twosigma: Fit the TWO-SIGMA Model.

In edvanburen/twosigma: DE Analysis for Single-Cell RNA-Sequencing Data

Fit the TWO-SIGMA Model.

Description

Fit the TWO-SIGMA Model.

Usage

twosigma(
  count_matrix,
  mean_covar,
  zi_covar,
  mean_re = TRUE,
  zi_re = TRUE,
  id,
  adhoc = TRUE,
  adhoc_thresh = 0.1,
  return_summary_fits = TRUE,
  disp_covar = NULL,
  weights = rep(1, ncol(count_matrix)),
  control = glmmTMBControl(),
  ncores = 1,
  cluster_type = "Fork",
  chunk_size = 10,
  lb = FALSE
)

Arguments

count_matrix	Matrix of non-negative integer read counts, with rows corresponding to genes and columns corresponding to cells. It is recommended to make the rownames the gene names for better output.
mean_covar	Covariates for the (conditional) mean model. Must be a matrix (without an intercept column) or = 1 to indicate an intercept only model.
zi_covar	Covariates for the zero-inflation model. Must be a matrix (without an intercept column), = 1 to indicate an intercept only model, or = 0 to indicate no zero-inflation model desired.
mean_re	Should random intercepts be included in the (conditional) mean model? Ignored if adhoc=TRUE.
zi_re	Should random intercepts be included in the zero-inflation model? Ignored if adhoc=TRUE.
id	Vector of individual-level ID's. Used for random effect prediction and the adhoc method but required regardless.
adhoc	Should the adhoc method be used by default to judge if random effects are needed?
adhoc_thresh	Value below which the adhoc p-value is deemed significant (and thus RE are deemed necessary). Only used if adhoc==TRUE.
return_summary_fits	If TRUE, the package returns a summary.glmmTMB object for each gene. If FALSE, an object of class glmmTMB is returned for each gene. The latter requires far more memory to store.
disp_covar	Covariates for a log-linear model for the dispersion. Either a matrix of covariates or = 1 to indicate an intercept only model. Random effect terms are not permitted in the dispersion model. Defaults to NULL for constant dispersion.
weights	weights, as in glm. Defaults to 1 for all observations and no scaling or centering of weights is performed.
control	Control parameters for optimization in glmmTMB. See ?glmmTMBControl.
ncores	Number of cores used for parallelization. Defaults to 1, meaning no parallelization of any kind is done.
cluster_type	Whether to use a "cluster of type "Fork" or "Sock". On Unix systems, "Fork" will likely improve performance. On Windows, only "Sock" will actually result in parallelized computing.
chunk_size	Number of genes to be sent to each parallel environment. Parallelization is more efficient, particularly with a large count matrix, when the count matrix is 'chunked' into some common size (e.g. 10, 50, 200). Defaults to 10.
lb	Should load balancing be used for parallelization? Users will likely want to set to FALSE for improved performance.

Value

A list with the following elements: ##'

• fit: If return_summary_fits=TRUE, returns a list of model fit objects of class summary.glmmTMB. If return_summary_fits=FALSE, returns a list of model fit objects of class glmmTMB. In either case, the order matches the row order of count_matrix, and the names of the list elements are taken as the rownames of count_matrix.

• adhoc_include_RE: Logical vector indicator whether the adhoc method determined random effects needed. If adhoc=F, then a vector of NA's.

• gene_error: Vector indicating whether the particular gene produced an error during model fitting (TRUE) or not (FALSE).

Details

If adhoc=TRUE, any input in mean_re and zi_re will be ignored.

Examples

# Set Parameters to Simulate Some Data

nind<-10;ncellsper<-rep(50,nind)
sigma.a<-.5;sigma.b<-.5;phi<-.1
alpha<-c(1,0,-.5,-2);beta<-c(2,0,-.1,.6)
beta2<-c(2,1,-.1,.6)
id.levels<-1:nind;nind<-length(id.levels)
id<-rep(id.levels,times=ncellsper)
sim.seed<-1234

# Simulate individual level covariates

t2d_sim<-rep(rbinom(nind,1,p=.4),times=ncellsper)
cdr_sim<-rbeta(sum(ncellsper),3,6)
age_sim<-rep(sample(c(20:60),size=nind,replace = TRUE),times=ncellsper)

# Construct design matrices

Z<-cbind(scale(t2d_sim),scale(age_sim),scale(cdr_sim))
colnames(Z)<-c("t2d_sim","age_sim","cdr_sim")
X<-cbind(scale(t2d_sim),scale(age_sim),scale(cdr_sim))
colnames(X)<-c("t2d_sim","age_sim","cdr_sim")

# Simulate Data

sim_dat<-matrix(nrow=2,ncol=sum(ncellsper))
for(i in 1:nrow(sim_dat)){
   sim_dat[i,]<-simulate_zero_inflated_nb_random_effect_data(ncellsper,X,Z,alpha,beta2
   ,phi,sigma.a,sigma.b,id.levels=NULL)$Y
}
rownames(sim_dat)<-paste("Gene",1:2)

# Run twosigma

twosigma(sim_dat[1:2,],mean_covar = X,zi_covar=1,id = id)

edvanburen/twosigma documentation built on July 3, 2023, 3:39 p.m.