Open WouterSteyaert opened 2 months ago
OK. I spotted the problem. my VCF starts with some 'unconventional chromosome' not starting with 'chr' and thus the function 'get_prefix' results in an empty prefix causing the issues. I will filter the VCF beforehand and let you know the result
Dear Jonathan,
When I try running unfazed I always get the notion that there are no usable informative sites, for any input variant. I am wondering if genomes are supported for which the chromosome names start with 'chr', because in the screenoutput it says that there are no intervals for 1:16080000-16090000 (for example) while all my input files are 'chr' based. Do you have an idea why that is?
Best wishes, Wouter