Remember to ctrl-click on app to open the first time
No need for bioinformatics skills
The VariFant software is developed with the molecular biologist in mind. No hard core bioinformatics skills are required to start the analysis of cancer variants. All you need is a list of variants (VCF or CSV-files) and your research approach.
Problems with variant calling?
Outsource your exome sequencing variant calling: We provide alignment and variant calling from whole exome sequencing and targeted panel sequencing. This enables you to focus on your variants and stop worrying about the initial bioinformatics pipeline. The resulting variants can be opened in VariFant.
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DIURS Engineering & Design
Hoffmannsvej 22 ST TH, 8220 Brabrand, Denmark
The software is developed in collaboration with Aarhus University Hospital and Odense University Hospital, DK.
Part of the work has kindly been supported by Eva & Henry Frænkel Foundation (Eva og Henry Frænkels Mindefond, DK)