Page 12 - Applied Probability
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Preface to the Second Edition
                              Progress in genetics between the first and second editions of this book has
                              been nothing short of revolutionary. The sequencing of the human genome
                              and other genomes is already having a profound impact on biological re-
                              search. Although the scientific community has only a vague idea of how
                              this revolution will play out and over what time frame, it is clear that large
                              numbers of students from the mathematical sciences are being attracted
                              to genomics and computational molecular biology in response to the latest
                              developments. It is my hope that this edition can equip them with some of
                              the tools they will need.
                                Almost nothing has been removed from the first edition except for a
                              few errors that readers have kindly noted. However, more than 100 pages
                              of new material has been added in the second edition. Most prominent
                              among the additions are new chapters introducing DNA sequence analysis
                              and diffusion processes and an appendix on the multivariate normal dis-
                              tribution. Several existing chapters have also been expanded. Chapter 2
                              now has a section on binding domain identification, Chapter 3 a section
                              on Bayesian estimation of haplotype frequencies, Chapter 4 a section on
                              case-control association studies, Chapter 7 new material on the gamete
                              competition model, Chapter 8 three sections on QTL mapping and factor
                              analysis, Chapter 9 three sections on the Lander-Green-Kruglyak algorithm
                              and its applications, Chapter 10 three sections on codon and rate varia-
                              tion models, and Chapter 14 a better discussion of statistical significance
                              in DNA sequence matches. Sprinkled throughout the chapters are several
                              new problems.
                                I have many people to thank in putting together this edition. It has been
                              a consistent pleasure working with John Kimmel of Springer. Ted Reich
                              kindly helped me in gaining permission to use the COGA alcoholism data
                              in the QTL mapping example of Chapter 8. Many of the same people who
                              assisted with editorial suggestions, data analysis, and problem solutions in
                              the first edition have contributed to the second edition. I would particu-
                              larly like to single out Jason Aten, Lara Bauman, Michael Boehnke, Ruzong
                              Fan, Steve Horvath, David Hunter, Ethan Lange, Benjamin Redelings, Eric
                              Schadt, Janet Sinsheimer, Heather Stringham, and my wife, Genie. As a
                              one-time editor, Genie will particularly appreciate that a comma now ap-
                              pears in my dedication between “wife” and “Genie,” thereby removing any
                              suspicion that I am a polygamist.
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