init_report | R Documentation |
Function that initiates oncoEnrichR report structure
init_report(
oeDB,
project_title = "_Project title_",
project_owner = "_Project owner_",
html_floating_toc = T,
html_report_theme = "default",
query_id_type = "symbol",
ignore_id_err = TRUE,
project_description = "_Project description_",
ppi_string_min_score = 0.9,
ppi_string_network_type = "functional",
ppi_biogrid_min_evidence = 3,
ppi_add_nodes = 30,
ppi_show_isolated_nodes = FALSE,
ppi_node_shadow = TRUE,
ppi_show_drugs = T,
bgset_description = "All annotated protein-coding genes",
bgset_id_type = "symbol",
enrichment_p_value_cutoff = 0.05,
enrichment_p_value_adj = "BH",
enrichment_q_value_cutoff = 0.2,
enrichment_min_geneset_size = 10,
enrichment_max_geneset_size = 500,
enrichment_plot_num_terms = 20,
enrichment_simplify_go = F,
subcellcomp_min_confidence = 3,
subcellcomp_min_channels = 1,
subcellcomp_show_cytosol = F,
regulatory_min_confidence = "D",
fitness_max_score = -2,
show_ppi = T,
show_disease = T,
show_top_diseases_only = T,
show_cancer_hallmarks = T,
show_drug = T,
show_enrichment = T,
show_aberration = T,
show_coexpression = T,
show_subcell_comp = T,
show_fitness = T,
show_cell_tissue = F,
show_ligand_receptor = T,
show_regulatory = T,
show_unknown_function = T,
show_prognostic = T,
show_synleth = T,
show_complex = T,
show_domain = T
)
oeDB |
oncoEnrichR annotation database object |
project_title |
project title (title of report) |
project_owner |
name of project owner |
html_floating_toc |
logical - float the table of contents to the left of the main document content. The floating table of contents will always be visible even when the document is scrolled |
html_report_theme |
Bootswatch theme for HTML report (any of "bootstrap","cerulean","cosmo","default","flatly","journal","lumen","paper","sandstone","simplex","spacelab","united","yeti") |
query_id_type |
character indicating source of query (one of "uniprot_acc", "symbol", "entrezgene", or "ensembl_gene","ensembl_mrna","refseq_mrna","ensembl_protein","refseq_protein") |
ignore_id_err |
logical indicating if analysis should continue when uknown query identifiers are encountered |
project_description |
project background information |
ppi_string_min_score |
minimum score (between 0 and 1) for confidence of retrieved protein-protein interactions (STRING) |
ppi_string_network_type |
STRING network type ('physical' or 'functional') |
ppi_biogrid_min_evidence |
minimum number of evidence items for protein-protein interactions shown (BIOGRID) |
ppi_add_nodes |
number of nodes to add to target set when computing the protein-protein interaction network (STRING/BIOGRID) |
ppi_show_isolated_nodes |
logical indicating if targets/nodes without any interactions should be displayed in the protein-protein interaction network |
ppi_node_shadow |
show shadow for nodes in the displayed PPI network (STRING/BIOGRID) |
ppi_show_drugs |
logical indicating if targeted drugs (> phase 3) should be displayed in protein-protein interaction network |
bgset_description |
character indicating type of background (e.g. "All lipid-binding proteins (n = 200)") |
bgset_id_type |
character indicating source of query (one of "uniprot_acc", "symbol", "entrezgene", or "ensembl_gene","ensembl_mrna","refseq_mrna","ensembl_protein","refseq_protein") |
enrichment_p_value_cutoff |
cutoff p-value for enrichment/over-representation analysis |
enrichment_p_value_adj |
one of "holm", "hochberg", "hommel", "bonferroni", "BH", "BY", "fdr", "none" |
enrichment_q_value_cutoff |
cutoff q-value for enrichment analysis |
enrichment_min_geneset_size |
minimal size of geneset annotated by term for testing in enrichment/over-representation analysis |
enrichment_max_geneset_size |
maximal size of geneset annotated by term for testing in enrichment/over-representation analysis |
enrichment_plot_num_terms |
number of top enriched Gene Ontology terms (max) to show in enrichment barplot |
enrichment_simplify_go |
remove highly similar GO terms in results from GO enrichment/over-representation analysis |
subcellcomp_min_confidence |
minimun confidence level for subcellular compartment annotation in COMPARTMENTS (min = 3, max = 5) |
subcellcomp_min_channels |
minimum number of channels that support a subcellular annotation in COMPARTMENTS |
subcellcomp_show_cytosol |
logical indicating if subcellular heatmap should highlight cytosol as a subcellular protein location or not |
regulatory_min_confidence |
minimum confidence level for regulatory interactions (TF-target) retrieved from DoRothEA ('A','B','C', or 'D') |
fitness_max_score |
maximum loss-of-fitness score (scaled Bayes factor from BAGEL) for genes retrieved from Project Score |
show_ppi |
logical indicating if report should contain protein-protein interaction data (STRING) |
show_disease |
logical indicating if report should contain disease associations (Open Targets Platform, association_score >= 0.05, support from at least two data types) |
show_top_diseases_only |
logical indicating if report should contain top (n = 20) disease associations only pr. query gene (Open Targets Platform) |
show_cancer_hallmarks |
logical indicating if report should contain annotations/evidence of cancer hallmarks per query gene (COSMIC/Open Targets Platform) |
show_drug |
logical indicating if report should contain targeted cancer drug information |
show_enrichment |
logical indicating if report should contain functional enrichment/over-representation analysis (MSigDB, GO, KEGG, REACTOME, NetPath, WikiPathways) |
show_aberration |
logical indicating if report should contain TCGA aberration plots (amplifications/deletions) |
show_coexpression |
logical indicating if report should contain TCGA co-expression data (RNAseq) of query set with oncogenes/tumor suppressor genes |
show_subcell_comp |
logical indicating if report should provide subcellular compartment annotations (COMPARTMENTS) |
show_fitness |
logical indicating if report should provide fitness scores and target priority scores from CRISPR/Cas9 loss-of-fitness screens (Project Score) |
show_cell_tissue |
logical indicating if report should contain tissue-specificity and single cell-type specificity assessments (Human Protein Atlas) of target genes, using data from the Human Protein Atlas |
show_ligand_receptor |
logical indicating if report should contain ligand-receptor interactions (CellChatDB) |
show_regulatory |
logical indicating if report should contain data on transcription factor (TF) - target interactions relevant for the query set (DoRothEA) |
show_unknown_function |
logical indicating if report should highlight target genes with unknown or poorly defined functions (GO/Uniprot KB/NCBI) |
show_prognostic |
logical indicating if mRNA-based (single-gene) prognostic associations to cancer types should be listed (Human Protein Atlas/TCGA) |
show_synleth |
logical indicating if report should list overlap with predicted synthetic lethality interactions (gene paralogs only, De Kegel et al., Cell Systems, 2021) |
show_complex |
logical indicating if report should provide target memberships in known protein complexes (ComplexPortal/Compleat/PDB/CORUM) |
show_domain |
logical indicating if report should provide target memberships in known protein domains (Pfam) |
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