| GetListCountsByDist | R Documentation |
Return, in dataframes via a list, the counts (or proportion) of provided "Positions" by distance from feature positions. If the input list contains 2 GRanges, 2 dataframes ("Position" vs featureStart; "Position" vs featureEnd) will be exported in the output instead of 1 dataframe ("Position" vs featureStart).
GetListCountsByDist( listGRangesDist, lAddCorrectedDistFrom5pTo3p = TRUE, lGetPropInsteadOfCounts = TRUE )
listGRangesDist |
A GRangesList with 1 or 2 GRanges objects containing ranges of given "Positions" with their distance to feature positions. |
lAddCorrectedDistFrom5pTo3p |
If TRUE, the distance will be corrected to reflect 5' to 3' direction and will be stored in a new column (dist_5to3). Defaults to TRUE. |
lGetPropInsteadOfCounts |
If TRUE, return the proportion of given "Positions" near feature position: counts / sum of counts. If listGRangesDist contains 4 GRanges, the proportion of given "Positions" is calculated near both feature positions: counts / (sum of counts near feature1 + sum of counts near feature2). Defaults to TRUE. |
A list with 1 or 2 dataframe(s) containing "Positions" counts by distance to feature positions:
If 1 GRanges are provided in listGRangesDist, 1 dataframe is provided ("Position" vs featureStart).
If 2 GRanges are provided in listGRangesDist, 2 dataframes are provided ("Position" vs featureStart; "Position" vs featureEnd).
If a given "Position" is within nWindowSizeAroundFeaturePos base pairs of x different feature positions: this given "Position" will then reported x times with the distance to each feature position.
# loading genome
myGenome <- Biostrings::readDNAStringSet(system.file(
package = "DNAModAnnot", "extdata",
"ptetraurelia_mac_51_sca171819.fa"
))
# loading annotation
library(rtracklayer)
myAnnotations <- readGFFAsGRanges(system.file(
package = "DNAModAnnot", "extdata",
"ptetraurelia_mac_51_annotation_v2.0_sca171819.gff3"
))
# Preparing a grangesPacBioGFF and a grangesPacBioCSV datasets
myGrangesPacBioGFF <-
ImportPacBioGFF(
cPacBioGFFPath = system.file(
package = "DNAModAnnot", "extdata",
"ptetraurelia.modifications.sca171819.gff"
),
cNameModToExtract = "m6A",
cModNameInOutput = "6mA",
cContigToBeAnalyzed = names(myGenome)
)
myGposPacBioCSV <-
ImportPacBioCSV(
cPacBioCSVPath = system.file(
package = "DNAModAnnot", "extdata",
"ptetraurelia.bases.sca171819.csv"
),
cSelectColumnsToExtract = c(
"refName", "tpl", "strand", "base",
"score", "ipdRatio", "coverage"
),
lKeepExtraColumnsInGPos = TRUE, lSortGPos = TRUE,
cContigToBeAnalyzed = names(myGenome)
)
myGposPacBioCSV <- myGposPacBioCSV[myGposPacBioCSV$base == "A"]
# Retrieve, in a list, dataframes of ModBase counts per Distance values from feature positions
myModDistGRangesList <- GetDistFromFeaturePos(
grangesAnnotations = myAnnotations,
cSelectFeature = "gene",
grangesData = myGrangesPacBioGFF,
lGetGRangesInsteadOfListCounts = TRUE,
cWhichStrandVsFeaturePos = "both", nWindowSizeAroundFeaturePos = 600,
lAddCorrectedDistFrom5pTo3p = TRUE,
cFeaturePosNames = c("TSS", "TTS")
)
myModDistCountsList <- GetListCountsByDist(
listGRangesDist = myModDistGRangesList,
lAddCorrectedDistFrom5pTo3p = TRUE,
lGetPropInsteadOfCounts = TRUE
)
myModDistCountsList
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