× Single sample (germline) New Antigen Analysis Read me

Neomachine

Variant calling tools suite

Find germline variants in a single sample that are most likely to cause disease. Please upload single file in vcf format



If the assembly is GRCh37, please select below. Default is GRCh38
4. Specific genes of Interest, if any (optional)
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(c) Gandhi K.,Bhasin M., Winship Cancer Institute, Emory University

Contact us: Gandhi Khanjan