| refineqtlF | R Documentation |
Extended version of the R/qtl function refineqtl for
function-valued traits. Iteratively scan the positions for QTL in the context of a
multiple QTL model, to try to identify the positions that maximize SLOD
criteria, for a fixed QTL model.
refineqtlF(
cross,
pheno.cols,
usec = c("slod", "mlod"),
qtl,
covar = NULL,
formula,
method = c("hk", "imp"),
verbose = TRUE,
maxit = 10,
incl.markers = TRUE,
keeplodprofile = TRUE
)
cross |
An object of class |
pheno.cols |
Columns in the phenotype matrix to be used as the phenotype. |
usec |
Which method to use ( |
qtl |
A QTL object, as produced by |
covar |
A matrix or data.frame of covariates. These must be strictly numeric. |
formula |
An object of class |
method |
Indicates whether to use multiple imputation or Haley-Knott regression. |
verbose |
If TRUE, give feedback about progress. If |
maxit |
Maximum number of iterations. |
incl.markers |
If FALSE, do calculations only at points on an evenly spaced grid. |
keeplodprofile |
If TRUE, keep the LOD profiles from the last iteration as attributes to the output. |
An object of class "qtl", with QTL placed in their new positions.
Il-Youp Kwak, <email: ikwak2@stat.wisc.edu>
Zeng, Z.-B., Kao, C.-H., and Basten, C. J. (1999) Estimating the genetic architecture of quantitative traits. _Genet. Res._ *74*, 279-289.
Haley, C. S. and Knott, S. A. (1992) A simple regression method for mapping quantitative trait loci in line crosses using flanking markers. _Heredity_ *69*, 315-324.
refineqtl, refineqtlM
data(exd)
exd <- calc.genoprob(exd, step=2)
qtl1.c <- makeqtl(exd, chr = 2, pos = 30, what = "prob")
thisqtl1.c <- refineqtlF(exd, pheno.cols = 1:10, qtl = qtl1.c,
method = "hk")
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