R/RcppExports.R

In mayer-lab/SeuratForMayer2018: Seurat : R Toolkit for Single Cell Genomics

# Generated by using Rcpp::compileAttributes() -> do not edit by hand
# Generator token: 10BE3573-1514-4C36-9D1C-5A225CD40393

RunUMISampling <- function(data, sample_val, upsample = FALSE, display_progress = TRUE) {
    .Call('_Seurat_RunUMISampling', PACKAGE = 'Seurat', data, sample_val, upsample, display_progress)
}

RunUMISamplingPerCell <- function(data, sample_val, upsample = FALSE, display_progress = TRUE) {
    .Call('_Seurat_RunUMISamplingPerCell', PACKAGE = 'Seurat', data, sample_val, upsample, display_progress)
}

RowMergeMatrices <- function(mat1, mat2, mat1_rownames, mat2_rownames, all_rownames) {
    .Call('_Seurat_RowMergeMatrices', PACKAGE = 'Seurat', mat1, mat2, mat1_rownames, mat2_rownames, all_rownames)
}

LogNorm <- function(data, scale_factor, display_progress = TRUE) {
    .Call('_Seurat_LogNorm', PACKAGE = 'Seurat', data, scale_factor, display_progress)
}

FastMatMult <- function(m1, m2) {
    .Call('_Seurat_FastMatMult', PACKAGE = 'Seurat', m1, m2)
}

FastRowScale <- function(mat, scale = TRUE, center = TRUE, scale_max = 10, display_progress = TRUE) {
    .Call('_Seurat_FastRowScale', PACKAGE = 'Seurat', mat, scale, center, scale_max, display_progress)
}

Standardize <- function(mat, display_progress = TRUE) {
    .Call('_Seurat_Standardize', PACKAGE = 'Seurat', mat, display_progress)
}

FastSparseRowScale <- function(mat, scale = TRUE, center = TRUE, scale_max = 10, display_progress = TRUE) {
    .Call('_Seurat_FastSparseRowScale', PACKAGE = 'Seurat', mat, scale, center, scale_max, display_progress)
}

FastCov <- function(mat, center = TRUE) {
    .Call('_Seurat_FastCov', PACKAGE = 'Seurat', mat, center)
}

FastCovMats <- function(mat1, mat2, center = TRUE) {
    .Call('_Seurat_FastCovMats', PACKAGE = 'Seurat', mat1, mat2, center)
}

FastRBind <- function(mat1, mat2) {
    .Call('_Seurat_FastRBind', PACKAGE = 'Seurat', mat1, mat2)
}