Hi,
How do I use tabix to get a single VCF file for multiple SNPs on 1000 genomes (phase 3) data? I'd prefer to use 'rs' IDs instead of genomic locations.
Thanks!
How do I use tabix to get a single VCF file for multiple SNPs on 1000 genomes (phase 3) data? I'd prefer to use 'rs' IDs instead of genomic locations.
Thanks!