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A Statistical approach to genetic epidemiology : concepts and applications, with an e-Learning Platform.
This is the second edition of the successful textbook written by the prize-winning scientist Andreas Ziegler, former President of the German Region of the International Biometric Society, and Inke R. König, who has been teaching the subject over many years. The book gives a comprehensive introducti...
| Clasificación: | Libro Electrónico |
|---|---|
| Autor principal: | |
| Otros Autores: | , |
| Formato: | Electrónico eBook |
| Idioma: | Inglés |
| Publicado: |
Weinheim :
John Wiley & Sons,
2012.
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| Edición: | 4th ed. |
| Temas: | |
| Acceso en línea: | Texto completo |
Tabla de Contenidos:
- Cover; title; Copyright; Dedication; Preface; Acknowledgments; 1: Molecular Genetics; 1.1 WHAT IS THE NATURE OF GENETIC INFORMATION?; 1.2 HOW IS GENETIC INFORMATION TRANSMITTED FROM GENERATION TO GENERATION?; 1.3 WHAT IS INDIVIDUAL VARIATION IN GENETIC INFORMATION?; 1.4 PROBLEMS; URLs; 2: Formal Genetics; 2.1 WHAT ARE MENDEL'S LAWS?; 2.2 HOW ARE PHENOTYPES TRANSMITTED IN FAMILIES?; 2.3 WHICH COMPLICATIONS TO THE GENERAL INHERITANCE PATTERNS EXIST?; 2.4 WHAT IS THE LAW DETECTED BY HARDY AND WEINBERG?; 2.5 PROBLEMS; URLs; 3: Genetic Markers; 3.1 WHAT IS A GENETIC MARKER?
- 3.2 WHAT TYPES OF GENETIC MARKERS ARE THERE?3.3 WHAT ARE GENOTYPING METHODS FOR SINGLE NUCLEOTIDE POLYMORPHISMS?; 3.4 PROBLEMS; URLs; 4: Data Quality; 4.1 HOW CAN PEDIGREE ERRORS BE DETECTED?; 4.2 HOW CAN GENOTYPING ERRORS BE DETECTED IN FAMILY-BASED STUDIES?; 4.3 HOW SHOULD GENOTYPING ERRORS BE CHECKED IN POPULATION-BASED STUDIES USING THE HARDY-WEINBERG EQUILIBRIUM?; Algorithm 4.1.; Algorithm 4.2.; Algorithm 4.3.; 4.4 HOW CAN GENOTYPING ERRORS BE DETECTED IN HIGH-THROUGHPUT GENOTYPING STUDIES?
- 4.5 HOW SHOULD CLUSTER PLOTS AND HOW CAN THE QUALITY OF CLUSTERS BE INVESTIGATED IN HIGH-THROUGHPUT GENOTYPING STUDIES?4.6 PROBLEMS; URLs; 5: Genetic Map Distances; 5.1 WHAT IS PHYSICAL DISTANCE?; 5.2 WHAT IS MAP DISTANCE?; 5.3 WHAT ARE LINKAGE DISEQUILIBRIUM UNITS?; 5.4 PROBLEMS; URLs; 6: Familiality, Heritability, and Segregation Analysis; 6.1 WHAT IS THE DIFFERENCE BETWEEN THE FAMILY HISTORY METHOD AND THE FAMILY STUDY METHOD?; 6.2 HAS THE PHENOTYPE OF INTEREST A FAMILIAL COMPONENT? WHAT ARE RECURRENCE RISK RATIOS?; 6.3 WHAT IS THE CONCEPT OF HERITABILITY?
- 6.4 WHAT ARE TWIN STUDIES? WHAT ARE ADOPTION STUDIES?6.5 WHAT ARE CRITICAL ASPECTS WHEN INVESTIGATING FAMILIAL RESEMBLANCE?; 6.6 HOW CAN EVIDENCE FOR A MAJOR GENE EFFECT BE ESTABLISHED? HOW CAN A SEGREGATION PATTERN FOLLOWING MENDELIAN INHERITANCE BE DETERMINED?; 6.7 PROBLEMS; URLs; 7: Model-Based Linkage Analysis; 7.1 HOW CAN THE RECOMBINATION FRACTION BE ESTIMATED BETWEEN TWO GENETIC MARKERS?; 7.2 HOW CAN THE RECOMBINATION FRACTION BE ESTIMATED BETWEEN A GENETIC MARKER AND A DISEASE?; 7.3 WHAT IS SIGNIFICANT EVIDENCE OF LINKAGE?; 7.4 PROBLEMS; URLs
- 8: Model-Free Linkage Analysis for Dichotomous Traits8.1 WHAT IS THE BASIC IDEA OF MODEL-FREE LINKAGE ANALYSIS?; 8.2 WHY IS AFFECTED SIB-PAIR ANALYSIS REASONABLE?; 8.3 WHAT ARE COMMON TESTS FOR AFFECTED SIB-PAIR ANALYSIS?; 8.4 IS THERE AN OPTIMAL AFFECTED SIB-PAIR TEST? ARE AFFECTED SIB-PAIR TESTS RELATED TO MODEL-BASED LINKAGE TESTS?; 8.5 HOW CAN SAMPLE SIZE OR POWER BE CALCULATED FOR AN AFFECTED SIB-PAIR STUDY?; 8.6 HOW ARE MODEL-FREE METHODS EXTENDED TO MULTIPLE MARKER LOCI?; 8.7 WHAT ARE STANDARD APPROACHES FOR THE ANALYSIS OF LARGE SIBSHIPS?