matth...@gmail.com
unread,Sep 21, 2017, 4:06:09 PM9/21/17You do not have permission to delete messages in this group
Sign in to report message
Either email addresses are anonymous for this group or you need the view member email addresses permission to view the original message
to bionet-molbio...@moderators.isc.org
Hi,
We have imported a dataset using lmxll, nnxnp and hkxhk coding into MapQTL and correlated with phenotype. A colleague is trying to identify the genotypes with most effect on phenotype so she can subselect a smaller set of plants for a replicate trial. She has been shown how to identify the variance explained by each allele as mu_AB, mu_AC, mu_BC, mu_BD but how do these codes tie to the original allele coding?
Thanks for any help,
Matt