Hi team, I have a quick question regarding the

phenotype

column in the

samplesheet.csv

for nf-core/raredisease v2.6.0. For example, if the proband (ID = A001) is affected (

phenotype = 2

), and his father (ID = B001) is also affected, should I also set the father’s

phenotype

to 2? I’d like to confirm whether the pipeline assumes that there is only one affected individual per family/trio (i.e., only the proband should have

phenotype = 2

), or if multiple affected individuals within the same family are supported. Many thanks in advance!