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rename pipeline function
1 parent bb9f977 commit f003b16

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NAMESPACE

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@@ -151,8 +151,8 @@ export(seurat_cluster)
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export(seurat_find_markers)
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export(seurat_integrate)
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export(seurat_integration_pipeline)
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export(seurat_pipeline)
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export(seurat_preprocess)
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export(seurat_process)
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export(seurat_reduce_dimensions)
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export(seurat_v5_integrate)
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export(seurat_v5_integration_pipeline)

R/docker_app.R

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@@ -338,7 +338,7 @@ dockerSeuratApp <- function(object = panc8, loom_path = NULL, appTitle = NULL,
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)
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seu(reintegrated_seu)
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} else {
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processed_seu <- seurat_pipeline(seu(), resolution = seq(0.2, 2, by = 0.2))
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processed_seu <- seurat_process(seu(), resolution = seq(0.2, 2, by = 0.2))
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seu(processed_seu)
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}
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message("Complete!")
@@ -372,7 +372,7 @@ dockerSeuratApp <- function(object = panc8, loom_path = NULL, appTitle = NULL,
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)
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seu(reintegrated_seu)
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} else {
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processed_seu <- seurat_pipeline(seu(), resolution = seq(0.2, 2, by = 0.2))
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processed_seu <- seurat_process(seu(), resolution = seq(0.2, 2, by = 0.2))
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seu(processed_seu)
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}
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message("Complete!")

R/minimal_app.R

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@@ -339,7 +339,7 @@ minimalSeuratApp <- function(object = panc8, loom_path = NULL, appTitle = NULL,
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)
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seu(reintegrated_seu)
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} else {
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processed_seu <- seurat_pipeline(seu(), resolution = seq(0.2, 2, by = 0.2))
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processed_seu <- seurat_process(seu(), resolution = seq(0.2, 2, by = 0.2))
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seu(processed_seu)
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}
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message("Complete!")
@@ -373,7 +373,7 @@ minimalSeuratApp <- function(object = panc8, loom_path = NULL, appTitle = NULL,
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)
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seu(reintegrated_seu)
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} else {
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processed_seu <- seurat_pipeline(seu(), resolution = seq(0.2, 2, by = 0.2))
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processed_seu <- seurat_process(seu(), resolution = seq(0.2, 2, by = 0.2))
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seu(processed_seu)
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}
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message("Complete!")

R/pipeline.R

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@@ -142,16 +142,16 @@ seurat_v5_integration_pipeline <- function(seu, resolution = seq(0.2, 2.0, by =
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#' @param resolution Resolution for clustering cells. Default set to 0.6.
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#' @param reduction Dimensional reduction object seu
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#' @param organism Organism
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#' @param ... Extra parameters passed to seurat_pipeline
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#' @param ... Extra parameters passed to seurat_process
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#'
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#' @return
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#' @export
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#'
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#' @examples
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#'
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#' processed_seu <- seurat_pipeline(panc8)
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#' processed_seu <- seurat_process(panc8)
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#'
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seurat_pipeline <- function(seu, assay = "gene", resolution = 0.6, reduction = "pca", organism = "human", ...) {
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seurat_process <- function(seu, assay = "gene", resolution = 0.6, reduction = "pca", organism = "human", ...) {
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assays <- names(seu@assays)
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assays <- assays[assays %in% c("gene", "transcript")]

R/seurat_app.R

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Original file line numberDiff line numberDiff line change
@@ -714,7 +714,7 @@ seuratApp <- function(preset_project, appTitle = "seuratTools", organism_type =
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)
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seu(reintegrated_seu)
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} else {
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subset_seu <- seurat_pipeline(seu(), resolution = seq(0.2, 2, by = 0.2), legacy_settings = input$legacySettingsSubset) # markermarker
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subset_seu <- seurat_process(seu(), resolution = seq(0.2, 2, by = 0.2), legacy_settings = input$legacySettingsSubset) # markermarker
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seu(subset_seu)
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}
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message("Complete!")
@@ -748,7 +748,7 @@ seuratApp <- function(preset_project, appTitle = "seuratTools", organism_type =
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)
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seu(reintegrated_seu)
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} else {
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subset_seu <- seurat_pipeline(seu(),
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subset_seu <- seurat_process(seu(),
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resolution = seq(0.2,
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2,
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by = 0.2

R/workflow.R

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@@ -78,7 +78,7 @@ integration_workflow <- function(batches, excluded_cells = NULL, resolution = se
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#' clustered_human_seu <- clustering_workflow(panc8, experiment_name = "seurat_pancreas", organism = "human")
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#' clustered_mouse_seu <- clustering_workflow(baron2016singlecell)
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clustering_workflow <- function(seu, excluded_cells, resolution = seq(0.2, 2.0, by = 0.2), organism = "human", experiment_name = "default_experiment", ...) {
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seu <- seurat_pipeline(seu, resolution = resolution, organism = organism, ...)
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seu <- seurat_process(seu, resolution = resolution, organism = organism, ...)
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seu <- record_experiment_data(seu, experiment_name, organism)
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man/add_census_slot.Rd

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man/convert_monoclev2_to_seuv3.Rd

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man/convert_seuv3_to_monoclev2.Rd

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man/plot_all_ptimes.Rd

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