Pangolin provides both maximum scores and minimum scores. However, determining the cutoff value is crucial. We need to establish the specific values that indicate the significance of a splice variant for our purposes. Since I'm conducting whole genome sequencing (WGS), filtering out numerous variants is necessary. Could you guide me on where to find the cutoff scores?
Pangolin provides both maximum scores and minimum scores. However, determining the cutoff value is crucial. We need to establish the specific values that indicate the significance of a splice variant for our purposes. Since I'm conducting whole genome sequencing (WGS), filtering out numerous variants is necessary. Could you guide me on where to find the cutoff scores?