improved functions to call copy number states from bulk DNA or Integer Copy Number
calls can be exported as text (deletion, loss, gain, amplification) or with cbioportal notation, -2, -1, 0, +1, +2
calls include an additional category representing > 20 copies of a gene. Term is high_amplification, and in cbioportal is labeled as +4
added functions to estimate alteration frequencies in bulk DNA or Integer Copy Number
added option to plot bins or gene alteration frequences
minor changes for compatibility
simplified create_chromosome_annotation base functions
add_in_silico_root
now exits if "X" contains cell.name
e.g. 'diploid'
adds plot_sK to inspect kParameter and kStable
new method for assigning clusters in Bray Curtis Dissimilarity
added function to add an in-silico root cell and clone
bin.id checks between chrmoInfo and gene.index
standardizing function names, renamed as export_cnr and summary_cnr
pull_gene_details now pulls information from a gene list, rather than regions
added functions to order bins and genes, and are implemented by default in sync_cnr
added default colors to vdjHeatmap
modified names of functions related to gene and region information lookup
getting_started vignette cleanup
copynumbers example data now matches that of the example cnr
new sync_cnr function to resyncronize cnr tables after merge, etc This is now applied by default after running addCells, addPheno, and buildCNR
adding default colors to heatmap plots
debuged DDRC.g creation as there was a bug introduced and went missing
added function to append information to the gene.index
removing color map objects
split_cnr
function to convert a cnr object into a list of cnr split by a categorical variable
e.g. sample ID, treated vs control, etc.added option to change gene.type column in genotype_vdj
changed seqnames
column to chrom
in gene index and matches chromInfo
debugged other functions after setting gene.type.column
cnr now uses default bioMart gene_biotype
column name
introduction of gene lookup functions based on coordinates
further debugging to pass CRAN
added functions to associate copy number to categorical phenotypes
added functions to pull copy number froms specific genes
added functions to visualize association resutls, e.g. manhattan plots, and effect plots
added functions to convert from .seg Run Length Encoding (RLE) data to bin coordinates
added functions to facilitate creating chromsome annotations for custom plots
other helper functions
removed @export tag in DepMap, OncoKB, and GISTIC2 specific functions
tagged internal functions
use of vegan::diversity rather than entropy::entropy
roundCNR
arguments from buildCNR
added clone assignment ranked by FGA and/or frequency
added ability to root the cell phylogenetic tree
added function to run clone phylogenetic analysis
added VDJ clustering with Bray-Curtis Dissimilarity
fixed vdj cell type in keepCells and excludeCells
added support for subbsetting based on bins, genes, full chromosomes and genomic coordinates
debugged build notes 0 errors ✔ | 0 warnings ✔ | 0 notes ✔
added plot_frequencies to plot amplification and deletion frequencies
in setBrayClusters, if tree.height is NULL, the minimum intersect between one-cell and multi-cell clusters is used by default as the tree.height
section on preparing your data added to getting_started.Rmd
minor debugging on warnings, and unit tests
moved badge to maturing
Added summaryCNR function
debugged warnings and notes
Added VDJ genotyping and visualization
Progress status in consensusClusterCNR
Added estimation of alteration frequencies at gene and bin level
Deduplicated example bin to gene tracks
Added DATASET.R to show how example data is generated
Added chromosome tickmarks in HeatmapCNR
Added support for consensus clustering
Added support for K Spectral to select max number of stable clusters from consensus clustering
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