Item Details
Clinical Bioinformatics [electronic resource]
edited by Ronald Trent, Department of Medical Genomics, Royal Prince Alfred Hospital and Sydney Medical School, University of Sydney, Camperdown, Australia
- Format
- EBook; Book; Online
- Published
- New York : Humana Press, [2014]
- Edition
- Second Edition
- Language
- English
- Series
- Methods in Molecular Medicine
- ISBN
- 9781493908462 (alk. paper), 1493908464 (alk. paper), 9781493908479 (eBook), 1493908472 (eBook)
- Contents
- From the phenotype to the genotype via bioinformatics / Cali E. Willet and Calire M. Wade
- Production and analytic bioinformatics for next-generation DNA sequencing / Richard James, Nigel Allcock
- Analyzing the metabolome / Fracnis G. Bowling and Mervyn Thomas
- Statistical perspectives for Genome-Wide Association Studies (GWAS) / Jennifer H. Barrett, John C. Taylor, and Mark M. Iles
- Bioinformatics challenges in Genome-Wide Association Studies (GWAS) / Rishika De, William S. Bush, and Jason H. Morre
- Studying cancer genomics through next-generation DNA sequencing and bioinformatics / Maraia A. Doyle, Jason LI, Ken Doig, Andrew Fellowes, and Stephen Q. Wong - Using bioinformatics tools to study the role of microRNA in cancer / Fabio Passetti, Natasha Andressa Noguiera Jorge, and Alan Durham
- Chromosome microarrays in diagnostic testing : interpreting the genomic data / Greg B. Peters and Mark D. Pertile
- Bioinformatics approach to understanding interacting pathways in neuropsychiatric disorders / Ali Alawieh, Zahraa Sabra, Amaly Nokkari, Atlal El-Assaad, Stefania Mondello, Fadi Zaraket, Bilal Fadlallah, and Firas H. Kobeissy
- Pathogen genome bioinformatics / Vitali Sintchenko and Michael P.V. Roper
- Setting up next-generation sequencing in the medical laboratory / Bing Yu
- Managing Incidental findings in Exome sequencing for research / Marcus J. Hinch cliffe
- Approaches for classifying DNA variants found by Sanger sequencing in Medical Genetics Laboratory / Pak Leng Cheong and Melody Caramins
- Designing algorithms for determining significance of DNA Missense changes / Sivakumar Gowrisankar and Matthew S. Lebo
- DNA variant databases : current state and future directions / John-Paul Plazzer and Finalay Macrae
- Natural language processing in biomedecine : a unified system architecture overview / Son Doan, Mike Conway, Tu Minh Phuong, and Lucila Ohno-Machado
- Candidate gene discovery and prioritization in rare diseases / Anil G. Jegga
- Computer-aided drug designing / Mohini Gore and Neetin S. Desai.
- Description
- Mode of access: World wide Web.
- Series Statement
- Methods in molecular medicine, 1064-3745 ; 1168
- Copyright & Permissions
Copyright Not Evaluated- Technical Details
-
- Access in Virgo Classic
- Staff View
LEADER 03454cam a2200385 i 4500001 u6440235003 SIRSI005 20160208132457.0006 m d007 cr n008 140430s2014 njua sb 001 0 eng da| 2014939636a| 9781493908462 (alk. paper)a| 1493908464 (alk. paper)z| 9781493908479 (eBook)z| 1493908472 (eBook)a| (WaSeSS)ssj0001371300a| DLC b| eng c| DLC d| DLC d| WaSeSSa| QH324.2 b| .C556 2014a| 610.285 2| 23a| Clinical bioinformatics h| [electronic resource] / c| edited by Ronald Trent, Department of Medical Genomics, Royal Prince Alfred Hospital and Sydney Medical School, University of Sydney, Camperdown, Australia.a| Second Edition.a| New York : b| Humana Press, c| [2014]a| Methods in molecular medicine, x| 1064-3745 ; v| 1168a| From the phenotype to the genotype via bioinformatics / Cali E. Willet and Calire M. Wade -- Production and analytic bioinformatics for next-generation DNA sequencing / Richard James, Nigel Allcock -- Analyzing the metabolome / Fracnis G. Bowling and Mervyn Thomas -- Statistical perspectives for Genome-Wide Association Studies (GWAS) / Jennifer H. Barrett, John C. Taylor, and Mark M. Iles -- Bioinformatics challenges in Genome-Wide Association Studies (GWAS) / Rishika De, William S. Bush, and Jason H. Morre -- Studying cancer genomics through next-generation DNA sequencing and bioinformatics / Maraia A. Doyle, Jason LI, Ken Doig, Andrew Fellowes, and Stephen Q. Wong - Using bioinformatics tools to study the role of microRNA in cancer / Fabio Passetti, Natasha Andressa Noguiera Jorge, and Alan Durham -- Chromosome microarrays in diagnostic testing : interpreting the genomic data / Greg B. Peters and Mark D. Pertile -- Bioinformatics approach to understanding interacting pathways in neuropsychiatric disorders / Ali Alawieh, Zahraa Sabra, Amaly Nokkari, Atlal El-Assaad, Stefania Mondello, Fadi Zaraket, Bilal Fadlallah, and Firas H. Kobeissy -- Pathogen genome bioinformatics / Vitali Sintchenko and Michael P.V. Roper -- Setting up next-generation sequencing in the medical laboratory / Bing Yu -- Managing Incidental findings in Exome sequencing for research / Marcus J. Hinch cliffe -- Approaches for classifying DNA variants found by Sanger sequencing in Medical Genetics Laboratory / Pak Leng Cheong and Melody Caramins -- Designing algorithms for determining significance of DNA Missense changes / Sivakumar Gowrisankar and Matthew S. Lebo -- DNA variant databases : current state and future directions / John-Paul Plazzer and Finalay Macrae -- Natural language processing in biomedecine : a unified system architecture overview / Son Doan, Mike Conway, Tu Minh Phuong, and Lucila Ohno-Machado -- Candidate gene discovery and prioritization in rare diseases / Anil G. Jegga -- Computer-aided drug designing / Mohini Gore and Neetin S. Desai.a| Mode of access: World wide Web.a| Bioinformatics.a| Computational biology.a| Genomics x| Data processing.a| Electronic books.a| Trent, R. J.a| Springer Protocolsu| http://RE5QY4SB7X.search.serialssolutions.com/?V=1.0&L=RE5QY4SB7X&S=JCs&C=TC0001371300&T=marca| 1a| XX(6440235.1) w| WEB i| 6440235-1001 l| INTERNET m| UVA-LIB t| INTERNET
