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A: comparing vcf files of disease (affected) and normal (unaffected) samples

Dear friends,

My requirement is to find list of variants which are present in affected but not in unaffected samples, then I have to prepare a list For example,

Samples           4:1243-SNV     5:1277-SNV       15:4070-SNV    ….. ….. …… …… ….. …..      16:5335-SNV 
A(affected)       C_T            A_G              A_T            ….. ….. …… …… ….. …..      A_C
B(unaffected)     C_C            A_A              A_A            ….. ….. …… …… ….. …..      A_A
C(affected)       C_T            A_G              A_T            ….. ….. …… …… ….. …..      A_C
D(affected)       C_T            A_G              A_T           ….. ….. …… …… ….. …..       A_C

Any help friends.

I generated the vcf files using GATK tool.

variant-calling vcf genotype snp

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