Version 1.5.2
Date: 2024-09-09
-
Updates
- Updated pre-processing code that pulls in missing pathway annotations (KEGG)
- Data updates
- KEGG - 20240904
- WikiPathways - 20240810 (fixed bug in report display)
- MSigDB (including GO) - v2024.1.Hs
- COMPARTMENTS - 2024-09
- BIOGRID - v4.4.237
- Created a dedicated function
cancer_association_rank()
, which ranks a query gene set according to strength of association (using data from the Open Targets Platform) to a primary tumor type/site.
Version 1.5.1
Date: 2024-08-03
-
Updates
- Minor patch that highlights
quarto
as package dependency in installation instructions
- Minor patch that highlights
Version 1.5.0
- Date: 2024-08-02
Changed
- Data updates
- Open Targets Platform (2024.06)
- WikiPathways (20240710)
- COMPARTMENTS (2024-07)
- KEGG (20240626)
- BioGRID (v4.4.236)
- Upgraded sigven/phenOncoX to v0.7.6
- Functionality
- Cell/tissue-type enrichment is no longer available (TissueEnrich package is deprecated)
- HTML report is now based on the quarto framework rather than RMarkdown
- Many modules are now disabled by default in order to reduce size of HTML report output when running in default mode (primarily a Galaxy consideration)
- Limit protein complexes to those harboring at least two members from the query set
Version 1.4.2
- Date: 2023-08-16
Changed
- Data updates
- WikiPathways (20230810)
- COMPARTMENTS (2023-08)
- KEGG (20230710)
- BioGRID (v4.4.224)
- Open Targets Platform (2023.06)
- Upgraded sigven/phenOncoX to
v0.6.3:
- Experimental Factor Ontology (v3.56.0)
- Human Disease Ontology (2023-07-20)
- A limited set of TCGA amplifications/deletions were erroneously left out in v1.4.1 (gene alias matching) - fixed in v1.4.2
- Functionality
- Updated Citation Note sections in report
- Fixed some typos in the report template
Version 1.4.1
- Date: 2023-06-18
Changed
- Data updates
- TCGA (20220329 - v37.0)
- WikiPathways (20230610)
- CancerMine (v50, 20230301)
- COMPARTMENTS (2023-05)
- KEGG (20230330)
- BioGRID (v4.4.222)
- Open Targets Platform (2023.02)
- Cancer Gene Census (v98)
- Network of Cancer Genes (v7.1)
- MSigDB (v2023.1.Hs)
- Upgraded sigven/phenOncoX to
v0.6.1:
- Experimental Factor Ontology (v3.54.0)
- Human Disease Ontology (2023-05-31)
- Functionality
- Added Citation Note section for each output module - key citations
- Added data licensing terms in Documentation & Settings module
Version 1.4.0
- Date: 2023-02-21
Changed
- Data updates
- TCGA (20221212 - v36.0)
- WikiPathways (20230210)
- CancerMine (20230114)
- COMPARTMENTS (2023-01)
- KEGG (20230101)
- Upgraded sigven/phenOncoX to
v0.5.6:
- Experimental Factor Ontology (v3.50.0)
- Human Disease Ontology (2023-01-31)
- Functionality
-
Loading of databases
- Downloading through Google Drive can somethis cause trouble due to
downloading limitations issued by Google. As an alternative approach,
one can now download datasets using another host (server hosted by the
University of Oslo), through the argument
googledrive = FALSE
inoncoEnrichR::load_db()
- Downloading through Google Drive can somethis cause trouble due to
downloading limitations issued by Google. As an alternative approach,
one can now download datasets using another host (server hosted by the
University of Oslo), through the argument
-
Protein-protein interactions
- Users can opt to show isolated nodes (nodes with no interactions) or
not - logical argument to
onco_enrich()
:ppi_show_isolated_nodes
(default FALSE) - Added protein-protein interaction network based on interactions
found in BioGRID
- Users can set a minimum required threshold for the number of evidence items required for each interaction in BioGRID
- New numerical argument to
onco_enrich()
:ppi_biogrid_min_evidence
- Users can restrict the STRING network to physical
interactions only or an extended network also including indirect (
functional ) interactions - API
network type
- New character argument to
onco_enrich()
:ppi_string_network_type
(physical or functional)
- New character argument to
- Previous argument
ppi_score_threshold
is now namedppi_string_min_score
, with a scale that goes from 0 to 1 (as opposed to 0-1000 in previous versions)
- Users can opt to show isolated nodes (nodes with no interactions) or
not - logical argument to
-
Subcellular compartment annotations
- Now using the regularly updated COMPARTMENTS resource as the underlying source for annotation
- Users can set a minimum confidence score for each target compartment
annotation (range from 3 (least confident) to 5 (most confident)), as
well as the required minimum number of channels ( Knowledge,
Text mining or Experimental) that should support a
given target compartment annotation
- New arguments to
onco_enrich()
:subcellcomp_min_confidence
,subcellcomp_min_channels
- New arguments to
-
Annotation of oncogenic/tumor suppressive roles
- A revised approach to assign roles as proto-oncogenes or tumor suppressors is implemented, in which we assign each role with a confidence level (Moderate/Strong/Very strong) pending upon support in manually curated resources (Network of Cancer Genes (NCG) or Cancer Gene Census (CGC)) or support in the biomedical literature (CancerMine)
-
Cancer driver annotation
- A more conservative approach for driver gene status is implemented: requiring support from at least two distinct resources (Network of Cancer Genes (NCG), Cancer Gene Census, TCGA, IntOGen, or CancerMine)
-
Argument renaming - Renamed arguments to
onco_enrich()
for improved naming consistency:ppi_string_min_score
ppi_string_network_type
ppi_biogrid_min_evidence
ppi_show_drugs
ppi_show_isolated_nodes
regulatory_min_confidence
enrichment_p_value_cutoff
enrichment_q_value_cutoff
enrichment_p_value_adj
enrichment_plot_num_terms
enrichment_simplify_go
enrichment_max_geneset_size
enrichment_min_geneset_size
subcellcomp_min_confidence
subcellcomp_show_cytosol
subcellcomp_min_channels
-
Other
- added oncoEnrichR favicon to output HTML reports
-
Loading of databases
Version 1.3.1
- Date: 2022-09-23
Added
- Data updates:
- CancerMine (20220920 - v48)
- TCGA (20220727 - v34.0)
- WikiPathways (20220910)
- Upgraded sigven/oncoPhenoMap to
v0.4.0:
- Experimental Factor Ontology (v3.46.0)
- Human Disease Ontology (2022-08-29)
- Recurrent somatic variants (SNVs/InDels, as found in TCGA) are
appended to Excel output worksheet, tab
RECURRENT_VARIANTS
Version 1.2.2
- Date: 2022-09-02
Changed
- Now using googledrive as data repository host, due to unstable code using Zenodo
Version 1.2.0
- Date: 2022-06-24
Changed
- Moved to zenodo.org for hosting underlying datasets, accessed with zen4R
- MAF objects (TCGA) no longer loaded from GitHub
- Function
oncoEnrichR::write()
now requires the oncoEnrichR database object (oeDB
) as an argument
Version 1.1.1
- Date: 2022-06-16
Added
- Data updates:
- WikiPathways (20220610)
- Configurations for
onco_enrich()
populated at the end of HTML report
Version 1.1.0
- Date: 2022-06-10
Added
- Data updates:
- CancerMine (v46)
- Open Targets Platform (2022.04)
- WikiPathways (20220510)
- GENCODE (v40)
- CGC (v96)
- TCGA (GDC release 32)
- EFO (v42.0)
- Module that shows the occurrence of protein domains among query set members
- Protein-complex cancer relevance score
- New options
-
ppi_node_shadow
- logical indicating if nodes in the PPI network should carry a shadow or not -
show_domain
- logical indicating if report should add section on protein domain frequencies in query set
-
Version 1.0.9
- Date: 2022-03-31
Added
- Data updates:
- CancerMine (v43)
- Open Targets Platform (2022.02)
- WikiPathways (20220310)
- Project Score (July 2021 release)
- New analysis section: Synthetic lethality - shows how
members of the queryset overlaps with predicted synthetic lethality
interactions (as published by De Kegel et al., Cell Systems, 2021)
- add this section in the output with option
--show_synleth
- add this section in the output with option
Changed
- Option
--show_crispr_lof
renamed to--show_fitness
. Corresponding section in HTML report renamed fromCRISPR/Cas9 loss-of-fitness
toGene fitness scores
. - Renamed sections in HTML report:
-
TCGA co-expression
–>Tumor co-expression
-
TCGA aberration frequency
—>Tumor aberration frequencies
-
TCGA prognostic associations
—>Prognostic associations
-
- Sections that include tabsets are now organized so that the initial active tab always contains data (with the exception of all tabs being empty)
Version 1.0.8
- Date: 2022-02-18
Version 1.0.7
- Date: 2021-11-30
Version 1.0.6
- Date: 2021-10-27
Added
- Data updates
- KEGG (20211013)
- WikiPathways (20211010)
- Open Targets Platform (2021.09)
- EFO (v3.35.0), DiseaseOntology (v2021-10-11)
- TCGA (v30, 2021-09-23)
- Protein complex annotations - additions from Compleat, ComplexPortal, PDB, hu.MAP2
- New functionality
- Report modules
-
Regulatory interactions - (DoRothEA)
- View overlap between members of queryset with previously established regulatory interactions (TF-target relationships) from the DoRothEA resource
-
Ligand-receptor interactions - (CellChatDB)
- Explore potential ligand-receptor interactions in the query set, as found in the CellChat database
-
Regulatory interactions - (DoRothEA)
- Report styling options
- Choose your own Bootswatch theme for HTML report - option
html_report_theme
- Choose where the table of contents are placed in the HTML report
(floating-left or static at the top) - option
html_floating_toc
- Choose your own Bootswatch theme for HTML report - option
- Arguments to
oncoEnichR::onco_enrich()
:-
html_floating_toc
- logical, if set to FALSE, table of contents in HTML report will be placed on top of the main document -
html_report_theme
- character, choose between different Bootswatch themes for style in HTML report -
show_regulatory
- logical, show regulatory interactions module (DoRothEA) -
min_confidence_reg_interaction
- character, minimum confidence of regulatory interactions included from DoRothEA (‘A’,‘B’,‘C’, or ‘D’) -
show_ligand_receptor
- logical, show ligand-receptor interaction module (CellChatDB) -
num_terms_enrichment_plot
- integer, number of enriched Gene Ontology terms (max) to show in enrichment barplots (module Functional Enrichment)
-
- Default gene rankings
- In the modules Regulatory Interactions and Tissue and cell type enrichment, interactions/targets are ranked according to a quantitative cancer association score cancer_max_rank (maximum gene-cancer association rank (Open Targets Platform) across primary sites)
- Report modules