cnvAggCall: Aggregate CN-state calls from different widths to single call
In daynefiler/mcCNV: Call copy number variants from whole exome/whole genome sequencing data
Description
Usage
Arguments
Details
Description
Aggregate CN-state calls from different widths to single call
Usage
1
cnvAggCall(calls)
Arguments
dat
the input data, see details
Details
Need to add
C1 – TRUE if any interval of the given width that overlaps the exon was
called a CNV
daynefiler/mcCNV documentation built on Dec. 15, 2021, 3:58 a.m.
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Description Usage Arguments Details
Description
Aggregate CN-state calls from different widths to single call
Usage
1 | cnvAggCall(calls)
|
Arguments
dat |
the input data, see details |
Details
Need to add
C1 – TRUE if any interval of the given width that overlaps the exon was called a CNV
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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