Dissecting the genetic basis of comorbid epilepsy phenotypes in neurodevelopmental disorders

ConclusionsIn summary, our method identifies modules enriched with de novo non-synonymous mutations and can capture specific networks that underlie the epilepsy phenotype and display distinct enrichment in relevant biological processes. MAGI-S is available athttps://github.com/jchow32/magi-s.
Source: Genome Medicine - Category: Genetics & Stem Cells Source Type: research