Yearbook of Medical Informatics, Table of Contents Yearb Med Inform 2013; 22(01): 175-177DOI: 10.1055/s-0038-1638852 Original Article Georg Thieme Verlag KG StuttgartFrom Genome Sequencing to BedsideFindings from the Section on Bioinformatics and Translational InformaticsAuthors Author Affiliations Section Editors for the IMIA Yearbook Section on Bioinformatics and Translational Informatics T. Lecroq 1 Normandie University, University of Rouen, LITIS EA 4108, Information Processing in Biology & Health, Mont-Saint-Aignan, France L. F. Soualmia 1 Normandie University, University of Rouen, LITIS EA 4108, Information Processing in Biology & Health, Mont-Saint-Aignan, France Recommend Article Abstract Full Text PDF Download(opens in new window) Keywords KeywordsTranslational Medical Research - Computational Biology - Gene expression - Genome - Medical Informatics References References 1 Yip YL. Unlocking the potential of electronic health records for translational research. Findings from the section on the bioinformatics and translational informatics. Yearb Med Inform 2012; 7 (1) 135-8. 2 Sanger F, Coulson AR. A rapid method for determining sequences in DNA by primed synthesis with DNA polymerase. J Mol Biol 1975; 94 (3) 441-8. 3 Kohane IS, Churchill SE, Murphy SN. A translational engine at the national scale: informatics for integrating biology and the bedside. J Am Med Inform Assoc 2012; Mar-Apr 19 (2) 181-5. 4 Roden DM, Xu H, Denny JC, Wilke RA. Electronic medical records as a tool in clinical pharmacology: opportunities and challenges. Clin Pharmacol Ther 2012; Jun 91 (6) 1083-6. 5 Liu ZP, Wang Y, Zhang XS, Chen L. Network-based analysis of complex diseases. IET Syst Biol 2012; Feb 6 (1) 22-33. 6 Harrow J, Frankish A, Gonzalez JM, Tapanari E, Diekhans M, Kokocinski F. et al. GENCODE: the reference human genome annotation for The ENCODE Project. Genome Res 2012; Sep 22 (9) 1760-74. 7 Stubbs A, McClellan EA, Horsman S, Hiltemann SD, Palli I, Nouwens S. et al. Huvariome: a web server resource of whole genome next-generation sequencing allelic frequencies to aid in pathological candidate gene selection. J Clin Bioinforma 2012; Nov 19 2 (1) 19. 8 Tennessen JA, Bigham AW, O'Connor TD, Fu W, Kenny EE, Gravel S. et al NHLBI Exome Sequencing Project. Evolution and functional impact ofrare coding variation from deep sequencing of human exomes. Science 2012; Jul 6 337 (6090) 64-9. 9 Tian Q, Price ND, Hood L. Systems cancer medicine: towards realization of predictive, preventive, personalized and participatory (P4) medicine. J Intern Med 2012; Feb 271 (2) 111-21. 10 Akan P, Alexeyenko A, Costea PI, Hedberg L, Solnestam BW, Lundin S. et al. Comprehensive analysis ofthe genome transcriptome and proteome landscapes of three tumor cell lines. Genome Med 2012; Nov 18 4 (11) 86. 11 Leary RJ, Sausen M, Kinde I, Papadopoulos N, Carpten JD, Craig D. et al. Detection of chromosomal alterations in the circulation of cancer patients with whole-genome sequencing. Sci Transl Med. 2012 Nov 28 4. (162) 162ra154. 12 The ENCODE Project Consortium. A user's guide to the ENCyclopedia Of DNA Elements (ENCODE). PLoS Biol. 2011 9. (4) e1001046.
