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Design, Analysis, and Interpretation of Genome-Wide Association Scans

Springer New York,
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This book surveys statistical aspects of designing, analyzing and interpreting results of genome-wide association scans for genetic causes of disease, using unrelated subjects. Covers bioinformatics and data handling methods needed to ready data for analysis.

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Titel: Design, Analysis, and Interpretation of Genome-Wide Association Scans
Autoren/Herausgeber: Daniel O. Stram
Aus der Reihe: Statistics for Biology and Health
Ausgabe: 2014

ISBN/EAN: 9781461494423

Seitenzahl: 334
Format: 23,5 x 15,5 cm
Produktform: Hardcover/Gebunden
Gewicht: 726 g
Sprache: Englisch

Dr. Stram’s interests center on the application of modern statistical methods to epidemiologic studies: his research includes methods in longitudinal analysis, meta-analysis, survival analysis, and the analysis of errors in exposure measurement and he is well known for his work on the Atomic Bomb survivors study, the Colorado Plateau Uranium Miners study, the Multiethnic Cohort study and on clinical trials of childhood cancer. He has been an investigator and collaborator on many large scale genetic association studies with an emphasis on multi-ethnic analyses, and has published widely on haplotype analysis, analysis of hidden population structure, and the design of multi-stage genotyping and genome-wide association studies.

This book presents the statistical aspects of designing, analyzing and interpreting the results of genome-wide association scans (GWAS studies) for genetic causes of disease using unrelated subjects. Particular detail is given to the practical aspects of employing the bioinformatics and data handling methods necessary to prepare data for statistical analysis. The goal in writing this book is to give statisticians, epidemiologists, and students in these fields the tools to design a powerful genome-wide study based on current technology. The other part of this is showing readers how to conduct analysis of the created study.Design and Analysis of Genome-Wide Association Studies provides a compendium of well-established statistical methods based upon single SNP associations. It also provides an introduction to more advanced statistical methods and issues. Knowing that technology, for instance large scale SNP arrays, is quickly changing, this text has significant lessons for future use with sequencing data. Emphasis on statistical concepts that apply to the problem of finding disease associations irrespective of the technology ensures its future applications. The author includes current bioinformatics tools while outlining the tools that will be required for use with extensive databases from future large scale sequencing projects. The author includes current bioinformatics tools while outlining additional issues and needs arising from the extensive databases from future large scale sequencing projects.

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