Hi!
I am performing variant calling and annotation of some cancer samples.
For the moment, I am checking manually the variants with an entry in the COSMIC database and then going to the COSMIC database website to retrieve information associated to that variant.
I am wondering if there is any way to do this automatically. This is, finding a variant, filtering the ones that have COSMIC annotation, and then having relevant information associated to that variant being retrieved and written to a report (for example).
I see that COSMIC has downloadable data available but still I do now know how to create a relationship between my vcfs and those files.
I know this might be a very broad and dumb question but I am starting my bioinfo path, I would appreciate any hints to the right answer so I can start figuring out by myself.
Thanks!!
Hi, I think others can easily help you with a real example. So give a real and detailed example of expected inputs and outputs.