Figure 1
From: A community-based resource for automatic exome variant-calling and annotation in Mendelian disorders
Website interface.Screenshots of the relevant sections of the web interface and outline of the user experience. The analysis is submitted through the Create New section, where the user submit the required analysis details. The user can choose to submit a single sample or multiple samples of related individuals and an auto-completion feature helps the user in assigning the correct disease id to the analysis. The user can follow the progress of the analysis in the Analysis section where he will also find a link to the Results page after the analysis is completed.