A streamlined method for detecting structural variants in cancer genomes by short read paired-end sequencing
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A streamlined method for detecting structural variants in cancer genomes by short read paired-end sequencing
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(P356) |
10.1371/JOURNAL.PONE.0048314
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(P698) |
23144753
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(P819) |
2012PLoSO...748314M
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(P932) |
3483208
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(P5875) |
233396882
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