
Bioinformatics and Functional Genomics
$221.59
- Hardcover
1168 pages
- Release Date
15 October 2015
Summary
The bestselling introduction to bioinformatics and genomics – now in its third edition
Widely received in its previous editions, Bioinformatics and Functional Genomics offers the most broad-based introduction to this explosive new discipline. Now in a thoroughly updated and expanded third edition, it continues to be the go-to source for students and professionals involved in biomedical research.
This book provides up-to-the-minute coverage of the fields of bioinformatics and …
Book Details
ISBN-13: | 9781118581780 |
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ISBN-10: | 1118581784 |
Author: | Jonathan Pevsner |
Publisher: | John Wiley and Sons Ltd |
Imprint: | Wiley-Blackwell |
Format: | Hardcover |
Number of Pages: | 1168 |
Edition: | 3rd |
Release Date: | 15 October 2015 |
Weight: | 2.50kg |
Dimensions: | 279mm x 218mm x 48mm |
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About The Author
Jonathan Pevsner
Jonathan Pevsner, PhD, is a Professor in the Department of Neurology at Kennedy Krieger Institute, an internationally recognized institution dedicated to improving the lives of children with neurodevelopmental disorders. He holds a primary faculty appointment as Professor in the Department of Psychiatry and Behavioral Sciences (Johns Hopkins University School of Medicine). He holds joint or secondary appointments in the Department of Neuroscience, the Institute of Genetic Medicine, and the Division of Health Sciences Informatics (Johns Hopkins School of Medicine), and the Department of Molecular Microbiology and Immunology (Johns Hopkins Bloomberg School of Public Health). He has taught bioinformatics courses since 2000 at the Johns Hopkins School of Medicine, and was awarded Teacher of the Year honors by the Graduate Student Association in both 2001 and 2006, the Professors’ Award for Excellence in Teaching awarded by the medical faculty (2003), Teacher of the Year (Advanced Academic Programs, 2009), and Teaching Excellence Award in the Johns Hopkins Bloomberg School of Public Health (2011). In 2013 his lab used whole genome sequencing and reported a mutation that causes a rare disease, Sturge-Weber syndrome, as well as a commonly occurring port-wine stain birthmark.
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