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#$Author: schaid $
#$Date: 2007/02/27 20:15:24 $
#$Header: /projects/genetics/cvs/cvsroot/haplo.stats/R/haplo.em.fitter.q,v 1.5 2007/02/27 20:15:24 schaid Exp $
#$Locker: $
#$Log: haplo.em.fitter.q,v $
#Revision 1.5 2007/02/27 20:15:24 schaid
#control max.haps.limit with checkIntMax (see haplo.em and haplo_em_pin)
#
#Revision 1.4 2004/03/19 15:02:44 sinnwell
#keep PACKAGE in all .C calls, required for R, '...' for Splus
#
#Revision 1.3 2004/03/17 21:06:24 sinnwell
#separate calls for .C( for R and Splus
#
#Revision 1.2 2003/08/26 22:09:38 sinnwell
#added GPL License
#
#Revision 1.1 2003/08/26 21:02:24 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
#
haplo.em.fitter <- function(
n.loci,
n.subject,
weight,
geno.vec,
n.alleles,
max.haps,
max.iter,
loci.insert.order,
min.posterior,
tol,
insert.batch.size,
random.start,
iseed1,
iseed2,
iseed3,
verbose){
converge <- 0
min.prior <- 0.0
n.unique <- 0
lnlike <- 0.0
n.u.hap <- 0
n.hap.pairs <- 0
on.exit(
.C("haplo_free_memory", PACKAGE="haplo.stats")
)
tmp1 <- .C("haplo_em_pin",
n.loci=as.integer(n.loci),
n.subject=as.integer(n.subject),
weight=as.double(weight),
geno.vec=as.integer(geno.vec),
n.alleles = as.integer(n.alleles),
max.haps = as.integer(max.haps),
max.iter=as.integer(max.iter),
loci.insert.order=as.integer(loci.insert.order),
min.prior=as.double(min.prior),
min.posterior=as.double(min.posterior),
tol=as.double(tol),
insert.batch.size=as.integer(insert.batch.size),
converge=as.integer(converge),
lnlike=as.double(lnlike),
n.u.hap=as.integer(n.u.hap),
n.hap.pairs=as.integer(n.hap.pairs),
random.start=as.integer(random.start),
iseed1=as.integer(iseed1),
iseed2=as.integer(iseed2),
iseed3=as.integer(iseed3),
verbose=as.integer(verbose),
PACKAGE="haplo.stats")
tmp2 <- .C("haplo_em_ret_info",
n.u.hap=as.integer(tmp1$n.u.hap),
n.loci=as.integer(tmp1$n.loci),
n.pairs=as.integer(tmp1$n.hap.pairs),
hap.prob=as.double(numeric(tmp1$n.u.hap)),
u.hap=as.integer(numeric(tmp1$n.u.hap*tmp1$n.loci)),
u.hap.code=as.integer(numeric(tmp1$n.u.hap)),
indx.subj=as.integer(numeric(tmp1$n.hap.pairs)),
post=as.double(numeric(tmp1$n.hap.pairs)),
hap1code=as.integer(numeric(tmp1$n.hap.pairs)),
hap2code=as.integer(numeric(tmp1$n.hap.pairs)),
PACKAGE="haplo.stats")
obj <- list(tmp1=tmp1, tmp2=tmp2)
return(obj)
}
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