Hello,

I have a F1 progeny from two outbred parents (4way cross then) with no missing genotype information and with around 600 markers. R propose 4 methods for interval mapping (em, imp, haley-knott and extended haley-knott)

I wanted to know if I should do the QTL detection with the EM method proposed in R or if another method would fit better than this one for my case. I thought about the multiple imputation method but as I don't have missing genotype data so I am not sure I need it.

Furthermore, i would like to perform after that a QTL detection with Multiple QTL Mapping and i read that "multiple imputation (imp method) has greatest value for the fit and exploration of MQM models". So I am a little lost in the choice of the method for the first step of my qtl detection. Could you give any advice according your experience ?

Thanks

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