Annotate Variants (WGS)

Using a variant track, annotation track, expression track or statistical comparison track, the Annotate Variants (WGS) ready-to-use workflow runs an internal workflow that adds the following annotations to the track:

Run the Annotate Variants (WGS) workflow

  1. Go to the toolbox and select the Annotate Variants (WGS) workflow here:

            Ready-to-Use Workflows | Whole Genome Sequencing (Image whole_genome_folder_closed_16_n_p) | General Workflows (WGS) (Image general_wgs_wf_closed_16_n_p) | Annotate Variants (WGS) (Image annotate_variants_WGS_16_n_p)

  2. In the first wizard step, select the input variant track, annotation track, expression track or statistical comparison track to annotate (figure 20.2).

    Image annotate_variants_step2_wgs
    Figure 20.2: Select the relevant track to annotate.

  3. In the next dialog, you have to select which data set should be used to annotate variants (figure 20.3).

    Image annotate_variants_step1_wgs
    Figure 20.3: Choose the relevant reference Data Set to annotate.

  4. The only parameter that should be specified by the user is which 1000 Genomes population(s) you want to use (figure 20.4). This can be done using the drop-down list found in this wizard step.

    Image annotate_variants_step3_wgs
    Figure 20.4: Select the relevant 1000 Genomes population(s).

  5. In the last wizard step you can check the selected settings by clicking on the button labeled Preview All Parameters. In the Preview All Parameters wizard you can only check the settings, and if you wish to make changes you have to use the Previous button from the wizard to edit parameters in the relevant windows.

  6. Choose to Save your results and click on the button labeled Finish.

Output from the Annotate Variants (WGS) workflow

The outputs generated are:

  1. Filtered Annotated Variant Track Hold the mouse over one of the variants or right-clicking on the variant. A tooltip will appear with detailed information about the variant.
  2. An Amino Acid Track Shows the consequences of the variants at the amino acid level in the context of the original amino acid sequence. A variant introducing a stop mutation is illustrated with a red amino acid.
  3. Track List Annotated Variants A collection of tracks presented together. Shows the annotated variant track together with the human reference sequence, genes, transcripts, coding regions, and variants detected in dbSNP Common, ClinVar, 1000 Genomes, and PhastCons conservation scores (see figure 20.5).

Image annotate_variants_genomebrowserview_wgs
Figure 20.5: The output from the Annotate Variants ready-to-use workflow is a track list containing individual tracks for all added annotations.

It is possible to add tracks to the Track List by dragging the track directly from the Navigation Area to the Track List view. On the other hand, if you delete the annotated variant track, this track will also disappear from the Track List.

Open the annotated track as a table (see figure 20.6). The table and the Track List are linked; if you click on an entry in the table, this particular position in the genome will automatically be brought into focus in the Track List view.

Image annotate_variants_splitview_wgs
Figure 20.6: The output from the Annotate Variants ready-to-use workflow is a track list linked with the variant table view.

You may be met with a warning as shown in figure 20.7. This is simply a warning telling you that it may take some time to create the table if you are working with tracks containing large amounts of annotations. Please note that in case none of the variants are present in ClinVar or dbSNP Common, the corresponding annotation column headers are missing from the result.

Image warning_annoation_table_wgs
Figure 20.7: Warning that appears when you work with tracks containing many annotations.

Adding information from other sources may help you identify interesting candidate variants for further research. For example, common genetic variants (present in the HapMap database) or variants known to play a role in drug response or other relevant phenotypes (present in the ClinVar database) can easily be identified. Furthermore, variants not found in the ClinVar database can be prioritized based on amino acid changes in case the variant causes changes on the amino acid level.

A high conservation level between different vertebrates or mammals in the region containing the variant can also be used to give a hint about whether a given variant is found in a region with an important functional role. If you would like to use the conservation scores to identify interesting variants, we recommend that variants with a conservation score of more than 0.9 (PhastCons score) are prioritized over variants with lower conservation scores.

It is possible to filter variants based on their annotations. This type of filtering can be facilitated using the table filter found at the top part of the table. If you are performing multiple experiments where you would like to use the exact same filter criteria, you can include in a workflow the Filter on Custom Criteria tool configured with the desired set of criteria.