MARC Record from harvard_bibliographic_metadata

LEADER: 03291cam a2200421Ia 4500
001 014135030-X
005 20140905185105.0
006 m o d
008 140603s2014 nyua ob 001 0 eng d
015 $aGBB465647$2bnb
016 7 $a016761429$2Uk
020 $a9781493908479 (eBook)
020 $a1493908472 (eBook)
020 $z9781493908462
035 0 $aocn880899899
040 $aRML$cRML$dRML$dGW5XE$dUKMGB$dFTU
050 4 $aQH324.2$b.C556 2014
082 04 $a572.80285$223
245 00 $aClinical bioinformatics$h[electronic resource] /$cedited by Ronald J.A. Trent.
250 $a2nd ed.
260 $aNew York :$bHumana Press ;$bSpringer,$cc2014.
300 $a1 online resource (xi, 326 p.) :$bill. (some col.)
490 1 $aMethods in molecular biology,$x1940-6029 ;$v1168
505 00 $tFrom the phenotype to the genotype via bioinformatics /$rCali E. Willet and Claire M. Wade --$tProduction and analytic bioinformatics for next-generation DNA sequencing /$rRichard James Nigel Allcock --$tAnalyzing the metabolome /$rFrancis G. Bowling and Mervyn Thomas --$tStatistical perspectives for genome-wide association studies (GWAS) /$rJennifer H. Barrett, John C. Taylor, and Mark M. Iles --$tBioinformatics challenges in genome-wide association studies (GWAS) /$rRishika De, William S. Bush, and Jason H. Moore --$tStudying cancer genomics through next-generation DNA sequencing and bioinformatics /$rMaria A. Doyle ... [et al.] --$tUsing bioinformatics tools to study the role of microRNA in cancer /$rFabio Passetti ... [et al.] --$tChromosome microarrays in diagnostic testing : interpreting the genomic data /$rGreg B. Peters and Mark D. Pertile --$tBioinformatics approach to understanding interacting pathways in neuropsychiatric disorders /$rAli Alawieh ... [et al.] --$tPathogen genome bioinformatics /$rVitali Sintchenko and Michael P. V. Roper --$tSetting up next-generation sequencing in the medical laboratory /$rBing Yu --$tManaging incidental findings in exome sequencing for research /$rMarcus J. Hinchcliffe --$tApproaches for classifying DNA variants found by sanger sequencing in a medical genetics laboratory /$rPak Leng Cheong and Melody Caramins --$tDesigning algorithms for determining significance of DNA missense changes /$rSivakumar Gowrisankar and Matthew S. Lebo --$tDNA variant databases : current state and future directions /$rJohn-Paul Plazzer and Finlay Macrae --$tNatural language processing in biomedicine : a unified system architecture overview /$rSon Doan ... [et al.] --$tCandidate gene discovery and prioritization in rare diseases /$rAnil G. Jegga --$tComputer-aided drug designing /$rMohini Gore and Neetin S. Desai.
504 $aIncludes bibliographical references and index.
650 0 $aBioinformatics.
650 0 $aComputational biology.
650 0 $aGenomics$xData processing.
650 12 $aComputational Biology$xmethods.
650 22 $aDatabases, Genetic.
650 22 $aGenomics.
650 22 $aMedical Informatics Computing.
650 22 $aSequence Analysis, DNA.
700 1 $aTrent, R. J.
776 08 $iPrint version:$tClinical bioinformatics.$dNew York : Humana, c2014$w(OCoLC)872342191
830 0 $aMethods in molecular biology (Clifton, N.J.) ;$vv. 1168.
988 $a20140807
906 $0OCLC