- added support for gene-level SCNA data frames to be used as input for
create_features_df()and added an example gene-level SCNA data frameexample_gene_scna_table
- Moved
org.Hs.eg.db,TxDb.Hsapiens.UCSC.hg19.knownGeneandTxDb.Hsapiens.UCSC.hg38.knownGenefrom "Imports" to "Suggests" per new CRAN policy. Relevant functions raise error if the required package is not installed.
- fixed a CRAN error due to a package documentation issue (#7)
- Added GRCh38 support
- Updated the cancer-type-specific thresholds
- Updated citation to the method's article where necessary
- Updated the MTL model after fixing the issue below
- Fixed issue in
MCR_table. The coordinates were converted to hg19 (from hg18)
- Made use of
caret::predict.trainexplicit - Removed 'Homo.sapiens' from Imports field (not used)
- Fixed an issue in
create_SCNA_score_df()where the SCNA score was not calculated because the column name for "MCR_overlap_percent" was incorrectly assigned as "transcript_overlap_percent" - Updated the MTL classification model
TCGA_MTL_fitandspecific_thresholdsafter fixing the issue above
- Updated citation information, correcting author name
- Minor changes in utility functions
- Added the
na.stringargument tocreate_noncoding_impact_score_df(),predict_coding_impact()andcreate_features_df()as the string that was used to indicate when a score is not available during annotation with ANNOVAR (default = ".") - Generalized
determine_hotspot_genes()to able to use occurrence annotations from different versions of COSMIC - Updated all data
Initial release