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10.1016/j.ygeno.2011.07.006 http://scihub22266oqcxt.onion/10.1016/j.ygeno.2011.07.006 C4074010!4074010!21839162     free     free     free       Genomics 2011 ; 98 (4): 233-41 Nephropedia Template TP {{tp|p=21839162|t=2011. ANNOTATING INDIVIDUAL HUMAN GENOMES* |pdf=|usr=}}{{21839162}} gab.com Text ANNOTATING INDIVIDUAL HUMAN GENOMES* JO: Genomics http://www.kidney.de/pget.php?&tw=1&pmid=21839162 #FOAvip Advances in DNA sequencing technologies have made it possible to rapidly, accurately and affordably sequence entire individual human genomes. As impressive as this ability seems, however, it will not likely to amount to much if one cannot extract meaningful information from individual sequence data. Annotating variations within individual genomes and providing information about their biological or phenotypic impact will thus be crucially important in moving individual sequencing projects forward, especially in the context of the clinical use of sequence information. In this paper we consider the various ways in which one might annotate individual sequence variations and point out limitations in the available methods for doing so. It is arguable that, in the foreseeable future, DNA sequencing of individual genomes will become routine for clinical, research, forensic, and personal purposes. We therefore also consider directions and areas for further research in annotating genomic variants. Twit Text FOAVip ANNOTATING INDIVIDUAL HUMAN GENOMES* ????Genomics http://www.kidney.de/pget.php?&tw=1&pmid=21839162 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=21839162 #FOAvip English Wikipedia <ref>{{Cite pmid|21839162}}</ref> ANNOTATING INDIVIDUAL HUMAN GENOMES* #MMPMID21839162 Torkamani A; Scott-Van Zeeland AA; Topol EJ; Schork NJ Genomics 2011[Oct]; 98 (4): 233-41 PMID21839162show ga Advances in DNA sequencing technologies have made it possible to rapidly, accurately and affordably sequence entire individual human genomes. As impressive as this ability seems, however, it will not likely to amount to much if one cannot extract meaningful information from individual sequence data. Annotating variations within individual genomes and providing information about their biological or phenotypic impact will thus be crucially important in moving individual sequencing projects forward, especially in the context of the clinical use of sequence information. In this paper we consider the various ways in which one might annotate individual sequence variations and point out limitations in the available methods for doing so. It is arguable that, in the foreseeable future, DNA sequencing of individual genomes will become routine for clinical, research, forensic, and personal purposes. We therefore also consider directions and areas for further research in annotating genomic variants. äANNOTATING INDIVIDUAL HUMAN GENOMES* (epmc).pdf DeepDyve Pubget Overpricing