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- W3156278322 abstract "Abstract The integration of viruses into the human genome is known to be associated with tumorigenesis in many cancers, but the accurate detection of integration breakpoints from short read sequencing data is made difficult by human-viral homologies, viral genome heterogeneity, coverage limitations, and other factors. To address this, we present Exogene, a sensitive and efficient workflow for detecting viral integrations from paired-end next generation sequencing data. Exogene’s read filtering and breakpoint detection strategies yield integration coordinates that are highly concordant with those found in long read validation sets. We demonstrate this concordance across 6 TCGA Hepatocellular carcinoma (HCC) tumor samples, identifying integrations of hepatitis B virus that are validated by long reads. Additionally, we applied Exogene to targeted capture data from 426 previously studied HCC samples, achieving 98.9% concordance with existing methods and identifying 238 high-confidence integrations that were not previously reported. Exogene is applicable to multiple types of paired-end sequence data, including genome, exome, RNA-Seq or targeted capture." @default.
- W3156278322 created "2021-04-26" @default.
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- W3156278322 date "2021-04-19" @default.
- W3156278322 modified "2023-09-26" @default.
- W3156278322 title "Exogene: A performant workflow for detecting viral integrations from paired-end next-generation sequencing data" @default.
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- W3156278322 doi "https://doi.org/10.1101/2021.04.19.440427" @default.
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