Update of package name from “domino2” to “dominoSignal”
Bioconductor Standards
Update to Vignettes presenting application of the DominoSignal pipeline on data formatted as a SingleCellExperiment object
Implemented caching of example data by BiocCache to meet package size limits
Removal of depreciated scripts for running SCENIC. Tutorials for running SCENIC are still present in vignettes
Corrected BiocCheck notes pertaining to coding practices including paste in conditional statements, functions with dontrun examples, usage of seq_len or seq_along in place of seq, and usage of vapply in place of sapply
dominoSignal v0.99.1
Update to Bioconductor version numbering conventions for package submission
dominoSignal v0.2.2
Linkage functions
Addition of new class to summarize linkages in objects
Addition of helper functions to count linkages and compare between objects
Plotting function for differential linkages
Package structure
Adjustments made to meet BioConductor standards
dominoSignal v0.2.1
Updates to domino object construction
Uniform formats for inputs of receptor-ligand interaction databases, transcription factor activity features, and regulon gene lists for operability with alternative databases and transcription factor activation inference methods
Helper functions for reformatting pySCENIC outputs and CellPhoneDB database files to domino-readable uniform formats
Assessment of transcription factor linkage with receptors that function as a heteromeric complex based on correlation between transcription factor activity and all receptor component genes
Assessment of complex ligand expression as the mean of component gene expression for plotting functions
Minimum threshold for the percentage of cells in a cluster expressing a receptor gene for the receptor to be called active within the cluster
Additional linkage slots for active receptors in each cluster, transcription factor-receptor linkages for each cluster, and incoming ligands for active receptors on each cluster
Plotting functions
Chord plot of ligand expression targeting a specified receptor where chord widths correspond to the quantity of ligand expression by each cell cluster
Signaling networks showing only outgoing signaling from specified cell clusters
Gene networks between two cell clusters
Bugfixes
Added host option for gene ortholog conversions using biomaRt for access to maintained mirrors
Transcription factor-target linkages are now properly stored so that receptors in a transcription factor’s regulon are excluded from linkage
Ligand nodes sizes in gene networks correspond to quantity of ligand expression
