Which function, method and model to use depends on the crosses grown and on the question asked. This vignette gives a decision table and shows how to check that a data set has the crosses an analysis needs.
2 Decision table
Crosses grown
Question
Function
parents, \(F_1\) and reciprocals
combining ability, reciprocal effects
Griffing(Method = 1)
parents and one set of \(F_1\)
combining ability
Griffing(Method = 2)
\(F_1\) and reciprocals, no parents
combining ability, reciprocal effects
Griffing(Method = 3)
one set of \(F_1\) only
combining ability
Griffing(Method = 4)
parents, \(F_1\) and reciprocals
gene action: additive and dominance components, \(W_r\)-\(V_r\) graph
Hayman()
parents, \(F_1\) and reciprocals
maternal and non-maternal reciprocal effects
Griffing(Method = 1, Reciprocal = "split")
a published table of cross means
combining ability from the means and the published error
GriffingMeans()
any of Griffing’s layouts in several environments
stability of gca and sca: interactions with environments
GriffingEnv()
parents and crosses (a check variety optional)
heterosis over the mid-parent, better parent, check
Heterosis()
parents and one set of \(F_1\)
variety effects and average, variety and specific heterosis
GardnerEberhart()
two groups of parents crossed with each other
combining ability of each group
PartialDiallel()
lines crossed with testers
combining ability, contributions of lines and testers
LineTester()
North Carolina Design I, II or III
additive and dominance variance
NCDesign()
not yet grown
number of replicates for the tests
DiallelPower(), DiallelSim()
Model. Choose Model 1 (fixed effects) when the parents are of interest in themselves (the usual case in a breeding programme): it gives effects and standard errors. Choose Model 2 (random effects) when the parents are a random sample of a population and the aim is to estimate variance components (additive and dominance variance).
With \(P\) parents: Method 1 needs \(P\) selfs and \(P(P-1)\) crosses, Method 2 \(P\) selfs and \(P(P-1)/2\) crosses (either way round), Method 3 \(P(P-1)\) crosses and no selfs, Method 4 \(P(P-1)/2\) crosses and no selfs.
4 What happens when a plot or a cross is missing
A missing plot is allowed in Griffing(), GriffingEnv(), Heterosis(), GardnerEberhart(), LineTester() and NCDesign(): the cross means are then least-squares means adjusted for blocks, the number of replicates is the harmonic mean of the plot numbers, and the label of the result says so. Hayman() and PartialDiallel() need every plot. Every cross of the method must be present, though; a missing cross is reported with its name:
[1] "Griffing(): 1 cross(es) of Method 1 are missing from `data` (for example 1 x 2). The analysis needs every cross; for incomplete diallels fit a linear mixed model."
Incomplete diallels need a linear mixed model with the gca, sca and reciprocal effects as random terms.
5 Column names
The arguments take a column by name, as a string, or a vector:
d <- GriffingData1names(d) <-c("Female", "Male", "Block", "GrainYield")fit <-Griffing(y ="GrainYield" , Rep = Block , Cross1 = Female , Cross2 = Male , data = d , Method =1 , Model =1 , Reciprocal =c("combined", "split")[1] )fit$ANOVA
The crosses grown fix the analysis and the method; the purpose fixes the model. Check the cells before the analysis; every analysis reports what is missing.
7 References
Griffing, B. (1956). Concept of general and specific combining ability in relation to diallel crossing systems. Australian Journal of Biological Sciences, 9(4), 463–493.
Hayman, B. I. (1954). The theory and analysis of diallel crosses. Genetics, 39(6), 789–809.
Hayman, B. I. (1954). The analysis of variance of diallel tables. Biometrics, 10(2), 235–244.