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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 Not EvaluatedCopyright Not Evaluated
Technical Details
  • Access in Virgo Classic
  • Staff View

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    a| 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.
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