Additional file 9 of Structural variant analysis of a cancer reference cell line sample using multiple sequencing technologies
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Additional file 9: Supplementary Table S9. SVs Validated by RNA-seq. For fusion detection from RNA-seq data, we used Star Fusion and Arriba to produce a set of fusion candidates. Gene-fusion events found in the two tools were used to compare with the consensus SV call set to find overlap genes to produce the final integrated SV-Fusion gene call set.
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figshare
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2024-08-13
