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Lassmann, Timo; Francis, Richard W; Weeks, Alexia; Tang, Dave; Jamieson, Sarra E; Broley, Stephanie; Dawkins, Hugh J S; Dreyer, Lauren; Goldblatt, Jack; Groza, Tudor; Kamien, Benjamin; Kiraly-Borri, Cathy; McKenzie, Fiona; Murphy, Lesley; Pachter, Nicholas; Pathak, Gargi; Poulton, Cathryn; Samanek, Amanda; Skoss, Rachel; Slee, Jennie; Townshend, Sharron; Ward, Michelle; Baynam, Gareth S; Blackwell, Jenefer M
Npj genomic medicine, 12/2020, Volume: 5, Issue: 1Journal Article
Exome sequencing has enabled molecular diagnoses for rare disease patients but often with initial diagnostic rates of ~25-30%. Here we develop a robust computational pipeline to rank variants for reassessment of unsolved rare disease patients. A comprehensive web-based patient report is generated in which all deleterious variants can be filtered by gene, variant characteristics, OMIM disease and Phenolyzer scores, and all are annotated with an ACMG classification and links to ClinVar. The pipeline ranked 21/34 previously diagnosed variants as top, with 26 in total ranked ≤7th, 3 ranked ≥13th; 5 failed the pipeline filters. Pathogenic/likely pathogenic variants by ACMG criteria were identified for 22/145 unsolved cases, and a previously undefined candidate disease variant for 27/145. This open access pipeline supports the partnership between clinical and research laboratories to improve the diagnosis of unsolved exomes. It provides a flexible framework for iterative developments to further improve diagnosis.
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