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本文引用的文献

1
High-throughput sequencing provides insights into genome variation and evolution in Salmonella Typhi.
Nat Genet. 2008 Aug;40(8):987-93. doi: 10.1038/ng.195. Epub 2008 Jul 27.
2
Genomics technology for assessing soil pollution.
J Biol. 2008 Jul 14;7(6):19. doi: 10.1186/jbiol80.
5
Genome-scale DNA methylation maps of pluripotent and differentiated cells.
Nature. 2008 Aug 7;454(7205):766-70. doi: 10.1038/nature07107. Epub 2008 Jul 6.
6
The beginning of the end for microarrays?
Nat Methods. 2008 Jul;5(7):585-7. doi: 10.1038/nmeth0708-585.
8
Stem cell transcriptome profiling via massive-scale mRNA sequencing.
Nat Methods. 2008 Jul;5(7):613-9. doi: 10.1038/nmeth.1223. Epub 2008 May 30.
9
Mapping and quantifying mammalian transcriptomes by RNA-Seq.
Nat Methods. 2008 Jul;5(7):621-8. doi: 10.1038/nmeth.1226. Epub 2008 May 30.
10
New developments in ancient genomics.
Trends Ecol Evol. 2008 Jul;23(7):386-93. doi: 10.1016/j.tree.2008.04.002. Epub 2008 May 22.

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