Open lunky-zao opened 9 months ago
yes. A :The soft will skip non bi-allelic(Singleton/ThreeMulti allelic) site and indel site (For bi-allelic indel, you can modify the "REF ALT" to only one base. see the Perl script at the end of this conversation
I provide a script here that can change bi-allelic indel to SNP, which can be reserved for calculation https://github.com/BGI-shenzhen/LDBlockShow/issues/7
when I use a vcf with structure variation, It's warning skip Indel site, there are total skip Indel sites number is : 618346,after filter Remain SNP Number : 0. Does it mean that VCF files with structural variations cannot be used with this software?