Hello! I am attempting to match the snRNAseq samples to the WGS data. I have found the demultiplexing metadata file and the WGS metadata file which have matching specimen IDs. I haven't been able to find the correct variant calling file with the specimen IDs so I can look at the specific genotypes of that sample. Which variant calling file should I look at specifically that also contains the specimen ID? Thanks in advanced! Alana