Entering edit mode
Antoni Picornell
▴
40
@antoni-picornell-3780
Last seen 10.2 years ago
Hello,
I am trying to impute genomic data in one case-control study with 2000
patients (1000+1000) and Illumina 1M.
I need to perform 2 tasks:
1. Impute missing values in this 1Mx2000 matrix
2. Impute complete genotypes for a list of SNPs that are not in our
platform.
As far as I know, this can be done with non-R programs such as impute,
mach,
beagle or even plink (with poor results in this last case). In R we
have the
package GeneABEL, which could be useful in order to obtain the mach
input from
illumina data.
Does anybody knows if there is some package in R that performs these
kinds of
tasks? How do you deal with this issue (even using non-R programs)?
Thanks,
Antoni Picornell