Description Usage Arguments Value See Also Examples
Takes user provied bed regions, and check for validity of them. Read bam or bed alignment files and convert to 1 nt bed and call detect binding site from 1nt bed.
1 2 3 4 5 6 7 8 9 10 11 12 | DetectBindingSitesBed(
BedFile,
IPfiles,
BackgroundFiles,
genome,
genomeBuild,
DB = "UCSC",
fdrValue = 0.05,
expName = "Motif_Centric_Peaks",
windowSize = 100,
format = ""
)
|
BedFile |
Motif locations in bed format file |
IPfiles |
IP ChIP-seq alignment files |
BackgroundFiles |
Background ChIP-seq alignment files. Can be Input experimetn, DNA whole exctract, etc. |
genome |
The genome name such as "Hsapiens", "Mmusculus", "Dmelanogaster" |
genomeBuild |
The genome build such as "hg38", "hg19", "mm10", "dm3" |
DB |
The database of genome build. default: "UCSC" |
fdrValue |
FDR value cut-off |
expName |
The name of the output table |
windowSize |
Window size around binding site. The total region would be 2*windowSize+1 |
format |
alignment format and should be one of these: "BAMPE", "BAMSE", "BEDPE", "BEDSE" |
peakCallingStatistics A list FRiPs, sequence statistics, and Motif statistics
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 | # FUR candidate motifs in NC_000913 E. coli
FurMotifs=system.file("extdata", "FurMotifs.bed", package="Motif2Site")
# ChIP-seq datasets in bed single end format
IPFe <- c(system.file("extdata", "FUR_fe1.bed", package="Motif2Site"),
system.file("extdata", "FUR_fe2.bed", package="Motif2Site"))
Inputs <- c(system.file("extdata", "Input1.bed", package="Motif2Site"),
system.file("extdata", "Input2.bed", package="Motif2Site"))
FURfeBedInputStats <-
DetectBindingSitesBed(BedFile=FurMotifs,
IPfiles=IPFe,
BackgroundFiles=Inputs,
genome="Ecoli",
genomeBuild="20080805",
DB="NCBI",
expName="FUR_Fe_BedInput",
format="BEDSE"
)
|
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