[Genabel-commits] r791 - pkg/GenABEL/R
noreply at r-forge.r-project.org
noreply at r-forge.r-project.org
Sat Oct 8 13:48:15 CEST 2011
Author: lckarssen
Date: 2011-10-08 13:48:15 +0200 (Sat, 08 Oct 2011)
New Revision: 791
Modified:
pkg/GenABEL/R/polygenic.R
Log:
In GenABEL's polygenic(): Fixed minor typos in the documentation. Also slightly rewrote the remark that polygenic_hglm() is faster than polygenic(), because that is no longer the case since GenABEl v1.6-8.
Modified: pkg/GenABEL/R/polygenic.R
===================================================================
--- pkg/GenABEL/R/polygenic.R 2011-09-30 10:53:56 UTC (rev 790)
+++ pkg/GenABEL/R/polygenic.R 2011-10-08 11:48:15 UTC (rev 791)
@@ -82,7 +82,7 @@
#' @param patchBasedOnFGLS if FGLS checks not passed, 'patch' fixed
#' effect estimates based on FGLS expectation
#' @param llfun function to compute likelihood (default 'polylik_eigen', also
-#' avalable -- but not recommeneded -- 'polylik')
+#' available -- but not recommended -- 'polylik')
#' @param ... Optional arguments to be passed to \code{\link{nlm}} or (\code{\link{optim}})
#' minimisation function
#'
@@ -128,16 +128,17 @@
#' @author Yurii Aulchenko, Gulnara Svischeva
#'
#' @note
-#' Presence of twins may complicate your analysis. Check kinship matrix for
+#' Presence of twins may complicate your analysis. Check the kinship matrix for
#' singularities, or rather use \code{\link{check.marker}} for identification
#' of twin samples. Take special care in interpretation.
#'
-#' If a trait (no covarites) is used, make sure that order of IDs in
+#' If a trait (no covarites) is used, make sure that the order of IDs in the
#' kinship.matrix is exactly the same as in the outcome
#'
#' Please note that there is alternative to 'polygenic',
#' \code{\link{polygenic_hglm}}, which is faster than
-#' 'polygenic'.
+#' polygenic() with the llfun='polylik' option, but slightly slower than the
+#' default polygenic().
#'
#' @seealso
#' \code{\link{polygenic_hglm}},
@@ -148,7 +149,7 @@
#' # note that procedure runs on CLEAN data
#' data(ge03d2ex.clean)
#' gkin <- ibs(ge03d2ex.clean,w="freq")
-#' h2ht <- polygenic(height ~ sex + age,kin=gkin,ge03d2ex.clean)
+#' h2ht <- polygenic(height ~ sex + age, kin=gkin, ge03d2ex.clean)
#' # estimate of heritability
#' h2ht$esth2
#' # other parameters
@@ -158,8 +159,8 @@
#' # twice maximum log-likelihood
#' -h2ht$h2an$minimum
#'
-#' #for binary trait (experimental)
-#' h2dm <- polygenic(dm2 ~ sex + age,kin=gkin,ge03d2ex.clean,trait="binomial")
+#' # for binary trait (experimental)
+#' h2dm <- polygenic(dm2 ~ sex + age, kin=gkin, ge03d2ex.clean, trait="binomial")
#' # estimated parameters
#' h2dm$h2an
#'
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