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Showing 1 to 1 of 1 for “"long-read whole genome sequencing"”.
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Computational methods for the detection of somatic structural variants in cancer genomes using long-read sequencing
… method for the analysis of somatic SVs using long-read whole genome sequencing data from tumours and matched normal samples. SAVANA employs machine learning to distinguish true somatic SVs from germline events and noise. Additionally, I establish best practices for benchmarking SV detection …