Nothing
#$Author: sinnwell $
#$Date: 2009/04/08 18:40:58 $
#$Header: /projects/genetics/cvs/cvsroot/haplo.stats/R/print.haplo.em.q,v 1.9 2009/04/08 18:40:58 sinnwell Exp $
#$Locker: $
#$Log: print.haplo.em.q,v $
#Revision 1.9 2009/04/08 18:40:58 sinnwell
#*** empty log message ***
#
#Revision 1.8 2009/04/08 17:52:05 sinnwell
#use R's pchisq with lower.tail=FALSE for more signif digits
#
#Revision 1.7 2008/12/12 22:18:43 sinnwell
#return invisible(df)
#
#Revision 1.6 2008/02/11 22:52:27 sinnwell
#edit the message for missing rows
#
#Revision 1.5 2007/11/07 21:03:39 sinnwell
#add digits
#
#Revision 1.4 2004/04/06 20:39:39 sinnwell
#use nlines to limit printouts in vignettes
#
#Revision 1.3 2004/02/26 23:04:28 sinnwell
#print.banner to printBanner
#
#Revision 1.2 2003/08/26 22:09:38 sinnwell
#added GPL License
#
#Revision 1.1 2003/08/26 20:59:40 schaid
#Initial revision
#
# License:
#
# Copyright 2003 Mayo Foundation for Medical Education and Research.
#
# This program is free software; you can redistribute it and/or modify it under the terms of
# the GNU General Public License as published by the Free Software Foundation; either
# version 2 of the License, or (at your option) any later version.
#
# This program is distributed in the hope that it will be useful, but WITHOUT ANY
# WARRANTY; without even the implied warranty of MERCHANTABILITY or
# FITNESS FOR A PARTICULAR PURPOSE. See the GNU General Public License for
# more details.
#
# You should have received a copy of the GNU General Public License along with this
# program; if not, write to the Free Software Foundation, Inc., 59 Temple Place, Suite 330,
# Boston, MA 02111-1307 USA
#
# For other licensing arrangements, please contact Daniel J. Schaid.
#
# Daniel J. Schaid, Ph.D.
# Division of Biostatistics
# Harwick Building Room 775
# Mayo Clinic
# 200 First St., SW
# Rochester, MN 55905
#
# phone: 507-284-0639
# fax: 507-284-9542
# email: schaid@mayo.edu
#
print.haplo.em <- function(x, digits=max(options()$digits-2, 5), nlines=NULL, ...){
printBanner("Haplotypes")
df <- data.frame(x$haplotype,round(x$hap.prob,digits))
names(df) <- c(x$locus.label, "hap.freq")
if(is.null(nlines)) print(df)
else print(df[1:nlines,])
invisible()
if(x$converge==0)
warning("EM failed to converge")
printBanner("Details")
pval <- NA
if(x$df.lr > 0) {
if(is.R()) {
pval = pchisq(x$lr, x$df.lr, lower.tail=FALSE)
} else {
pval = 1-pchisq(x$lr, x$df.lr)
}
}
cat("lnlike = ",round(x$lnlike,digits),"\n")
cat("lr stat for no LD = ",round(x$lr,digits),", df = ",x$df.lr,", p-val = ",round(pval,digits),"\n")
if(length(x$rows.rem > 0)) {
cat("\nResults may be incomplete because one or more subjects was removed\n")
}
invisible(df)
}
Any scripts or data that you put into this service are public.
Add the following code to your website.
For more information on customizing the embed code, read Embedding Snippets.