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_calling
The scripts used to call the alternative splicing events from aligned RNA-Seq dataexonizations
Code related to detecting exonization events from the splicing graph datafilter_events
Code filtering for potentially functional events (used for gene centric analysis)gene_centric_tables
Code summarizing the alternative splicing events of all samples into a splice-outlier tableicgc_anno
,icgc_colors
,icgc_utils
Helper and utility code to take care of logistics and metadatajunction_db
Scripts to collect all aligned splice junctions into a joint databasepca_tsne
Scripts using dimensionality reduction for visualizationstats_events
Code summarizing the event statisticsutils
Utility and helper functions