MARC Record from Library of Congress

LEADER: 03179cam a2200313 i 4500
001 2014939636
003 DLC
005 20151205083328.0
008 140430s2014 njua b 001 0 eng
010 $a 2014939636
020 $a9781493908462 (alk. paper)
020 $a1493908464 (alk. paper)
020 $z9781493908479 (eBook)
020 $z1493908472 (eBook)
040 $aDLC$beng$erda$cDLC$dDLC
050 00 $aQH324.2$b.C556 2014
245 00 $aClinical bioinformatics /$cedited by Ronald Trent, Department of Medical Genomics, Royal Prince Alfred Hospital and Sydney Medical School, University of Sydney, Camperdown, Australia.
250 $aSecond Edition.
264 1 $aNew York :$bHumana Press,$c[2014]
300 $axi, 326 pages :$billustrations (some color) ;$c24 cm
336 $atext$btxt$2rdacontent
337 $aunmediated$bn$2rdamedia
338 $avolume$bnc$2rdacarrier
490 0 $aMethods in molecular medicine,$x1064-3745 ;$v1168
505 0 $aFrom 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.
650 0 $aBioinformatics.
650 0 $aComputational biology.
650 0 $aGenomics$xData processing.
700 1 $aTrent, R. J.,$eeditor.