Description Usage Arguments Value Examples
View source: R/getLincRNAPvalue.R
Run CNCDriver lincRNA p-value calculation
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22  | getLincRNAPvalue(
  inputFileDir,
  outputFileDir,
  lincRNARegionBedFile,
  elementKeyWord = "lincRNA",
  triNucleotideDistributionFile,
  filterOutBlacklistMutations,
  mutationBlacklistFile,
  replicationTimingGenomeBinnedFile,
  replicationTimingElementBinnedFile,
  tumorType,
  mutationType,
  cellType,
  replicationTimingCutOff,
  seedNum = 42,
  reSampleIterations,
  reRunPvalueCutOff = 0.1,
  useCores,
  taskNum,
  unitSize,
  debugMode = FALSE
)
 | 
inputFileDir | 
 The path for prepared R object file [for example,reducedFunseqOutputNCDS_GBM.Rd]  | 
outputFileDir | 
 The path for output files  | 
lincRNARegionBedFile | 
 The defintion of promoter regions in bed file format  | 
elementKeyWord | 
 Default is "lincRNA", the keyword of lincRNA annotation in FunSeq2  | 
triNucleotideDistributionFile | 
 Cancer type specific mutation counts in 96 trinucleotide category  | 
filterOutBlacklistMutations | 
 TRUE or FALSE  | 
mutationBlacklistFile | 
 The file for mutation blacklist regions  | 
replicationTimingGenomeBinnedFile | 
 Replication timing value at 1MB bin  | 
replicationTimingElementBinnedFile | 
 Replication timing value of each element within 1MB bin  | 
tumorType | 
 Study name  | 
mutationType | 
 User provided mutated gene list  | 
cellType | 
 Cell type of the study, [ BJ, GM12878, HeLaS3, HepG2, IMR90, K562, MCF7, SKNSH or average ]  | 
replicationTimingCutOff | 
 Default is 0.2, a numeric value ranging from 0 to 1  | 
seedNum | 
 User provided random number seed, default is 42  | 
reSampleIterations | 
 User provided re-sapling iteration numbers  | 
reRunPvalueCutOff | 
 Default is 0.1, a numeric value ranging from 0 to 1  | 
useCores | 
 Default is 1, number of cpu to use  | 
taskNum | 
 Default is 0, 0 means to run all elements  | 
unitSize | 
 Number of elements to run per task  | 
debugMode | 
 TRUE or FALSE  | 
results data frame
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15  | #date<-getRunDates(latest=TRUE)
cancerType<-"KIRC"
selectedSampleId<-NA
#worDir<-getwd()
mutSig2CVthreshold<-0.1
rareMutationUpperLimit<-0.3
rareMutationLowerLimit<-0.1
rareMutationFreq<-0.02
#runNetBox2(dataDir,cancerType,
#           mutationList,ampGeneList,delGeneList,epiSilencedList,
#           mutationFreq,ampGeneFreq,delGeneFreq,epiSilencedFreq,
#           pathwayCommonsDb,directed,
#           linkerPValThreshold,communityDetectionMethod,
#           keepIsolatedNodes,verbose=TRUE)
 | 
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