Entering edit mode
23 months ago
elielsonveloso
•
0
Hello, Biostars community!
I am currently working on a dataset of ~550 SNPs sequenced for 40 patients. My doubt is if it is possible to do genotypic imputation using a single merged VCF containing all The variants for my 40 patients (even if I need to split that merged VCF by chromossome) . I also have Map and Ped files generated by PLINK. My goal is to make all my patients have genotypic data for all the ~550 SNPs .Could anyone help me with that issue? I would appreciate if somente could give me a clue on that!
Thanks in Advance!
