file.conf to the end of the file.name, right before the disease status (last) column. The output will contain only the patients for which confounding variables exist (other patients will be omitted), so new family file will be written.
pre7.add.conf.var(file.name, dir.file, file.fam, dir.fam = dir.file, file.conf,
dir.conf = dir.file, file.out, fam.out = file.fam, dir.out)file.name can be found.
file.fam can be found.
patientID1 1 2 ...
patientID2 3 1 ...
patientID3 2 2 ...
... - Column 1: patient ID, exactly the same names should appear in
file.fam;
* order does not matter;
* some patients may be missing;
* no new patients should appear in file.conf (if they
don't exist in file.fam)
- Column 2: the confounding variable must have no more than 3
different values.
- Other columns are optional, may be included if there are more
confounding variables (3 categories each)
- No header
- Tab separated
- No missings or NAs
file.conf can be found.
file.name, plus confounding variables, only for the patients mentioned in file.conf.
file.out and fam.out should be saved.
pre6.merge.genos, pre7.add.conf.var.unix,
pre8.split.train.test, pre8.split.train.test.batch
print("See the demo 'gendemo'.")
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