### config file for TIAN dataset
proj.name <- "cell_lines"
data.folder <- file.path("examples", "data", proj.name)
fig.folder <- file.path("examples", "plots", proj.name)
.seed.seq <- c(12345, 111, 19, 42, 7, 559241, 123, 987, 234, 91, 877, 451, 817)
.seed <- .seed.seq[1]
.N.clusters.seq <- 2:10
.N.clusters.seq.breaks <- unique(c(0, seq(2, max(.N.clusters.seq), 2), max(.N.clusters.seq)))
.gamma.seq <- c(1, 2, 5, 10, 20, 50, 100, 200)
.N.var.genes <- 1000
.genes.use <- NULL
.genes.omit <- NULL
.N.comp <- 10
.approx.N <- 1000
.k.knn <- 5
.SELECTED_METHODS <- c("Exact", "Random", "Subsampling", "Metacell")
.logFC.thresh <- 0.5
.pval.thresh <- 0.05
.logFC.thresh.SC <- 0.25
.do.extra.log.rescale <- FALSE
.do.extra.sqrt.rescale <- FALSE
.do.frames <- TRUE
.min.SC.size.to.plot <- c(0, 0, 0, 0, 0, 0, 0, 0)+1
names(.min.SC.size.to.plot) <- as.character(.gamma.seq)
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