FindHighFreqCNVs: FindHighFreqCNVs
In mbertalan/iPsychCNV: iPsychCNV
Description
Usage
Arguments
Details
Value
Author(s)
Source
Examples
Description
FindHighFreqCNVs: Identify CNVs with high frequency among the samples.
Usage
1
FindHighFreqCNVs(df, OverlapCutoff = 0.8)
Arguments
Df:
Data frame with predicted CNVs for each sample.
OverlapCutoff:
Unknown, default = 0.8.
Details
Specifically designed to handle noisy data from amplified DNA on phenylketonuria (PKU) cards. The function is a pipeline using many subfunctions.
Value
Data frame with predicted CNVs.
Author(s)
Marcelo Bertalan, Louise K. Hoeffidng.
Source
Examples
1
Unknown.
mbertalan/iPsychCNV documentation built on May 22, 2019, 12:19 p.m.
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Description Usage Arguments Details Value Author(s) Source Examples
Description
FindHighFreqCNVs: Identify CNVs with high frequency among the samples.
Usage
1 | FindHighFreqCNVs(df, OverlapCutoff = 0.8)
|
Arguments
Df: |
Data frame with predicted CNVs for each sample. |
OverlapCutoff: |
Unknown, default = 0.8. |
Details
Specifically designed to handle noisy data from amplified DNA on phenylketonuria (PKU) cards. The function is a pipeline using many subfunctions.
Value
Data frame with predicted CNVs.
Author(s)
Marcelo Bertalan, Louise K. Hoeffidng.
Source
Examples
1 | Unknown.
|
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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