set.default.parameters(Sgenes, ...)
mLL
or FULLmLL
or CONTmLL
or CONTmLLBayes
or CONTmLLMAP
or depn
. CONTmLLDens
and CONTmLLRatio
are identical to CONTmLLBayes
and CONTmLLMAP
and are still supported for compatibility reasons. mLL
and FULLmLL
are used for binary data (see BoutrosRNAiDiscrete
) and CONTmLL
for a matrix of effect probabilities. CONTmLLBayes
and CONTmLLMAP
are used, if log-odds ratios, p-value densities or any other model specifies effect likelihoods. CONTmLLBayes
refers to an inference scheme, were the linking positions of effect reporters to network nodes are integrated out, and CONTmLLMAP
to an inference scheme, were a MAP estimate for the linking positions is calculated. depn
indicates Deterministic Effects Propagation Networks (DEPNs).
mLL
FULLmLL()
for binary data
depn
. Default: NULL
local.model.prior
according to arguments local.prior.size
and local.prior.bias
nemModelSelection
is used, Default: 0 (no regularization)
getRelevantEGenes
is called and a new model is trained on the selected E-genes. The process is then repeated until convergence. Default: "regularization"
nem.greedyMAP
and depn
. Default: TRUE
binary_ML
: effects come from a binomial distribution - ML learning of parameters (Bayesian networks only); binary_Bayesian
: effects come from a binomial distribution - Bayesian learning of parameters (Bayesian networks only); continuous_ML
: effects come from a normal distribution - ML learning of parameters; continuous_Bayesian
: effects come from a normal distribution - Bayesian learning of parameters.
depn
: For any perturbed node we suppose the unknown mean mu given its unknown variance sigma2 to be drawn from N(nu.intervention, sigma2/lambda.intervention). Default: nu.intervention=0.6, lambda.intervention=4
depn
: The unknown variance sigma2 for perturbed nodes is supposed to be drawn from Inv-$\chi^2$(df.intervention, scale.intervention). Default: df.intervention=4.4, scale.intervention=4.4
depn
: Mapping of interventions to network nodes. The format is a named list of strings with names being the interventions and entries being the network nodes. Default: Entries and names are the network nodes.
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Markowetz, F.; Kostka, D.; Troyanskaya, O. & Spang, R., Nested Effects Models for High-dimensional Phenotyping Screens. Bioinformatics, 2007, 23, i305 - i312\
Fr\"ohlich, H.; Fellmann, M.; S\"ultmann, H.; Poustka, A. & Beissbarth, T. Large Scale Statistical Inference of Signaling Pathways from RNAi and Microarray Data. BMC Bioinformatics, 2007, 8, 386\
Fr\"ohlich, H.; Fellmann, M.; S\"ultmann, H.; Poustka, A. & Beissbarth, T. Estimating Large Scale Signaling Networks through Nested Effect Models with Intervention Effects from Microarray Data. Bioinformatics, 2008, 24, 2650-2656\
Tresch, A. & Markowetz, F., Structure Learning in Nested Effects Models Statistical Applications in Genetics and Molecular Biology, 2008, 7\
Zeller, C.; Fr\"ohlich, H. & Tresch, A., A Bayesian Network View on Nested Effects Models EURASIP Journal on Bioinformatics and Systems Biology, 2009, 195272\
Fr\"ohlich, H.; Tresch, A. & Beissbarth, T., Nested Effects Models for Learning Signaling Networks from Perturbation Data. Biometrical Journal, 2009, 2, 304 - 323\
Fr\"ohlich, H.; Sahin, \"O.; Arlt, D.; Bender, C. & Beissbarth, T. Deterministic Effects Propagation Networks for Reconstructing Protein Signaling Networks from Multiple Interventions. BMC Bioinformatics, 2009, 10, 322\
Fr\"ohlich, H.; Praveen, P. & Tresch, A., Fast and Efficient Dynamic Nested Effects Models. Bioinformatics, 2011, 27, 238-244\
Niederberger, T.; Etzold, S.; Lidschreiber, M; Maier, K.; Martin, D.; Fr\"ohlich, H.; Cramer, P.; Tresch, A., MC Eminem Maps the Interaction Landscape of the Mediator, PLoS Comp. Biol., 2012, submitted.
control = set.default.parameters(LETTERS[1:5], type="CONTmLLBayes", selEGenes=TRUE) # set inference type and whether to use automatic E-gene selection for a network with nodes "A"-"E".
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