Description Usage Arguments Value
View source: R/makePythonCommands.R
Create commands to run helper python scripts that automate SNP extraction via PennCNV infer_snp_allele.pl for a cohort.
1 2 3 4 5 6 7 8 9 | makePythonCommands(
penn_path,
pfb_file,
penn_trio_list,
triocnv_file,
n_flanking_snp = 60,
dataset = "TEST",
run_dir
)
|
penn_path |
Full path to PennCNV installation folder |
pfb_file |
Full path to PFB file used in the analysis |
penn_trio_list |
Full path to tab-separated file, listing one trio per line in order father,mother,offspring with full paths to raw data files for each, as used in PennCNV trio |
triocnv_file |
Full path to annotated trio file for offspring (after inheritance map) |
n_flanking_snp |
Integer. A number of probes to extract in upstream and downstream flanks of CNV. Default is 60. |
dataset |
Dataset string used throughout the analysis. Must be consistent. Default is TEST. |
run_dir |
Full path to where extract the snp data. Will be incorporated into extract commands. |
A data table with merged sample and CNV ids as well as original tristates and counts of segments merged
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