Farrel Buchinsky wrote:
I am using dgc.genetics to perform TDT analysis on SNP data from a cohort of
trios.
I now have a file with about 6008 variables. The first few variables related
to the pedigree data such as the pedigree ID the person ID etc. Thereafter
each variable is a specific
On 5/3/06, Uwe Ligges [EMAIL PROTECTED] wrote:
Looks like you have to be much more specific:
tdt() is a function within dgc.genetics.
dgc.genetics is a package written by David Clayton and available at
http://www-gene.cimr.cam.ac.uk/clayton/software/
It consists of extensions to the genetics
Farrel Buchinsky wrote:
On 5/3/06, Uwe Ligges [EMAIL PROTECTED] wrote:
Looks like you have to be much more specific:
tdt() is a function within dgc.genetics.
dgc.genetics is a package written by David Clayton and available at
http://www-gene.cimr.cam.ac.uk/clayton/software/
It
Uwe Ligges ligges at statistik.uni-dortmund.de writes:
The same way. lapply() and sapply() should work for almost all functions
given, if nothing strange happens with environemnts, which is the case here:
The problem is tdt() itself. Note that it has its argument data set to
I am using dgc.genetics to perform TDT analysis on SNP data from a cohort of
trios.
I now have a file with about 6008 variables. The first few variables related
to the pedigree data such as the pedigree ID the person ID etc. Thereafter
each variable is a specific locus or marker. The
I am using dgc.genetics to perform TDT analysis on SNP data from a cohort of
trios.
I now have a file with about 6008 variables. The first few variables related
to the pedigree data such as the pedigree ID the person ID etc. Thereafter
each variable is a specific locus or marker. The variables
