Singapore Undiagnosed Disease Program: Genomic Analysis aids Diagnosis and Clinical Management.

<bold>Objective: </bold>Use next-generation sequencing (NGS) technology to improve our diagnostic yield in patients with suspected genetic disorders in the Asian setting.<bold>Design: </bold>A diagnostic study conducted between 2014 and 2019 (and ongoing) under the Singapore Undiagnosed Disease Program. Date of last analysis was 1 July 2019.<bold>Setting: </bold>Inpatient and outpatient genetics service at two large academic centres in Singapore.<bold>Patients: </bold>Inclusion criteria: patients suspected of genetic disorders, based on abnormal antenatal ultrasound, multiple congenital anomalies and developmental delay.<bold>Exclusion Criteria: </bold>patients with known genetic disorders, either after clinical assessment or investigations (such as karyotype or chromosomal microarray).<bold>Interventions: </bold>Use of NGS technology-whole exome sequencing (WES) or whole genome sequencing (WGS).<bold>Main Outcome Measures: </bold>(1) Diagnostic yield by sequencing type, (2) diagnostic yield by phenotypical categories, (3) reduction in time to diagnosis and (4) change in clinical outcomes and management.<bold>Results: </bold>We demonstrate a 37.8% diagnostic yield for WES (n=172) and a 33.3% yield for WGS (n=24). The yield was higher when sequencing was conducted on trios (40.2%), as well as for certain phenotypes (neuromuscular, 54%, and skeletal dysplasia, 50%). In addition to aiding genetic counselling in 100% of the families, a positive result led to a change in treatment in 27% of patients.<bold>Conclusion: </bold>Genomic sequencing is an effective method for diagnosing rare disease or previous 'undiagnosed' disease. The clinical utility of WES/WGS is seen in the shortened time to diagnosis and the discovery of novel variants. Additionally, reaching a diagnosis significantly impacts families and leads to alteration in management of these patients. [ABSTRACT FROM AUTHOR]