Hello everyone,
I would just like your help for confirming some of my conclusions:
1- (IM) as a single-QTL model is conducted using scanone() on after running sim_geno() and calc_genoprob():
cross <- read.cross(cross_file)
cross_sim <- sim_geno(cross)
cross_gen <-calc.genoprob(cross_sim)
IM_scan <- scanone(cross_gen)
IM_scan_perm <- scanone(cross_gen, n.perm = n) #To define threshold
2- Then, in order to conduct a multi-QTL analysis, there are three possible ways (I'm not familiar yet with Bayesian method, so)
- CIM: using cim() function (with or without a prior simulation??)
- MQM: which possesses its own pipeline as I understood
- Perform Two-QTL analysis: scantwo(), use the results to built a model with a formula, and a qtl object: makeqtl(), then use the two objects for fitqtl() and/or? stepwiseqtl().
scantwo(cross_gen)
my_form <- y ~ Q1 + Q2 + Q3....
my_qtl <- makeqtl(cross_gen, c(chromosomes), c(positions))
fitqtl(cross_gen, qtl, my_form, get.ests=T) / stepwiseqtl(cross_gen, qtl, my_form)
I hope my message is clear, I have other detailed questions, but I would like to have a clear global picture first.
Thank you and I appreciate your help
Othmane