| mcmc.sampler | R Documentation | 
Function for fitting sBFAC model via MCMC methods.
mcmc.sampler(facfit, Y, X, w0, g0, mcmc, thinstep)
| facfit | MAP estimates of sBFAC used to initialize MCMC algorithm. | 
| Y | Expression data in samples by features format | 
| X | Design matrix from model.matrix function which defines how covariates are included into sBFAC. | 
| w0 | Controls sparseness in features, minimum value should be 0.01 for non-informative priors. | 
| g0 | Decreasing this regularize regression coefficients, i.e., g0=1000 provides non-informative prior == Classical estimates | 
| mcmc | Number of MCMC samples. Default is 20000 but can be increased to improve convergence. | 
| thinstep | Number of iterations to thin to remove autocorrelation between samples. | 
Function for fitting sBFAC model via MCMC methods.
| scores.store  | This is an array of qxNxmcmc containing scores for the q latent variables on N obaservations over mcmc samples. | 
| loadings.store  | This is an array of pxqxmcmc containing loadings for the p genes/features on q latent variables over mcmc samples. | 
| beta.store  | This is an array of qxLxmcmc containing regression coefficients of L covariates on q latent variables over mcmc samples. | 
| sigma.store  | This is an matrix of pxmcmc containing residual variablity of each feature. | 
| s2.store  | This is an matrix of qxmcmc containing residual variablity of each latent variable. | 
Gift Nyamundanda, Katie Eason, Pawan Poudel and Anguraj Sadanandam.
Nyamundanda et al (2015). A next generation tool enables identification of functional cancer subtypes with associated biological phenotypes.
## help(mcmc.sampler)
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