I have a VCF file to which I would like to add an INFO flag for every record that is present in another (LARGE) VCF file. There are a number of tools to do filtering and another set of tools that will merge INFO fields from one VCF to another, but this isn't exactly what I need (though the latter could be adapted, I suppose).
The use case is that I am trying to do a simple panel-of-normals filter to a set of somatic variants. Should be simple, I know!