binCoverage | R Documentation |
Example usage for E-M
binCoverage(
bsseq,
bins,
which = NULL,
QDNAseq = TRUE,
readLen = 100,
paired = TRUE
)
bsseq |
A bsseq object - supplied to getCoverage() |
bins |
Bins to summarize over - from tileGenome or QDNAseq.xxYY |
which |
Limit to specific regions? - functions as an import() (DEFAULT: NULL) |
QDNAseq |
Return a QDNAseqReadCounts? - if FALSE, returns a GRanges (DEFAULT: TRUE) |
readLen |
Correction factor for coverage - read length in bp (DEFAULT: 100) |
paired |
Whether the data are from paired-end sequencing (DEFAULT: TRUE) |
NOTE: As of early Sept 2019, QDNAseq did not have hg38 capabilities. If you desire to use the hg38 genome, biscuiteer suggests you use a GRanges object to define your bins.
NOTE: As of late July 2020, biscuiteer has started implemented support for hg38, hg19, mm10, and mm9 for bisulfite-specific features, including adaptive GC-content computation and SV integration for adjusting CNV ends.
Binned read counts
bins <- GRanges(seqnames = rep("chr11",10),
strand = rep("*",10),
ranges = IRanges(start=100000*0:9, width=100000)
)
reg <- GRanges(seqnames = rep("chr11",5),
strand = rep("*",5),
ranges = IRanges(start = c(0,2.8e6,1.17e7,1.38e7,1.69e7),
end= c(2.8e6,1.17e7,1.38e7,1.69e7,2.2e7))
)
orig_bed <- system.file("extdata", "MCF7_Cunha_chr11p15.bed.gz",
package="biscuiteer")
orig_vcf <- system.file("extdata", "MCF7_Cunha_header_only.vcf.gz",
package="biscuiteer")
bisc <- readBiscuit(BEDfile = orig_bed, VCFfile = orig_vcf,
merged = FALSE)
bc <- binCoverage(bsseq = bisc, bins = bins, which = reg, QDNAseq = FALSE)
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