| triples.posterior {nem} | R Documentation |
Function triples.posterior estimates the hierarchy triple-wise. In each step only a triple of nodes
is involved and no exhaustive enumeration of model space is needed as in function score.
triples.posterior(D, type="mLL",para=NULL, hyperpara=NULL,Pe=NULL,Pmlocal=NULL,Pm=NULL,lambda=0,delta=1, triples.thrsh=.5,verbose=TRUE) ## S3 method for class 'triples': print(x,...)
D |
data matrix. Columns correspond to the nodes in the silencing scheme. Rows are phenotypes. |
type |
see nem |
para |
vector with parameters a and b for "mLL", if count matrices are used |
hyperpara |
vector with hyperparameters a0, b0, a1, b1 for "FULLmLL" |
Pe |
prior position of effect reporters. Default: uniform over nodes in hierarchy |
Pmlocal |
local model prior for the four models tested at each node: a vector of length 4 with positive entries summing to one |
triples.thrsh |
threshold used when combining tripel models for each edge. Default: only edges appearing in more than half of triples are included in the final graph. |
Pm |
prior on model graph (n x n matrix) with entries 0 <= priorPhi[i,j] <= 1 describing the probability of an edge between gene i and gene j. |
lambda |
regularization parameter to incorporate prior assumptions. |
delta |
regularization parameter for automated E-gene subset selection (CONTmLLRatio only) |
verbose |
do you want to see progress statements printed or not? Default: TRUE |
x |
nem object |
... |
other arguments to pass |
triples.posterior is an alternative to exhaustive search
by the function score and more accurate than pairwise.posterior.
For each triple of perturbed genes
it chooses between the 29 possible models. It then uses model averaging to combine the triple-models into a final graph.
print.triples gives an overview over the 'triples' object.
nem object
Florian Markowetz <URL: http://genomics.princeton.edu/~florian>
Markowetz F, Kostka D, Troyanskaya OG, Spang R: Nested effects models for high-dimensional phenotyping screens. Bioinformatics. 2007; 23(13):i305-12.
data("BoutrosRNAi2002")
res <- nem(BoutrosRNAiDiscrete[,9:16],para=c(.13,.05),inference="triples")
# plot graph
plot(res,what="graph")
# plot posterior over effect positions
plot(res,what="pos")
# estimate of effect positions
res$mappos