Table 1.
A summary of XGR characteristics for tasks achieved and runtime required
Functions | Tasks achieved | Runtimea |
---|---|---|
Enrichment analysis | ||
xEnricher | A template for enrichment analysis | ~40 |
xEnricherGenes | Gene-based enrichment analysis using a wide variety of ontologiesb | ~40 |
xEnricherSNPs | SNP-based enrichment analysis using Experimental Factor Ontology on GWAS traits | ~70 |
xEnricherYours | Custom-based enrichment analysis using user-defined ontologies | ~5 |
xEnrichConciser | Removing redundant ones from enrichment outputs | ~15 |
xEnrichBarplot | Barplot of enrichment outputs | <1 |
xEnrichCompare | Side-by-side barplots of comparative enrichment outputs | <1 |
xEnrichDAGplot | DAG plot of enrichment outputs | <1 |
xEnrichDAGplotAdv | DAG plot of comparative enrichment outputs | <1 |
Annotation analysis | ||
xGRviaGeneAnno | Annotation analysis using nearby gene annotations by a wide variety of ontologiesb | ~60 |
xGRviaGenomicAnno | Annotation analysis using a wide variety of genomic annotationsc | ~30 |
Similarity analysis | ||
xSocialiser | A template for similarity analysis | ~60 |
xSocialiserGenes | Gene-based similarity analysis using structured ontologies on functions, diseases, and phenotypes | ~70 |
xSocialiserSNPs | SNP-based similarity analysis using Experimental Factor Ontology on GWAS traits | ~60 |
xCircos | Circos plot of similarity outputs | ~10 |
xSocialiserDAGplot | DAG plot of one set of terms used for similarity analysis | <1 |
xSocialiserDAGplotAdv | DAG plot of two sets of terms used for similarity analysis | <1 |
Network analysis | ||
xSubneterGenes | Gene-based network analysis | ~60 |
xSubneterSNPs | SNP-based network analysis | ~60 |
xVisNet | Network visualisation | <1 |
aRuntime (measured by seconds) tested using one core on Mac OS X
bIncluding structured ontologies on functions, diseases, and phenotypes, and non-structured ontologies on pathways, regulatory/expression signatures, druggability, structural domains, GTEx eGene tissues, others
cIncluding genomic annotations sourced from ENCODE, FANTOME5, BLUEPRINT Epigenome, Roadmap Epigenomics, The Cancer Genome Atlas, UCSC, others