Hello,
There are two choices in the configuration presents, "DeepVariant" and "DeepVariantWGS", for glnexus_cli (v1.4.1). They have the same description "Joint call DeepVariant whole genome sequencing gVCFs". I wonder if they are the same. Do the presets work for different sequencing data, like NGS (Illumina) data and PacBio data, since both of them can be treated with DeepVariant?
Hello, There are two choices in the configuration presents, "DeepVariant" and "DeepVariantWGS", for glnexus_cli (v1.4.1). They have the same description "Joint call DeepVariant whole genome sequencing gVCFs". I wonder if they are the same. Do the presets work for different sequencing data, like NGS (Illumina) data and PacBio data, since both of them can be treated with DeepVariant?
Thank you very much!