cnv.snap: Apply NLP to genomic reports to extract copy number variants...
In TheMillerLab/genetex: BodyMapR
Description
Usage
Arguments
Value
Description
'cnv.snap()' provides natural language processing tools to abstract copy number variants data SNaPshot reports
Usage
1
Arguments
data
The data frame of the genomic report of interest. This can be copied to the Clipboard from the EHR report by "selecting all" and then "copy". That is the default. If you don't use the clipboard function, you can use a data frame of the text file. The single column data frame should be labeled "Results". Required.
Value
a data frame with two columns: variables (the redcap variable names) and results (the data to be imported in to redcap)
TheMillerLab/genetex documentation built on Dec. 18, 2021, 4:09 p.m.
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Description Usage Arguments Value
Description
'cnv.snap()' provides natural language processing tools to abstract copy number variants data SNaPshot reports
Usage
1 |
Arguments
data |
The data frame of the genomic report of interest. This can be copied to the Clipboard from the EHR report by "selecting all" and then "copy". That is the default. If you don't use the clipboard function, you can use a data frame of the text file. The single column data frame should be labeled "Results". Required. |
Value
a data frame with two columns: variables (the redcap variable names) and results (the data to be imported in to redcap)
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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