This public repository contains the research and analysis code that was used to generate the results presented in the publication "Genomic basis for RNA alterations in cancer."
The code is organized across several directoris:
event_callingThe scripts used to call the alternative splicing events from aligned RNA-Seq dataexonizationsCode related to detecting exonization events from the splicing graph datafilter_eventsCode filtering for potentially functional events (used for gene centric analysis)gene_centric_tablesCode summarizing the alternative splicing events of all samples into a splice-outlier tableicgc_anno,icgc_colors,icgc_utilsHelper and utility code to take care of logistics and metadatajunction_dbScripts to collect all aligned splice junctions into a joint databasepca_tsneScripts using dimensionality reduction for visualizationstats_eventsCode summarizing the event statisticsutilsUtility and helper functions