Identification of complex genomic rearrangements in cancers using CouGaR

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nFuse: Discovery of complex genomic rearrangements in cancer using high-throughput sequencing

Complex Genomic Rearrangements (CGRs) are emerging as a new feature of cancer genomes. CGRs are characterized by multiple genomic breakpoints, and thus have the potential to simultaneously affect multiple genes, fusing some genes and interrupting other genes. Analysis of high-throughput whole genome shotgun sequencing (WGSS) is beginning to facilitate the discovery and characterization of CGRs,...

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nFuse: Discovery of complex genomic rearrangements in cancer using high-throughput sequencing Supplementary Text

Supplemental nFuse pipeline overview The nFuse method builds upon Comrad (McPherson et al., 2011b), our previous work on rearrangement detection in matched RNA-seq and WGSS. We begin this section by briefly describing Comrad, then describe significant differences between Comrad and nFuse. An overview of the nFuse pipeline is shown in Figure 1.

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Discovery of Complex Genomic Rearrangements in Cancer Using High-Throughput Sequencing

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ژورنال

عنوان ژورنال: Genome Research

سال: 2016

ISSN: 1088-9051,1549-5469

DOI: 10.1101/gr.211201.116