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Whole-genome sequencing and data analysis
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Whole-genome sequencing of lysed single cells and bulk samples, and data analyses including somatic coding and noncoding SNV detection, somatic CNV detection, single-cell classification, detection of HBV integration sites, phylogenetic tree construction, and cancer driver gene prediction were detailed in Supplementary information, Data S1.
Copyright and License information: ©2018 Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences
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