 114</p> <p>5.2.1 Distance 114</p> <p>5.2.2 Specific map functions 115</p> <p>5.2.3 Correspondence between physical distance and map distance 116</p> <p>5.2.4 Multilocus feasibility 117</p> <p>5.3 Linkage disequilibrium distance 118</p> <p>5.4 Problems 123</p> <p><b>6 Family Studies 125</b></p> <p>6.1 Family history method and family study method 127</p> <p>6.2 Familial correlations and recurrence risks 129</p> <p>6.2.1 Familial resemblance 129</p> <p>6.2.2 Recurrence risk ratios 131</p> <p>6.3 Heritability 134</p> <p>6.3.1 The simple Falconer model 135</p> <p>6.3.2 The general Falconer model 137</p> <p>6.3.3 Kinship coefficient and Jacquard’s Δ7 coefficient 138</p> <p>6.4 Twin and adoption studies 141</p> <p>6.4.1 Twin studies 141</p> <p>6.4.2 Adoption studies 142</p> <p>6.5 Critique on investigating familial resemblance 143</p> <p>6.6 Segregation analysis 144</p> <p>6.7 Problems 154</p> <p><b>7 Model-Based Linkage Analysis 155</b></p> <p>7.1 Linkage analysis between two genetic markers 156</p> <p>7.1.1 Linkage analysis in phase-known pedigrees 156</p> <p>7.1.2 Linkage analysis in phase-unknown pedigrees 160</p> <p>7.1.3 Linkage analysis in pedigrees with missing genotypes 161</p> <p>7.2 Linkage analysis between a genetic marker and a disease 167</p> <p>7.2.1 Linkage analysis between a genetic marker and a disease in phase-known pedigrees 168</p> <p>7.2.2 Linkage analysis between a genetic marker and a disease in general cases 172</p> <p>7.2.3 Gain in information by genotyping additional individuals; power calculations 177</p> <p>7.3 Significance levels in linkage analysis 180</p> <p>7.4 Problems 184</p> <p><b>8 Model-Free Linkage Analysis 189</b></p> <p>8.1 The principle of similarity 190</p> <p>8.2 Mathematical foundation of affected sib-pair analysis 192</p> <p>8.3 Common tests for affected sib-pair analysis 193</p> <p>8.3.1 The maximum LOD score and the triangle test 194</p> <p>8.3.2 Score- and Wald–type 1 degree of freedom tests 201</p> <p>8.3.3 Affected sib-pair tests using alleles shared identical by state 206</p> <p>8.4 Properties of affected sib-pair tests 206</p> <p>8.5 Sample size and power calculations for affected sib-pair studies 207</p> <p>8.5.1 Functional relation between identical by descent probabilities and recurrence risk ratios 207</p> <p>8.5.2 Sample size and power calculations for the mean test using recurrence risk ratios 209</p> <p>8.6 Extensions to multiple marker loci 212</p> <p>8.7 Extension to large sibships 213</p> <p>8.8 Extension to large pedigrees 214</p> <p>8.9 Extensions of the affected sib-pair approach 216</p> <p>8.9.1 Covariates in affected sib-pair analyses 216</p> <p>8.9.2 Multiple disease loci in affected sib-pair analyses 216</p> <p>8.9.3 Estimating the position of the disease locus in affected sib-pair analyses 217</p> <p>8.9.4 Typing unaffected relatives in sib-pair analyses 217</p> <p>8.10 Problems 218</p> <p><b>9 Quantitative Traits 221</b></p> <p>9.1 Quantitative versus qualitative traits 222</p> <p>9.2 The Haseman–Elston method 223</p> <p>9.2.1 The expected squared phenotypic difference at the trait locus 225</p> <p>9.2.2 The expected squared phenotypic difference at the marker locus 227</p> <p>9.3 Extensions of the Haseman–Elston method 229</p> <p>9.3.1 Double squared trait difference 230</p> <p>9.3.2 Extension to large sibships 230</p> <p>9.3.3 Haseman–Elston revisited and the new Haseman–Elston method 231</p> <p>9.3.4 Power and sample size calculations 234</p> <p>9.4 Variance components models 237</p> <p>9.4.1 The univariate variance components model 237</p> <p>9.4.2 The multivariate variance components model 238</p> <p>9.5 Random sib-pairs, extreme probands and extreme sib-pairs 240</p> <p>9.6 Empirical determination of p-values 243</p> <p>9.7 Problems 245</p> <p><b>10 Fundamental Concepts of Association Analyses 247</b></p> <p>10.1 Introduction to association 247</p> <p>10.1.1 Principles of association 247</p> <p>10.1.2 Study designs for association 249</p> <p>10.2 Linkage disequilibrium 250</p> <p>10.2.1 Allelic linkage disequilibrium 250</p> <p>10.2.2 Genotypic linkage disequilibrium 255</p> <p>10.2.3 Extent of linkage disequilibrium 259</p> <p>10.3 Problems 262</p> <p><b>11 Association Analysis in Unrelated Individuals 265</b></p> <p>11.1 Selection of cases and controls 266</p> <p>11.2 Tests, estimates, and a comparison 266</p> <p>11.2.1 Association tests 267</p> <p>11.2.2 Choice of a test in applications 272</p> <p>11.2.3 Effect measures 274</p> <p>11.2.4 Selection of the genetic model 280</p> <p>11.2.5 Association tests for the X chromosome 287</p> <p>11.3 Sample size calculation 289</p> <p>11.4 Population stratification 291</p> <p>11.4.1 Testing for population stratification 293</p> <p>11.4.2 Structured association 294</p> <p>11.4.3 Genomic control 295</p> <p>11.4.4 Comparison of structured association and genomic control 297</p> <p>11.4.5 Principal components analysis 297</p> <p>11.5 Gene-gene and gene-environment interaction 299</p> <p>11.5.1 Classical examples for gene-gene and gene-environment interaction 299</p> <p>11.5.2 Coat color in the Labrador retriever 301</p> <p>11.5.3 Concepts of interaction 303</p> <p>11.5.4 Statistical testing of gene-environment interactions 307</p> <p>11.5.5 Statistical testing of gene-gene interactions 311</p> <p>11.5.6 Multifactor dimensionality reduction 315</p> <p>11.6 Problems 316</p> <p><b>12 Family-based Association Analysis 319</b></p> <p>12.1 Haplotype relative risk 320</p> <p>12.2 Transmission disequilibrium test (TDT) 322</p> <p>12.3 Risk estimates for trio data 325</p> <p>12.4 Sample size and power calculations for the TDT 327</p> <p>12.5 Alternative test statistics 329</p> <p>12.6 TDT for multiallelic markers 330</p> <p>12.6.1 Test of single alleles 330</p> <p>12.6.2 Global test statistics 331</p> <p>12.7 TDT type tests for different family structures 333</p> <p>12.7.1 TDT type tests for missing parental data 334</p> <p>12.7.2 TDT type tests for sibship data 336</p> <p>12.7.3 TDT type tests for extended pedigrees 341</p> <p>12.8 Association analysis for quantitative traits 344</p> <p>12.9 Problems 346</p> <p><b>13 Haplotypes in Association Analyses 349</b></p> <p>13.1 Reasons for studying haplotypes 350</p> <p>13.2 Inference of haplotypes 351</p> <p>13.2.1 Algorithms for haplotype assignment 352</p> <p>13.2.2 Algorithms for estimating haplotype probabilities 353</p> <p>13.3 Association tests using haplotypes 356</p> <p>13.4 Haplotype blocks and tagging SNPs 359</p> <p>13.4.1 Selection of markers by haplotypes or linkage disequilibrium 360</p> <p>13.4.2 Evaluation of marker selection approaches 363</p> <p>13.5 Problems 364</p> <p><b>14 Genome-wide Association (GWA) Studies 367</b></p> <p>14.1 Design options in GWA studies 369</p> <p>14.2 Genotype imputation 370</p> <p>14.2.1 Imputation algorithms 370</p> <p>14.2.2 Quality of imputation 371</p> <p>14.3 Statistical analysis of GWA studies 372</p> <p>14.4 Multiple testing 374</p> <p>14.4.1 Region-wide multiple testing adjustment by simulation 375</p> <p>14.4.2 Genome-wide multiple testing adjustment by simulation 376</p> <p>14.4.3 Multiple testing adjustment by effective number of tests 377</p> <p>14.5 Analysis of accumulating GWA data 378</p> <p>14.5.1 Multistage designs for GWA studies 378</p> <p>14.5.2 Replication in GWA studies 379</p> <p>14.5.3 Meta-analysis of GWA studies 380</p> <p>14.6 Clinical impact of a GWA study 383</p> <p>14.6.1 Evaluation of a genetic predictive test 383</p> <p>14.6.2 Clinical validity of a single genetic marker 385</p> <p>14.6.3 Clinical validity of multiple genetic markers 386</p> <p>14.7 Outlook 389</p> <p>14.8 Problems 391</p> <p>Appendix</p> <p>Algorithms Used in Linkage Analyses 393</p> <p>A.1 The Elston–Stewart algorithm 394</p> <p>A.1.1 The fundamental ideas of the Elston–Stewart algorithm 394</p> <p>A.1.2 The Elston–Stewart algorithm for a trait and a linked marker locus 400</p> <p>A.2 The Lander–Green algorithm 401</p> <p>A.2.1 The inheritance vector at a single genetic marker 401</p> <p>A.2.2 The inheritance distribution given all genetic markers 405</p> <p>A.3 The Cardon–Fulker algorithm 412</p> <p>A.4 Problem 414</p> <p>Solutions 415</p> <p>References 451</p> <p>Index 489</p>
<p>“This is a well-written, quality addition to the literature. It is an excellent resource/textbook for those wanting to teach genetic epidemiology as well as those wishing to learn the basics of genetic epidemiology. The new edition improves on the previous edition and expands on necessary topics that have grown in importance over the last five years.”  (<i>Doody’s</i>, 4 January 2013)</p>
<b>Andreas Ziegler</b> is head of the Institute for Medical Biometry and Statistics at the University Clinic Schleswig-Holstein in Lubeck, an acknowledged center of excellence for genetic epidemiological methods. Currently he is President of the German Region of the International Biometric Society. </p> <p><b>Inke R. Konig</b> studied psychology at the universities of Marburg (Germany) as a scholar of the German National Academic Foundation and Dundee (Scotland) with a grant from the German Academic Exchange Service (DAAD). She has done research work at the Institute of Medical Biometry and Epidemiology in Marburg and since 2001 at the Institute of Medical Biometry and Statistics in Lubeck. In 2004, she became vice director of the latter and also received the Fritz-Linder-Forum-Award from the German Association for Surgery. Besides holding the certificate “Biometrics in Medicine”, she has collected teaching experience since 1998 as a lecturer for biomathematics, behavioural genetics, clinical epidemiology, genetic epidemiology, and evidence-based medicine. <p><b>Friedrich Pahlke</b> is Dipl. Inf. at the Institute for Medical Biometry and Statistics at the University Clinic Schleswig-Holstein in Lubeck. He has created the e-learning course which is optionally available with the book.
<p>After studying statistics and mathematics at the University of Munich and obtaining his doctoral degree from the University of Dortmund, <b>Andreas Ziegler</b> received the Johann-Peter-Süssmilch-Medal of the German Association for Medical Informatics, Biometry and Epidemiology for his post-doctoral work on “Model Free Linkage Analysis of Quantitative Traits” in 1999. In 2004, he was one of the recipients of the Fritz-Linder-Forum-Award from the German Association for Surgery.</p>

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