simuleBasicGenoChr: simuleBasicGenoChr
In belleau/simAnc: What the Package Does (One Line, Title Case)
Usage
Arguments
Value
Author(s)
Examples
View source: R/simGenotypeChr.R
Usage
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simuleBasicGenoChr(
genotype,
infoSNV,
mysegs,
nbSim,
minCov = 10,
seqError = 0.001/3,
dProp = NA
)
Arguments
genotype
data.frame
fileList
a list of GRanges, the segments from multiple
files.
snv
a data.frame
Value
a
Author(s)
Pascal Belleau, Astrid Deschenes
Examples
1
# TODO
belleau/simAnc documentation built on June 11, 2021, 9:09 p.m.
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Usage Arguments Value Author(s) Examples
View source: R/simGenotypeChr.R
Usage
1 2 3 4 5 6 7 8 9 | simuleBasicGenoChr(
genotype,
infoSNV,
mysegs,
nbSim,
minCov = 10,
seqError = 0.001/3,
dProp = NA
)
|
Arguments
genotype |
|
fileList |
a |
snv |
a |
Value
a
Author(s)
Pascal Belleau, Astrid Deschenes
Examples
1 | # TODO
|
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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