Closed kriemo closed 1 year ago
it would be useful to have an additional filter to exclude a reporting a 2nd or 3rd variant based on frequency. this would help with recovery of high coverage sites, which often are multiallelic due to sequencing errors.
it would be useful to have an additional filter to exclude a reporting a 2nd or 3rd variant based on frequency. this would help with recovery of high coverage sites, which often are multiallelic due to sequencing errors.