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Computational Genetics And AGenomics: Tools for Understanding Disease

Contributor(s): Peltz, Gary. (Editor).
Material type: materialTypeLabelBookPublisher: U.S.A: Humana Press; 2005Edition: 1st.Description: 308 p.ISBN: 1588291871 (hardcover); 9781588291875 (hardcover).Subject(s): Genetics Genomics-Mathematical models Medicine Human genetics GenomicsDDC classification: 611.01816 Peltz 20007 1st 2005 Genetics Summary: Ultimately, the quality of the tools available for genetic analysis and experimental disease models will be assessed on the basis of whether they provide new information that generates novel treatments for human disease. In addition, the time frame in which genetic discoveries impact clinical practice is also an important dimension of how society assesses the results of the significant public financial investment in genetic research. Because of the investment and the increased expectation that new tre- ments will be found for common diseases, allowing decades to pass before basic discoveries are made and translated into new therapies is no longer acceptable. Computational Genetics and Genomics: Tools for Understanding Disease provides an overview and assessment of currently available and developing tools for genetic analysis. It is hoped that these new tools can be used to identify the genetic basis for susceptibility to disease. Although this very broad topic is addressed in many other books and journal articles, Computational Genetics and Genomics: Tools for Understanding Disease focuses on methods used for analyzing mouse genetic models of biomedically - portant traits. This volume aims to demonstrate that commonly used inbred mouse strains can be used to model virtually all human disea- related traits. Importantly, recently developed computational tools will enable the genetic basis for differences in disease-related traits to be rapidly identified using these inbred mouse strains. On average, a decade is required to carry out the development process required to demonstrate that a new disease treatment is beneficial.
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Veterinary Science 611.01816 Peltz 20007 1st 2005 Genetics (Browse shelf) Available 20007
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610.28 Xie 1s 2013 30010 Genetics The Nanobiotechnology Handbook 611.0181 Cummings 28918 1st 2009 Genetics Human Genetics 611.0181 Cummings 25066 1st 2009 Genetics Human Genetics 611.01816 Peltz 20007 1st 2005 Genetics Computational Genetics And AGenomics: Tools for Understanding Disease 611.01816 Strachan 32456 4th 2011 Genetics Human molecular genetics 611.01816 Strachan 33879 5th 2019 Genetics Human Molecular Genetics 5th ed 612.01 Guthrie 20832 Vol.B 2002 Genetics Guide to Yeast Genetics and Molecular and Cell Biology/ Vol.350

Ultimately, the quality of the tools available for genetic analysis and experimental disease models will be assessed on the basis of whether they provide new information that generates novel treatments for human disease. In addition, the time frame in which genetic discoveries impact clinical practice is also an important dimension of how society assesses the results of the significant public financial investment in genetic research. Because of the investment and the increased expectation that new tre- ments will be found for common diseases, allowing decades to pass before basic discoveries are made and translated into new therapies is no longer acceptable. Computational Genetics and Genomics: Tools for Understanding Disease provides an overview and assessment of currently available and developing tools for genetic analysis. It is hoped that these new tools can be used to identify the genetic basis for susceptibility to disease. Although this very broad topic is addressed in many other books and journal articles, Computational Genetics and Genomics: Tools for Understanding Disease focuses on methods used for analyzing mouse genetic models of biomedically - portant traits. This volume aims to demonstrate that commonly used inbred mouse strains can be used to model virtually all human disea- related traits. Importantly, recently developed computational tools will enable the genetic basis for differences in disease-related traits to be rapidly identified using these inbred mouse strains. On average, a decade is required to carry out the development process required to demonstrate that a new disease treatment is beneficial.

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