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Science 25 January 2008:
Vol. 319. no. 5862, p. 395
DOI: 10.1126/science.319.5862.395
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News of the Week

DNA SEQUENCING:
A Plan to Capture Human Diversity in 1000 Genomes

Jocelyn Kaiser

Over the next 3 years, an international team plans to create a massive new catalog containing the complete genome sequences of 1000 individuals. It will help fill out the list of new genetic markers for common diseases that came out in 2007.

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THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES:
Detecting natural selection by empirical comparison to random regions of the genome.
F. Yu, A. Keinan, H. Chen, R. J. Ferland, R. S. Hill, A. A. Mignault, C. A. Walsh, and D. Reich (2009)
Hum. Mol. Genet. 18, 4853-4867
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Effect of read-mapping biases on detecting allele-specific expression from RNA-sequencing data.
J. F. Degner, J. C. Marioni, A. A. Pai, J. K. Pickrell, E. Nkadori, Y. Gilad, and J. K. Pritchard (2009)
Bioinformatics 25, 3207-3212
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A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.
A. C. Need, D. K. Attix, J. M. McEvoy, E. T. Cirulli, K. L. Linney, P. Hunt, D. Ge, E. L. Heinzen, J. M. Maia, K. V. Shianna, et al. (2009)
Hum. Mol. Genet. 18, 4650-4661
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The UCSC genome browser database: update 2010.
B. Rhead, D. Karolchik, R. M. Kuhn, A. S. Hinrichs, A. S. Zweig, P. A. Fujita, M. Diekhans, K. E. Smith, K. R. Rosenbloom, B. J. Raney, et al. (2009)
Nucleic Acids Res.
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De novo sequencing of plant genomes using second-generation technologies.
M. Imelfort and D. Edwards (2009)
Brief Bioinform 10, 609-618
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Sequence and structural variation in a human genome uncovered by short-read, massively parallel ligation sequencing using two-base encoding.
K. J. McKernan, H. E. Peckham, G. L. Costa, S. F. McLaughlin, Y. Fu, E. F. Tsung, C. R. Clouser, C. Duncan, J. K. Ichikawa, C. C. Lee, et al. (2009)
Genome Res. 19, 1527-1541
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Measuring the Rates of Spontaneous Mutation From Deep and Large-Scale Polymorphism Data.
P. W. Messer (2009)
Genetics 182, 1219-1232
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Data structures and compression algorithms for genomic sequence data.
M. C. Brandon, D. C. Wallace, and P. Baldi (2009)
Bioinformatics 25, 1731-1738
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Genomic medicine in Mexico: Initial steps and the road ahead.
G. Jimenez-Sanchez, I. Silva-Zolezzi, A. Hidalgo, and S. March (2008)
Genome Res. 18, 1191-1198
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An MCMC algorithm for haplotype assembly from whole-genome sequence data.
V. Bansal, A. L. Halpern, N. Axelrod, and V. Bafna (2008)
Genome Res. 18, 1336-1346
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The Genome Gets Personal--Almost.
W. G. Feero, A. E. Guttmacher, and F. S. Collins (2008)
JAMA 299, 1351-1352
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Science. ISSN 0036-8075 (print), 1095-9203 (online)