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Ryan E. Mills et al.
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inGAP: an integrated next-generation genome analysis pipeline
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SVDetect: a tool to identify genomic structural variations from paired-end and mate-pair sequencing data
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SLOPE: a quick and accurate method for locating non-SNP structural variation from targeted next-generation sequence data
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Suzanne Sindi et al.
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Pindel: a pattern growth approach to detect break points of large deletions and medium sized insertions from paired-end short reads
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Fast and accurate short read alignment with Burrows-Wheeler transform
Heng Li 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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Mapping and sequencing of structural variation from eight human genomes (Reprinted from Nature, vol 453, pg 56-64, 2008)
Jeffrey M. Kidd et al.
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MoDIL: detecting small indels from clone-end sequencing with mixtures of distributions
Seunghak Lee et al.
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Computational methods for discovering structural variation with next-generation sequencing
Paul Medvedev 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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PEMer: a computational framework with simulation-based error models for inferring genomic structural variants from massive paired-end sequencing data
Jan O. Korbel et al.
GENOME BIOLOGY (2009)
Accurate whole human genome sequencing using reversible terminator chemistry
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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Integrated detection and population-genetic analysis of SNPs and copy number variation
Steven A. McCarroll et al.
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Paired-end mapping reveals extensive structural variation in the human genome
Jan O. Korbel et al.
SCIENCE (2007)
Structural variation in the human genome
L Feuk et al.
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E Tuzun et al.
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