Dissecting the genetic basis of comorbid epilepsy phenotypes in neurodevelopmental disorders.
Julie ChowMatthew JensenHajar AminiFarhad HormozdiariOsnat PennSagiv ShifmanSanthosh GirirajanFereydoun HormozdiariPublished in: Genome medicine (2019)
In 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 at https://github.com/jchow32/magi-s .