mTADA is a framework for identifying risk genes from de novo mutations in multiple traits

• Published in: Nature communications Vol. 11; no. 1; p. 2929
• Main Authors: Nguyen, Tan-Hoang, Dobbyn, Amanda, Brown, Ruth C., Riley, Brien P., Buxbaum, Joseph D., Pinto, Dalila, Purcell, Shaun M., Sullivan, Patrick F., He, Xin, Stahl, Eli A.
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 10-06-2020; Nature Publishing Group; Nature Portfolio
• Subjects: 45; 45/23; 45/43; 631/114/2785; 631/208/205; 631/208/366; 631/443/592/2727; Cardiovascular diseases; Coronary artery disease; Disorders; Epilepsy; Exome Sequencing - methods; Genes; Genetic Predisposition to Disease - genetics; Heart diseases; Humanities and Social Sciences; Humans; Intellectual disabilities; Intellectual Disability - genetics; Mental disorders; multidisciplinary; Mutation; Mutation - genetics; Offspring; Risk; Schizophrenia; Science; Science (multidisciplinary); Statistical methods
• ISSN: 2041-1723; 2041-1723
• DOI: 10.1038/s41467-020-16487-z

Joint analysis of multiple traits can result in the identification of associations not found through the analysis of each trait in isolation. Studies of neuropsychiatric disorders and congenital heart disease (CHD) which use de novo mutations (DNMs) from parent-offspring trios have reported multiple putatively causal genes. However, a joint analysis method designed to integrate DNMs from multiple studies has yet to be implemented. We here introduce multiple-trait TADA (mTADA) which jointly analyzes two traits using DNMs from non-overlapping family samples. We first demonstrate that mTADA is able to leverage genetic overlaps to increase the statistical power of risk-gene identification. We then apply mTADA to large datasets of >13,000 trios for five neuropsychiatric disorders and CHD. We report additional risk genes for schizophrenia, epileptic encephalopathies and CHD. We outline some shared and specific biological information of intellectual disability and CHD by conducting systems biology analyses of genes prioritized by mTADA.
Joint analysis of multiple traits can increase power and provide insights into shared genetic architecture. Here, Nguyen et al. develop multi-trait TADA (mTADA), an extension of TADA (transmission and de novo association test) that jointly analyses de novo mutations of traits for improved risk-gene identification power.