Fig. 2

Workflow schematic for the Lift and Merge submodule. VCF data files from independent datasets with genomic positions that reflect either the Homo sapiens GRCh37 or GRCh38 genome reference assemblies can be merged. This depicted workflow is specifically for a final merged VCF file configured to have genomic positions in GRCh38. The orange denoted pathway represents GRCh37 data input and the blue denoted pathway represents GRCh38 data input