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Dear Chrigi,

GenomeBrowse is for visualization purposes only and does not have functionality for identifying de Novo mutations.

The tutorials available on our website are designed for our analysis software SNP & Variation Suite (SVS). SVS allows you to perform analysis on data in supported formats, to identify de Novo candidates you will minimally need VCF files for your proband and at least one parent.

If you would like to try out SVS for your analysis needs please go to our website at the following link and click the button to request a trial of the software.

http://goldenhelix.com/products/SNP_Variation/index.html

Please let us know how we can help you further.

Thanks, Jami... Golden Helix, Inc.