During the studies, we were given the task of carrying out simple analyzes using simplified vcf files, which only contain chromosome numbers, identification numbers and genotypes; something like that:
Chr1 353 1/1 1/1 0/1 0/1...
Chr1 355 1/1 1/1 0/1 0/1...
and so on...
We were given two files - one with sick animals and one with healthy animals. What kind of comparison, analysis, testing can be done here and some conclusions can be drawn from it? It doesn't have to be anything complicated as this is the first project of its kind and its main goal is to focus on using parallel programming in R.