Hi,
If I split the VCF file by chromosome number and process each vcf_chr separately through Pangolin, would the results differ compared to running the analysis on the entire VCF file without splitting?
Thank you for your time in clarifying my question.
Hi,
If I split the VCF file by chromosome number and process each vcf_chr separately through Pangolin, would the results differ compared to running the analysis on the entire VCF file without splitting?
Thank you for your time in clarifying my question.