Closed MartinKahabka closed 3 weeks ago
Save results in tsv file of format: # Information about mutation ChrVariant PosVariant NumberSeverePos NumberSevereNeg NumberNotSeverePos NumberNotSevereNeg IDSeverePos IDSevereNeg IDNotSeverePos IDNotSevereNeg
where ChrVariant/PosVariant correlates to the chromosome the variant is on/the position of the chromosome where the variant is on where Severe/NotSevere correlates with a patient that had severe/not severe symptoms. where Pos/Neg correlates to positive: variant was found/negative: variant was not found where ID correlates to the unique ID of each patient
The result of the runVariantProm.sh safes the lines from the Input-VCF
Now the mutations should be analysed
Desired output: For each mutation, save the patiented ID that have and do not have the given mutation. For each mutation, save the amount of mutations that correspond to "severe" and "not severe" patients