Additional file 11 of Structural variant analysis of a cancer reference cell line sample using multiple sequencing technologies
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Additional file 11: Supplementary Table S10. Pathogenic SVs. The annotation of the high confidence SV call set used the AnnotSV software to rank the pathogenic scores. We selected SVs annotated with score of 4 and 5 as well as SVs overlap the genes in Catalogue Of Somatic Mutations In Cancer (COSMIC) database.
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figshare
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2024-08-13
