Chr2.phased: Phased Cattle Genotypes from Chromosome 2
In optiSel: Optimum Contribution Selection and Population Genetics
Chr2.phased R Documentation
Phased Cattle Genotypes from Chromosome 2
Description
Phased genotypes from Chromosome 2 (only the first part of the chromosome). Further information on these animals is included in data frame Cattle.
Format
All functions reading phased genotype data assume that the files are in the following format:
Each file has a header and no row names. Cells are separated by blank spaces. The number of rows is equal to the number of markers from the respective chromosome and the markers are in the same order as in the map. There can be some extra columns on the left hand side containing no genotype data. The remaining columns contain genotypes of individuals written as two alleles separated by a character, e.g. A/B, 0/1, A|B, A B, or 0 1. The same two symbols must be used for all markers. Column names are the IDs of the individuals. If the blank space is used as separator then the ID of each individual should be repeated in the header to get a regular delimited file. The columns to be skipped and the individual IDs must have no white spaces.
Use function read.indiv to extract the IDs of the individuals from a genotype file.
Examples
GTfile <- system.file("extdata/Chr2.phased", package="optiSel")
file.show(GTfile)
GT <- read.table(GTfile, header=TRUE, skip=2, check.names=FALSE)
GT[1:10,1:5]
optiSel documentation built on Sept. 11, 2024, 7:19 p.m.
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| Chr2.phased | R Documentation |
Phased Cattle Genotypes from Chromosome 2
Description
Phased genotypes from Chromosome 2 (only the first part of the chromosome). Further information on these animals is included in data frame Cattle.
Format
All functions reading phased genotype data assume that the files are in the following format:
Each file has a header and no row names. Cells are separated by blank spaces. The number of rows is equal to the number of markers from the respective chromosome and the markers are in the same order as in the map. There can be some extra columns on the left hand side containing no genotype data. The remaining columns contain genotypes of individuals written as two alleles separated by a character, e.g. A/B, 0/1, A|B, A B, or 0 1. The same two symbols must be used for all markers. Column names are the IDs of the individuals. If the blank space is used as separator then the ID of each individual should be repeated in the header to get a regular delimited file. The columns to be skipped and the individual IDs must have no white spaces.
Use function read.indiv to extract the IDs of the individuals from a genotype file.
Examples
GTfile <- system.file("extdata/Chr2.phased", package="optiSel")
file.show(GTfile)
GT <- read.table(GTfile, header=TRUE, skip=2, check.names=FALSE)
GT[1:10,1:5]
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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