Human Evolutionary Genetics, Second Edition

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Now in full-color, the Second Edition of Human Evolutionary Genetics has been completely revised to cover the rapid advances in the field since publication of the highly regarded First Edition. Written for upper-level undergraduate and graduate students, it is the only textbook to integrate genetic, archaeological, and linguistic perspectives on human evolution, and to offer a genomic perspective, reflecting the shift from studies of specific regions of the genome towards comprehensive genomewide analyses of human genetic diversity.
Human Evolutionary Genetics is suitable for courses in Genetics, Evolution, and Anthropology. Those readers with a background in anthropology will find that the streamlined genetic analysis material contained in the Second Edition is more accessible. The new edition also integrates new technologies (including next-generation sequencing and genome-wide SNP typing) and new data analysis methods, including recent data on ancient genomes and their impact on our understanding of human evolution. The book also examines the subject of personal genomics and its implications.
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About the author

Mark Joblingearned a degree in Biochemistry and a DPhil at the University of Oxford, UK, and in 1992 came to the University of Leicester, UK, where he is now a Wellcome Trust Senior Fellow in Basic Biomedical Sciences and Reader in Genetics. Mark's interests are in Y chromosome diversity as a tool for addressing questions in human evolution, genealogy and forensics, and also male infertility and haploid mutation processes.

Matthew Hurlesearned his degree in biochemistry at Oxford University, UK, and PhD in Leicester, UK. He was until recently a Research Fellow at the McDonald Institute for Archaeological Research at Cambridge University, UK, analyzing genetic variation with the aim of improving our understanding of the human past. He is now at the Wellcome Trust Sanger Institute near Cambridge, UK, investigating the unusual evolutionary dynamics of recently duplicated genomic regions.

Chris Tyler-Smithearned his degree in biochemistry at Oxford University, UK, and PhD in Edinburgh, UK. For the last few years he has been a University Research Lecturer in the Biochemistry Department at Oxford, UK, working on the structure and function of human centromeres, and the application of Y-chromosomal DNA variation to the understanding of the human past. He is now at the Wellcome Trust Sanger Institute near Cambridge, UK, studying the genetic changes that have taken place during recent human evolution.

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Additional Information

Garland Science
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Published on
Jun 23, 2013
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Best For
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Science / Life Sciences / Genetics & Genomics
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Content Protection
This content is DRM protected.
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Eligible for Family Library

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