GenVisR-package | GenVisR |
brcaMAF | Truncated BRCA MAF file |
cnFreq | Construct copy-number frequency plot |
cnFreq_buildMain | Construct CN frequency plot |
cnFreq_qual | check input to cnFreq |
cnSpec | Construct copy-number cohort plot |
cnSpec_buildMain | Construct CN cohort plot |
cnSpec_qual | Construct CN cohort plot |
cnView | Construct copy-number single sample plot |
cnView_buildMain | construct CN plot |
cnView_qual | check input to cnView |
compIdent | Construct identity snp comparison plot |
compIdent_bamRcnt | Count nucleotide reads at SNP locations |
compIdent_bamRcnt_qual | Count nucleotide reads at SNP locations |
compIdent_buildMain | Compare sample identities |
compIdent_format | Format readcount tables from compIdent |
covBars | Construct an overall coverage cohort plot |
covBars_buildMain | Construct coverage cohort plot |
covBars_qual | Construct coverage cohort plot |
cytoGeno | Cytogenetic banding dataset |
genCov | Construct a region of interest coverage plot |
genCov_alignPlot | align plots on an axis |
genCov_assign_ggplotGrob_height | assign ggplotGrob height |
genCov_assign_ggplotGrob_width | assign ggplotGrob width |
genCov_buildCov | build coverage plot |
genCov_buildTrack | build label for plot |
genCov_extr_ggplotGrob_height | extract ggplotGrob height |
genCov_extr_ggplotGrob_width | extract ggplotGrob width |
genCov_qual | Perform quality control on genCov data |
genCov_trackViz | Overlay tracks with plots |
geneViz | Construct a gene-features plot |
geneViz_buildGene | build gene plot |
geneViz_calcGC | Calculate GC content |
geneViz_cdsFromTXID | cdsFromTXID |
geneViz_extrCDS | Extract CDS |
geneViz_extrUTR | Extract UTR |
geneViz_formatCDS | format cds |
geneViz_formatUTR | format UTR |
geneViz_Granges2dataframe | Convert Granges object to dataframe |
geneViz_mapCoordSpace | Map regions to transformed space |
geneViz_mapCovCoordSpace | Map coverage track regions to transformed space |
geneViz_mergeRegions | Create Region Table |
geneViz_mergeTypeRegions | Create Typed Region Table |
geneViz_mergeTypes | Merge Typed Region Tables |
GenVisR | GenVisR |
HCC1395_Germline | Germline Calls |
HCC1395_N | Normal BAM |
HCC1395_T | Tumor BAM |
hg19chr | hg19 chromosome boundaries |
ideoView | Construct an ideogram |
ideoView_buildMain | build chromosome |
ideoView_formatCytobands | reformat cytogenetic band data frame |
ideoView_qual | Check input to ideoView |
lohSpec | Plot LOH data |
lohSpec_buildMain | Plot LOH data |
lohSpec_fileGlob | Grab data for lohSpec |
lohSpec_lohCalc | Calculate loh difference |
lohSpec_qual | Check input to lohSpec |
lohSpec_slidingWindow | Obtain LOH data |
lohSpec_stepCalc | Obtain average loh within each step |
lohSpec_tileCalc | Calculate loh difference |
lohSpec_tilePosition | Obtain window information |
lohSpec_tileWindow | Obtain LOH data |
lohSpec_windowPosition | Obtain window information |
lohView | Construct LOH chromosome plot |
lohView_buildMain | construct loh plot |
lohView_qual | check input to lohView |
lolliplot | Construct a lolliplot |
lolliplot_AA2sidechain | Convert AA to side chain classification |
lolliplot_buildMain | Construct Lolliplot |
lolliplot_Codon2AA | Convert Codon to AA |
lolliplot_constructGene | Construct gene information |
lolliplot_DNAconv | Convert DNA character string |
lolliplot_dodgeCoordX | dodge coordinates |
lolliplot_dodgeCoordY | dodge coordinates |
lolliplot_fetchDomain | fetch protein domains |
lolliplot_mutationObs | format mutation observations |
lolliplot_qual | Check input to lolliplot |
lolliplot_reduceLolli | Reduce Lolli |
lolliplot_transcriptID2codingSeq | fetch protein length |
LucCNseg | Truncated CN segments |
multi_align | align CN/LOH plots on x axis |
multi_buildClin | plot clinical information |
multi_chrBound | retrieve and format CN_cohort plot supplemental data |
multi_cytobandRet | Retrieve cytogenetic bands |
multi_selectOut | Choose output |
multi_subsetChr | subset based on chr |
SNPloci | Identity snps |
TvTi | Construct transition-transversion plot |
TvTi_alignPlot | align TvTi plots on y axis |
TvTi_annoTransTranv | Annotate Transitions and Transversions |
TvTi_buildMain | build transitions/transversions |
TvTi_calcTransTranvFreq | Calculate Transition/Transversion Frequency |
TvTi_convMAF | Convert .maf format to internal format |
TvTi_convMaf | Convert .maf format to internal format |
TvTi_qual | Check input to TvTi |
TvTi_rmIndel | Remove indels |
TvTi_rmMnuc | Remove multinucleotide codes |
waterfall | Construct a waterfall plot |
waterfall_align | align plots |
waterfall_buildGenePrevelance | plot mutation recurrence in genes |
waterfall_buildMain | Plot a mutation heatmap |
waterfall_buildMutBurden_A | plot mutation burden |
waterfall_buildMutBurden_B | plot mutation burden |
waterfall_build_proportions | Build mutational profile plot |
waterfall_calcMutFreq | Calculate Synonymous/Nonsynonymous mutation frequency |
waterfall_Custom2anno | Convert Custom File |
waterfall_geneAlt | mutation sample cutoff gene based |
waterfall_geneRecurCutoff | Mutation Recurrence Cutoff |
waterfall_geneSort | sort waterfall file by gene |
waterfall_hierarchyTRV | Hiearchical removal of MAF entries |
waterfall_MAF2anno | Convert MAF File |
waterfall_MGI2anno | Convert MGI File |
waterfall_NA2gene | Assign NA samples a gene |
waterfall_palette_names | waterfall_palette_names |
waterfall_qual | Check input to mutSpec |
waterfall_rmvSilent | Silent Mutation Removal |
waterfall_sampAlt | mutation sample subset sample based |
waterfall_sampSort | sort samples in an internal waterfall file. |
waterfall_select_palette | Helper function to select a colour palette |