Conrad.hg19.common.CNVs: Conrad et al common CNVs
In drramki-chop/edm: Scalable workflow to identify copy Number variants from exome sequencing data
Description
Usage
Format
Source
Description
Positions of common CNV calls (detected in a panel of 42 sample) from
the Conrad et al paper (Nature 2010). This is build hg19 of the human
genome.
Usage
1
data(Conrad.hg19)
Format
A data frame with common CNV calls.
Source
Conrad et al, Origins and functional impact of copy number variation
in the human genome, Nature 2010
drramki-chop/edm documentation built on June 6, 2020, 8:48 a.m.
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Description Usage Format Source
Description
Positions of common CNV calls (detected in a panel of 42 sample) from the Conrad et al paper (Nature 2010). This is build hg19 of the human genome.
Usage
1 | data(Conrad.hg19)
|
Format
A data frame with common CNV calls.
Source
Conrad et al, Origins and functional impact of copy number variation in the human genome, Nature 2010
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.
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