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GeneBe Hub

Overview​

This functionality is not yet publicly available.

In GeneBe you can upload your FASTQ files or your VCF files to analyze them interactively. Filter annotated variants to create a report you can download. Easy as a pie.

The way you work with results in GeneBe mimicks a natural best practice flow.

  1. Browse the full variants lists, apply filters to select variants of interest. Do a quick search to find what is the most interesting. Mark variants that are interesting. After this step you should have some variants selected, with brief hipothesis. Variants marked will appear in your Notebook.
  2. After the first step go to your Notebook. Here you have your variants selected. Now work with them, check every variant carefully, read the literature, check the samples where you previously had these variants, compare the phenotype and finally apply the Tier, add comments.
  3. Variants from the Tier 1 and 2 will automatically go to the Report. In the Report view you can add comments that will be included in the Report and finally: generate the Report based on the Template you've provided, with your organization logo in the header and selected variants in the list or a table.