Description Usage Arguments Value
Mostly renamed function names.
cbind_SNPs
has been renamed to cbind_snp_files
.
rowconcatenate
has been renamed to cbind_snp_files
.
imputation_accuracy1
and imputation_accuracy3
has been replaced by imputation_accuracy
.
The difference between the two former functions is now covered by the adaptive
-argument of the latter.
mergeChips
has been renamed to rbind_snp_files
.
phasotogeno
and phasotogeno_int
have been replaced by
convert_phases
.
The difference between the two former functions is covered by the int
argument in the new function.
rbind_SNPs
has been renamed to rbind_snp_files
.
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 | cbind_SNPs(fns, fnout, nlines, ncols, skiplines, excludeids, int)
rowconcatenate(fns, fnout, nlines = NULL, ncols = NULL, skiplines = 0,
excludeids = integer(0))
imputation_accuracy3(truefn, imputefn, nSNPs = NULL, nAnimals = NULL,
NAval = 9, standardized = TRUE)
imputation_accuracy1(truefn, imputefn, nSNPs = NULL, nAnimals = NULL,
NAval = 9, standardized = TRUE)
mergeChips(hdid, ldid, hdpos, ldpos, hdfn, ldfn, fnout, outpos = NULL,
missing = 9)
phasotogeno(phasefn, genofn, ncol = NULL, nrow = NULL)
phasotogeno_int(phasefn, genofn, ncol = NULL, nrow = NULL)
rbind_SNPs(hdid, ldid, hdpos, ldpos, hdfn, ldfn, fnout, outcol = NULL,
na = 9, format = NULL, int = TRUE)
|
fns |
Character vector of filenames to concatenate. Max 255 characters per filename due to R-Fortran. |
fnout |
Filename of resulting file |
nlines |
Number of lines to read from each file. When |
ncols |
Number of columns to read from each file. When |
skiplines |
Integer, number of lines to skip before outputting. |
excludeids |
Integer vector of first column id's to exclude from the output. |
int |
Logical (default |
truefn, imputefn |
Deprected, was filename to files with true and imputed genotype matrix. |
nSNPs |
Deprecated, use |
nAnimals |
Deprecated, use |
NAval |
Deprecated, use |
standardized |
Logical, whether to center and scale genotypes by dataset in |
hdid |
IDs of HD genotyped individuals. Corresponds to (subset of) first column of |
ldid |
IDs of LD genotyped individuals. Corresponds to (subset of) first column of |
hdpos |
Integer vector of where columns in |
ldpos |
Integer vector of where columns in |
hdfn |
Filename of HD genotypes. |
ldfn |
Filename of LD genotypes. |
outpos |
Integer vector of collective SNP positions. Default to sorted, union of |
missing |
Missing value. |
phasefn |
Filename of input file, every two rows are for same animal. |
genofn |
Filename of intended output. |
ncol |
Number of columns to read, if |
nrow |
Number of rows to maximally read from |
outcol |
Integer, number of columns in output file. When |
na |
Value of missing genotypes. |
format |
Character, Fortran edit descriptors for output. See parseformat. |
Number of rows written.
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