Upgrade. Combine predCrossVar with other functions for GS pipeline and add high level wrapping functions that implement/automatic cross predictions, and more.
See predCrossVar, the OG codebase.
[ ] Improve input format for SNP-effects into predictCrosses()
. More flexible SNP-effect list-column naming (instead of opinionated e.g. allelesubeffectlist)? Particularly for the DirDom model.
[ ] Improve phenotype input e.g. for runGenomicPredictions()
and runParentWiseCrossVal()
.
[ ] What would make the package BrAPI compliant?
[ ] SNP marker ID naming conventions are probably too strict; add flexibility / robustness
[ ] More flexibility for the crosses2predict()
function: reciprocal crosses? don't include selfs?
[ ] Change predCrossMeans()
so that it can accept either dosages
or a haploMat
. Currently, predictCrosses()
requires users to supply both dosages
and haploMat
. Changing predCrossMeans()
in this way will allow users of predictCrosses()
to supply only the haploMat
if they are predicting both cross means and variances, or only dosages
if predicting only means.
[ ] modelType="AD_geno"
or something like that --> genotypic additive-dominance partition allowing prediction of $\mu_{TGV}$ in addition to $\mu_{BV}$ but without the genome-wide directional dominance part implemented in modelType="DirDom"
.
[ ] When you set getMarkEffs=TRUE
in runGenomicPredictions()
, tell the user that the function is erroring because they forgot to input the dosage matrix via dosages=
.
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