Next generation DNA sequencing and the future of genomic medicine.
作者： Matthew W. Anderson , Iris Schrijver
DOI: 10.3390/GENES1010038
关键词:
摘要: … for sequencing 100 human genomes in 10 days for less than $10,000 per genome [26], a few groups have proposed alternative sequencing methods that determine the sequence of the …
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Peter Kraft, David G. Cox, Study designs for genome-wide association studies. Advances in Genetics. ,vol. 60, pp. 465- 504 ,(2008) , 10.1016/S0065-2660(07)00417-8
TE Klein, RB Altman, Niclas Eriksson, BF Gage, SE Kimmel, MT Lee, NA Limdi, D Page, DM Roden, MJ Wagner, MD Caldwell, JA Johnson, YT Chen, MS Wen, Y Caraco, I Achache, S Blotnick, M Muszkat, JG Shin, HS Kim, G Suarez-Kurtz, JA Perini, E Silva-Assuncao, JL Anderson, BD Horne, JF Carlquist, RL Berg, JK Burmester, BC Goh, SC Lee, F Kamali, E Sconce, AK Daly, AH Wu, TY Langaee, H Feng, L Cavallari, K Momary, M Pirmohamed, A Jorgensen, CH Toh, P Williamson, H McLeod, JP Evans, KE Weck, C Brensinger, Y Nakamura, T Mushiroda, D Veenstra, L Meckley, MJ Rieder, AE Rettie, M Wadelius, H Melhus, CM Stein, U Schwartz, D Kurnik, E Deych, P Lenzini, C Eby, LY Chen, P Deloukas, A Motsinger-Reif, H Sagreiya, BS Srinivasan, E Lantz, T Chang, M Ritchie, LS Lu, Estimation of the warfarin dose with clinical and pharmacogenetic data The New England Journal of Medicine. ,vol. 360, pp. 753- 764 ,(2009) , 10.1056/NEJMOA0809329
A. S Elstein, Evidence base of clinical diagnosis: Clinical problem solving and diagnostic decision making: selective review of the cognitive literature BMJ. ,vol. 324, pp. 729- 732 ,(2002) , 10.1136/BMJ.324.7339.729
Thomas W White, Michael R Deans, David P Kelsell, David L Paul, None, Connexin mutations in deafness Nature. ,vol. 394, pp. 630- 631 ,(1998) , 10.1038/29202
M. Ronaghi, DNA SEQUENCING:A Sequencing Method Based on Real-Time Pyrophosphate Science. ,vol. 281, pp. 363- 365 ,(1998) , 10.1126/SCIENCE.281.5375.363
Iris Schrijver, Hereditary Non-Syndromic Sensorineural Hearing Loss The Journal of Molecular Diagnostics. ,vol. 6, pp. 275- 284 ,(2004) , 10.1016/S1525-1578(10)60522-3
Jerald P. Radich, Andrew D. Zelenetz, Wing C. Chan, Carlo M. Croce, Myron S. Czuczman, Harry P. Erba, Sandra J. Horning, Jane Houldsworth, B. Douglas Smith, David S. Snyder, Hema M. Sundar, Meir Wetzler, Jane N. Winter, NCCN task force report: molecular markers in leukemias and lymphomas. Journal of The National Comprehensive Cancer Network. ,vol. 7, ,(2009) , 10.6004/JNCCN.2009.0077
J. T. Simpson, K. Wong, S. D. Jackman, J. E. Schein, S. J.M. Jones, I. Birol, ABySS: A parallel assembler for short read sequence data Genome Research. ,vol. 19, pp. 1117- 1123 ,(2009) , 10.1101/GR.089532.108
Lloyd M. Smith, Jane Z. Sanders, Robert J. Kaiser, Peter Hughes, Chris Dodd, Charles R. Connell, Cheryl Heiner, Stephen B. H. Kent, Leroy E. Hood, Fluorescence detection in automated DNA sequence analysis Nature. ,vol. 321, pp. 674- 679 ,(1986) , 10.1038/321674A0
M. Schena, D. Shalon, R. W. Davis, P. O. Brown, Quantitative Monitoring of Gene Expression Patterns with a Complementary DNA Microarray Science. ,vol. 270, pp. 467- 470 ,(1995) , 10.1126/SCIENCE.270.5235.467