Closed BRLIA closed 2 years ago
The output VCF is based on the VCFv4.3 format, so if VG reads that then it should work. However, I am not sure whether VG handles all the different types of genomic differences that SyRI identifies (for ex: translocations or HDRs) . So, you might need to filter it out. This question is probably better suited for the VG developers.
OK,I will try it. Thank you for your help
Hi, I'm going to construct graph genome by VG, and I want to use the SVs detected by SyRI, but I don't know if the VCF file that SyRI output can support it. Thanks