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本文引用的文献
1
Cancer research. Looking for a target on every tumor.
Science. 2009 Oct 9;326(5950):218-20. doi: 10.1126/science.326_218.
2
Mutational evolution in a lobular breast tumour profiled at single nucleotide resolution.
Nature. 2009 Oct 8;461(7265):809-13. doi: 10.1038/nature08489.
3
Recurring mutations found by sequencing an acute myeloid leukemia genome.
N Engl J Med. 2009 Sep 10;361(11):1058-66. doi: 10.1056/NEJMoa0903840. Epub 2009 Aug 5.
4
Exome sequencing takes centre stage in cancer profiling.
Nature. 2009 May 14;459(7244):146-7. doi: 10.1038/459146b.
5
New strategies and emerging technologies for massively parallel sequencing: applications in medical research.
Genome Med. 2009 Apr 17;1(4):40. doi: 10.1186/gm40.
6
Chromatin maps, histone modifications and leukemia.
Leukemia. 2009 Jul;23(7):1243-51. doi: 10.1038/leu.2009.40. Epub 2009 Mar 26.
7
NA-Seq: a discovery tool for the analysis of chromatin structure and dynamics during differentiation.
Dev Cell. 2009 Mar;16(3):466-81. doi: 10.1016/j.devcel.2009.02.002.
8
ChIP-seq accurately predicts tissue-specific activity of enhancers.
Nature. 2009 Feb 12;457(7231):854-8. doi: 10.1038/nature07730.
9
Transcriptome-guided characterization of genomic rearrangements in a breast cancer cell line.
Proc Natl Acad Sci U S A. 2009 Feb 10;106(6):1886-91. doi: 10.1073/pnas.0812945106. Epub 2009 Jan 30.
10
Transcriptome sequencing to detect gene fusions in cancer.
Nature. 2009 Mar 5;458(7234):97-101. doi: 10.1038/nature07638. Epub 2009 Jan 11.
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