Hello sir, actually I am having SNP data in hapmap format generated by GBS (crop=maize), I converted the hap to .ped and .map format. the ped form as usually has six column with missing FID,parents, SEX, phenotype. In these regard when I tried calculate allele frequency on chromosome wise, the out put says scanning 0 of 0 chr. (maize chr no is 10)
ex:
ERROR: Problem with MAP file line:
1 S1523360 0 523360
Here the phenotyping data is taken from field for quantitative traits, how can go for case/control for data as there is no controls. suggest me the input format or command line for this situation
Your reply could help me a lot