Additional file 12 of Structural variant analysis of a cancer reference cell line sample using multiple sequencing technologies
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Additional file 12: Supplementary Table S11. SVs Overlap Cancer Genes. High confidence consensus call set SVs were annotated using AnnotSV software. The significant structure variants were compared with the Cancer Gene Census Project of the COSMIC database (GRCh38 COSMIC v90) to find genes are overlapping with the Cancer Gene Census list.
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figshare
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2024-08-13
