CoveredLength: Compute the genomic length covered by sequence reads
In benja0x40/Tightrope: ChIP-seq normalization according to background reads density
Description
Usage
Arguments
Value
See Also
View source: R/GenomicRanges.R
Description
Compute the genomic length covered by sequence reads
Usage
1
CoveredLength(cvg)
Arguments
cvg
a coverage object, see GenomicAlignments::coverage.
Value
CoveredLength returns the genomic length covered by sequencing reads.
See Also
GenomicCoverage
benja0x40/Tightrope documentation built on May 24, 2019, 1:35 a.m.
R Package Documentation
Browse R Packages
We want your feedback!
Note that we can't provide technical support on individual packages. You should contact the package authors for that.
Description Usage Arguments Value See Also
View source: R/GenomicRanges.R
Description
Compute the genomic length covered by sequence reads
Usage
1 | CoveredLength(cvg)
|
Arguments
cvg |
a coverage object, see GenomicAlignments::coverage. |
Value
CoveredLength returns the genomic length covered by sequencing reads.
See Also
GenomicCoverage
R Package Documentation
Browse R Packages
We want your feedback!
Note that we can't provide technical support on individual packages. You should contact the package authors for that.
Embedding an R snippet on your website
Add the following code to your website.
For more information on customizing the embed code, read Embedding Snippets.