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v1.1.3
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@abyssum abyssum released this 20 May 11:57
· 15 commits to master since this release
1.1.3
5979208

  • NeoFuse can now accept VCF or tab-separated files with coordinates of structural variants found using whole-genome sequencing data, with the flag "-v". These coordinates serve to increase sensitivity towards weakly expressed fusions and to eliminate fusions with low confidence. (for more information please refer to arriba documentation).

  • Flag "-S" can now be used with NeoFuse to determine how far a genomic breakpoint may be away from a transcriptomic breakpoint to still consider it as a related event. For events inside genes, the distance is added to the end of the gene; for intergenic events, the distance threshold is applied as-is. (Used with "-v" argument. Default: 100000).

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