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VARIFANT

NGS SOFTWARE

VARIANT TOOL

FOR PRACTICAL HANDLING OF NGS DATA

Remember to ctrl-click on app to open the first time

FILTER

 

Quickly remove low quality variants, variants outside of targeted or non-coding region or common in the population

PLOT & REPORT

 

Get a unique feeling of your data by the built-in plotting and reporting tools.

ANNOTATE

 

Find associations in the literature, previous status as somatic mutations and informations on the possible casual contributions in a practical manner

A GREAT WAY TO ANALYSE

YOUR RESEARCH SEQUENCING DATA

Need assistance with the bioinformatics? Or implementing VARIFANT in your research?

Contact us for an advice or project inquiry

BIOINFORMATICS

SERVICES

No need for bioinformatics skills

Plug and play solutions

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?

Get your FASTQ processed

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.

Copyright @ All Rights Reserved

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)