I am trying to shift my field from model organisms to human genetics. I have started working on case-control studies using exome sequencing. I have experience in working on NGS and am well versed with its analysis. However, after generating the variants, I don't know how to proceed. So, can the members here give recommendations for any workshops or short courses that could give me an idea of what sort of analyses to perform in case-control studies and also what the relevant tools are for these studies?
Thanks and regards