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#$Author: sinnwell $
#$Date: 2005/03/30 16:40:22 $
#$Header: /projects/genetics/cvs/cvsroot/haplo.stats/R/print.haplo.score.merge.q,v 1.10 2005/03/30 16:40:22 sinnwell Exp $
#$Locker: $
#$Log: print.haplo.score.merge.q,v $
#Revision 1.10 2005/03/30 16:40:22 sinnwell
#remove banner.width from printBanner
#
#Revision 1.9 2004/04/07 14:08:59 sinnwell
#use nlines for quick print
#
#Revision 1.8 2004/02/26 23:07:36 sinnwell
#print.banner to printBanner
#
#Revision 1.7 2003/10/03 19:32:38 sinnwell
#fix for R release, handles match.call different
#
#Revision 1.6 2003/08/26 16:37:57 sinnwell
#change license
#
#Revision 1.5 2003/06/19 22:05:04 sinnwell
#re-assign row numbers
#
#Revision 1.4 2003/06/19 13:46:02 sinnwell
#add order.by and all.haps options. default is order by score and all.haps=F
#
#Revision 1.3 2003/04/15 18:40:24 sinnwell
#fix merge.bin to x
#
#Revision 1.2 2003/03/06 22:08:40 sinnwell
#insert license, and change getting n.loci
#
#Revision 1.1 2003/01/17 16:29:47 sinnwell
#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.score.merge <- function(x, order.by="score", all.haps=FALSE, digits=max(options()$digits-2, 5), nlines=NULL, ...)
{
### Print haplo.score.merge object to screen
if (!inherits(x, 'haplo.score.merge'))
stop("Not an object of class haplo.score.merge!")
m.call <- match.call()
noOrder <- is.na(pmatch("order.by", names(m.call)))
noAll.haps <- is.na(pmatch("all.haps", names(m.call)))
noDigits <- is.na(pmatch("digits", names(m.call)))
if (!noOrder)
order.by <- m.call[[3]]
if (!noAll.haps) {
if(!noOrder)
all.haps <- m.call[[4]]
else all.haps <- m.call[[3]]
}
# if(length(m.call[[3]])) order.by <- m.call[[3]]
# if(length(m.call[[4]])) all.haps <- m.call[[4]]
n.loci <- (1:length(names(x)))[names(x)=="Hap-Score"] - 1
order.vec <- c("score","freq","haplotype")
order.int <- pmatch(order.by, order.vec)
if(all(is.na(order.int))) order.int <- 1
order.by <- order.vec[order.int]
#if all.haps not requested, then subset to only those w/ a score
if(!all.haps) x <- x[1:length(na.omit(x$"Hap-Score")),]
# Combine haplotypes and results
# round numeric columns to set length digits
df.print <- data.frame(x[,1:n.loci],
round(x[,(n.loci+1):ncol(x)],digits))
# select between 3 different orderings
switch(order.by,
score = {
ord <- 1:nrow(x)
},
freq = {
ord <- (1:nrow(x))[order(x$"Hap-Freq")]
},
haplotype = {
ord <- as.numeric(attributes(haplo.hash(df.print[,1:n.loci])$hap.mtx)$row.names)
})
cat("\n\n")
printBanner("Haplotype Scores, p-values, and Frequencies By Group", border = "-")
df.print <- data.frame(df.print[ord,], row.names=NULL)
if(is.null(nlines))
print(df.print, digits=digits, ...)
else print(df.print[1:nlines,], digits=digits, ...)
invisible()
}
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