相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。Estimation of rearrangement phylogeny for cancer genomes
Chris D. Greenman et al.
GENOME RESEARCH (2012)
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CELL (2011)
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Max A. Alekseyev et al.
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Seungtai Yoon et al.
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Combinatorial algorithms for structural variation detection in high-throughput sequenced genomes
Fereydoun Hormozdiari et al.
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Elaine R. Mardis et al.
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Maximum Likelihood Genome Assembly
Paul Medvedev et al.
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High-resolution mapping of copy-number alterations with massively parallel sequencing
Derek Y. Chiang et al.
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BreakDancer: an algorithm for high-resolution mapping of genomic structural variation
Ken Chen et al.
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Angela A. Steinhardt et al.
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David R. Bentley et al.
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Identification of somatically acquired rearrangements in cancer using genome-wide massively parallel paired-end sequencing
Peter J. Campbell et al.
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A sequence-based survey of the complex structural organization of tumor genomes
Benjamin J. Raphael et al.
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Jan O. Korbel et al.
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Patterns of somatic mutation in human cancer genomes
Christopher Greenman et al.
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E Tuzun et al.
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P Kauraniemi et al.
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De novo repeat classification and fragment assembly
PA Pevzner et al.
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Reconstructing tumor amplisomes
Benjamin J. Raphael et al.
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Reconstructing tumor genome architectures
Benjamin J. Raphael et al.
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DG Albertson et al.
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S Volik et al.
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PA Pevzner et al.
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