2021 Preprint
M-DATA: A Statistical Approach to Jointly Analyzing De Novo Mutations for Multiple Traits
Abstract: Recent studies have demonstrated that multiple early-onset diseases have shared risk genes, based on findings from de novo mutations (DMNs). Therefore, we may leverage information from one trait to improve statistical power to identify genes for another trait. However, there are few methods that can jointly analyze DNMs from multiple traits. In this study, we develop a framework called M-DATA (Multi-trait framework for De novo mutation Association Test with Annotations) to increase the statistical power of ass…
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“…Alternative methods are needed to quantify concordance of association signals for rare and de novo variants between traits [24]. With shared genetics between traits, we can leverage this to better identify disease genes [25,26].…”
Section: Pleiotropymentioning
confidence: 99%
“…Alternative methods are needed to quantify concordance of association signals for rare and de novo variants between traits [24]. With shared genetics between traits, we can leverage this to better identify disease genes [25,26].…”
Section: Pleiotropymentioning
confidence: 99%
