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Support for VCF files was added with version 1.1.0 of GenomeBrowse. Single sample VCFs, multi-sample VCFs and even "site"-based VCFs with no sample data are now supported. SNVs and InDels are supported and we will do our best to draw Structural Variants, but their representation in VCF format is less standardized.

We incorporated a new rendering mode for multi-sample "Variant Maps", as well as auto-compression/indexing of VCF to Bgzip/Tabix format required to read files directly for rendering.

Currently any VCF file loaded into GenomeBrowse must be sorted.

Please update to the most recent version of GenomeBrowse to access all available features. To update GenomeBrowse please download the installer from our website.