How to run the Identify Rare Disease Causing Mutations in a Family of Four (WES) workflow

This section recapitulates the steps you need to take to start the workflow, each item corresponding to a different wizard windows. For more information on the specific tools used in this workflow, see Hereditary Disease.

To run the Identify Rare Disease Causing Mutations in a Family of Four (WES) workflow, go to:

        Toolbox | Ready-to-Use Workflows | Whole Exome Sequencing (Image exome_sequencing_closed_16_n_p) | Hereditary Disease (Image hereditary_folder_closed_16_n_p) | Identify Rare Disease Causing Mutations in a Family of Four (WGS (Image rare_disease_muta_four_wgs_16_h_p)

  1. Double-click on the Identify Rare Disease Causing Mutations in a Family of Four (WES) tool to start the analysis. If you are connected to a server, you will first be asked where you would like to run the analysis.

  2. Select the targeted region file (figure 14.68).

    The targeted region file is a file that specifies which regions have been sequenced, when working with whole exome sequencing or targeted amplicon sequencing data. This file is something that you must provide yourself, as this file depends on the technology used for sequencing. You can obtain the targeted regions file from the vendor of your targeted sequencing reagents.

    Image targetedregions_ird4_wes
    Figure 14.68: Select the targeted region file you used for sequencing.

  3. Select the sequencing reads from the unaffected sibling (figure 14.69).

    The sequencing reads from the different family members are specified one at a time in the appropriate window. The panel in the left side of the wizard shows the kind of input that should be provided. Select by double-clicking on the reads file name or click once on the file and then on the arrow pointing to the right side in the middle of the wizard.

    Image reads_ird4_wes
    Figure 14.69: Specify the sequencing reads for the appropriate family member.

  4. Select the sequencing reads from for the affected child.
  5. Select the sequencing reads from the mother.
  6. Select the sequencing reads from the father.

  7. Specify the affected child's gender (figure 14.70).

    Image gender_ird4_wes
    Figure 14.70: Specify the proband's gender.

  8. Specify the Hapmap populations that should be used for filtering out variants found in Hapmap for the mother (figure 14.71).

    This can be done using the drop-down list found in this wizard step. Please note that the populations available from the drop-down list can be specified with the Data Management (Image search_database_16_h_p) function found in the top right corner of the Workbench (see Download and configure reference data).

    Image removehapmap_ird4wes
    Figure 14.71: Select the relevant Hapmap population(s).

  9. Specify the Hapmap populations that should be used for filtering out variants found in Hapmap for the father.
  10. Specify the Hapmap populations that should be used for filtering out variants found in Hapmap from the de novo assembly.

  11. Specify the parameters for the Fixed Ploidy Variant Detection tool for the affected child (figure 14.72).

    The parameters used by the Fixed Ploidy Variant Detection tool can be adjusted. We have optimized the parameters to the individual analyses, but you may want to tweak some of the parameters to fit your particular sequencing data. A good starting point could be to run an analysis with the default settings.

    Image fp_settings_ird4_wes
    Figure 14.72: Specify the parameters for the Fixed Ploidy Variant Detection tool.

    The parameters that can be set are:

    • Required variant probability is the minimum probability value of the 'variant site' required for the variant to be called. Note that it is not the minimum value of the probability of the individual variant. For the Fixed Ploidy Variant detector, if a variant site - and not the variant itself - passes the variant probability threshold, then the variant with the highest probability at that site will be reported even if the probability of that particular variant might be less than the threshold. For example if the required variant probability is set to 0.9 then the individual probability of the variant called might be less than 0.9 as long as the probability of the entire variant site is greater than 0.9.
    • Ignore broken pairs: When ticked, reads from broken pairs are ignored. Broken pairs may arise for a number of reasons, one being erroneous mapping of the reads. In general, variants based on broken pair reads are likely to be less reliable, so ignoring them may reduce the number of spurious variants called. However, broken pairs may also arise for biological reasons (e.g. due to structural variants) and if they are ignored some true variants may go undetected. Please note that ignored broken pair reads will not be considered for any non-specific match filters.
    • Minimum coverage: Only variants in regions covered by at least this many reads are called.
    • Minimum count: Only variants that are present in at least this many reads are called.
    • Minimum frequency: Only variants that are present at least at the specified frequency (calculated as 'count'/'coverage') are called.

    For more information about the tool, see http://clcsupport.com/biomedicalgenomicsworkbench/current/index.php?manual=Fixed_Ploidy_Variant_Detection.html.

  12. Specify the parameters for the Fixed Ploidy Variant Detection tool for the father.
  13. Specify the parameters for the Fixed Ploidy Variant Detection tool for the sibling.
  14. Specify the parameters for the Fixed Ploidy Variant Detection tool for the mother.

  15. Specify the parameters for the QC for Target Sequencing tool for the father (figure 14.73).

    When working with targeted data (WES or TAS data), quality checks for the targeted sequencing is included in the workflows. Again, you can choose to use the default settings, or you can choose to adjust the parameters.

    Image qc_settings_ird4_wes
    Figure 14.73: Specify the parameters for the QC for Target Sequencing tool.

    The parameters that can be set are:

    • Minimum coverage provides the length of each target region that has at least this coverage.
    • Ignore non-specific matches: reads that are non-specifically mapped will be ignored.
    • Ignore broken pairs: reads that belong to broken pairs will be ignored.

  16. Specify the parameters for the QC for Target Sequencing tool for the mother.
  17. Specify the parameters for the QC for Target Sequencing tool for the sibling.
  18. Specify the parameters for the QC for Target Sequencing tool for the affected child.

  19. Pressing the button Preview All Parameters allows you to preview all parameters. At this step you can only view the parameters and it is not possible to make any changes. Choose to save the results and click on the button labeled Finish.