Figures and Tables

From the following article:

The complete genome of an individual by massively parallel DNA sequencing

David A. Wheeler, Maithreyan Srinivasan, Michael Egholm, Yufeng Shen, Lei Chen, Amy McGuire, Wen He, Yi-Ju Chen, Vinod Makhijani, G. Thomas Roth, Xavier Gomes, Karrie Tartaro, Faheem Niazi, Cynthia L. Turcotte, Gerard P. Irzyk, James R. Lupski, Craig Chinault, Xing-zhi Song, Yue Liu, Ye Yuan, Lynne Nazareth, Xiang Qin, Donna M. Muzny, Marcel Margulies, George M. Weinstock, Richard A. Gibbs & Jonathan M. Rothberg

Nature 452, 872-876(17 April 2008)

doi:10.1038/nature06884

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Figure 1

454-Sequencing of individual genome generated even coverage enabling genome-wide detection of variation.

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Table 1

Single nucleotide variation in 454 reads

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Table 2

Microarray validation of 454 SNPs

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Table 3

SNPs matching HGMD mutations causing disease or other phenotypes

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