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

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...

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Detalles Bibliográficos
Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7287090/
https://www.ncbi.nlm.nih.gov/pubmed/32522981
http://dx.doi.org/10.1038/s41467-020-16487-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7287090/
https://www.ncbi.nlm.nih.gov/pubmed/32522981
http://dx.doi.org/10.1038/s41467-020-16487-z

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