interaction between CytoPipeline object and disk cache — interactingWithCytoPipelineCache • CytoPipeline

functions supporting the interaction between a CytoPipeline object and the file cache on disk

Usage

deleteCytoPipelineCache(x, path = ".")

buildCytoPipelineFromCache(experimentName, path = ".")

checkCytoPipelineConsistencyWithCache(
  x,
  path = ".",
  whichQueue = c("both", "scale transform", "pre-processing"),
  sampleFile = NULL
)

Arguments

x: a CytoPipeline object
path: the full path to the experiment storage on disk (without the /.cache)
experimentName: the experimentName used to select the file cache on disk
whichQueue: which processing queue to check the consistency of
sampleFile: if whichQueue == "pre-processing" or "both": which sample file(s) to check on the disk cache

Value

for deleteCytoPipelineCache: TRUE if successfully removed
for buildCytoPipelineFromCache: the built CytoPipeline object
for checkCytoPipelineConsistencyWithCache: a list with the following values:

isConsistent (TRUE/FALSE)
inconsistencyMsg: character filled in by an inconsistency message in case the cache and CytoPipeline object are not consistent with each other
scaleTransformStepStatus: a character vector, containing, for each scale transform step, a status from c("run", "not run", "inconsistent")
preProcessingStepStatus: a character matrix, containing, for each pre-processing step (rows), for each sample file (columns), a status from c("run", "not run", "inconsistent")

Functions

deleteCytoPipelineCache(): delete the whole disk cache corresponding to the experiment of a CytoPipeline object
buildCytoPipelineFromCache(): builds a new CytoPipeline object, based on the information stored in the file cache
checkCytoPipelineConsistencyWithCache(): check the consistency between the processing steps described in a CytoPipeline object, and what is stored in the file cache

Examples


# preliminary run:
# build CytoPipeline object using json input, run and store results in cache
rawDataDir <-
    system.file("extdata", package = "CytoPipeline")
experimentName <- "OMIP021_PeacoQC"
sampleFiles <- file.path(rawDataDir, list.files(rawDataDir,
                                             pattern = "Donor"))
                                             
jsonDir <- system.file("extdata", package = "CytoPipeline")
jsonPath <- file.path(jsonDir, "pipelineParams.json")
outputDir <- base::tempdir()
pipL <- CytoPipeline(jsonPath,
                     experimentName = experimentName,
                     sampleFiles = sampleFiles)

# note we temporarily set working directory into package root directory
# needed as json path mentions "./" path for sample files
suppressWarnings(execute(pipL, rmCache = TRUE, path = outputDir))
#> #####################################################
#> ### running SCALE TRANSFORMATION processing steps ###
#> #####################################################
#> Proceeding with step 1 [flowframe_read] ...
#> Proceeding with step 2 [remove_margins] ...
#> Removing margins from file : Donor1.fcs
#> Removing margins from file : Donor2.fcs
#> Proceeding with step 3 [compensate] ...
#> Proceeding with step 4 [flowframe_aggregate] ...
#> Proceeding with step 5 [scale_transform_estimate] ...
#> #####################################################
#> ### NOW PRE-PROCESSING FILE /__w/_temp/Library/CytoPipeline/extdata/Donor1.fcs...
#> #####################################################
#> Proceeding with step 1 [flowframe_read] ...
#> Proceeding with step 2 [remove_margins] ...
#> Removing margins from file : Donor1.fcs
#> Proceeding with step 3 [compensate] ...
#> Proceeding with step 4 [remove_doublets] ...
#> Proceeding with step 5 [remove_debris] ...
#> Proceeding with step 6 [remove_dead_cells] ...
#> Proceeding with step 7 [perform_QC] ...
#> Applying PeacoQC method...
#> Starting quality control analysis for Donor1.fcs
#> Calculating peaks
#> MAD analysis removed 30.75% of the measurements
#> The algorithm removed 30.75% of the measurements
#> Proceeding with step 8 [transform] ...
#> #####################################################
#> ### NOW PRE-PROCESSING FILE /__w/_temp/Library/CytoPipeline/extdata/Donor2.fcs...
#> #####################################################
#> Proceeding with step 1 [flowframe_read] ...
#> Proceeding with step 2 [remove_margins] ...
#> Removing margins from file : Donor2.fcs
#> Proceeding with step 3 [compensate] ...
#> Proceeding with step 4 [remove_doublets] ...
#> Proceeding with step 5 [remove_debris] ...
#> Proceeding with step 6 [remove_dead_cells] ...
#> Proceeding with step 7 [perform_QC] ...
#> Applying PeacoQC method...
#> Starting quality control analysis for Donor2.fcs
#> Calculating peaks
#> MAD analysis removed 24.38% of the measurements
#> The algorithm removed 24.38% of the measurements
#> Proceeding with step 8 [transform] ...
     

# rebuild CytoPipeline from stored results in cache, for a specific 
# experiment

experimentName <- "OMIP021_PeacoQC"
pipL2 <- buildCytoPipelineFromCache(
    experimentName = experimentName,
    path = outputDir)


# checking consistency between CytoPipeline object and cache
res <- checkCytoPipelineConsistencyWithCache(pipL2)
#res

suppressWarnings(execute(pipL2, rmCache = FALSE, path = outputDir))
#> #####################################################
#> ### running SCALE TRANSFORMATION processing steps ###
#> #####################################################
#> Proceeding with step 1 [flowframe_read]: found in cache!
#> Proceeding with step 2 [remove_margins]: found in cache!
#> Proceeding with step 3 [compensate]: found in cache!
#> Proceeding with step 4 [flowframe_aggregate]: found in cache!
#> Proceeding with step 5 [scale_transform_estimate]: found in cache!
#> #####################################################
#> ### NOW PRE-PROCESSING FILE Donor1.fcs...
#> #####################################################
#> Proceeding with step 1 [flowframe_read]: found in cache!
#> Proceeding with step 2 [remove_margins]: found in cache!
#> Proceeding with step 3 [compensate]: found in cache!
#> Proceeding with step 4 [remove_doublets]: found in cache!
#> Proceeding with step 5 [remove_debris]: found in cache!
#> Proceeding with step 6 [remove_dead_cells]: found in cache!
#> Proceeding with step 7 [perform_QC]: found in cache!
#> Proceeding with step 8 [transform]: found in cache!
#> #####################################################
#> ### NOW PRE-PROCESSING FILE Donor2.fcs...
#> #####################################################
#> Proceeding with step 1 [flowframe_read]: found in cache!
#> Proceeding with step 2 [remove_margins]: found in cache!
#> Proceeding with step 3 [compensate]: found in cache!
#> Proceeding with step 4 [remove_doublets]: found in cache!
#> Proceeding with step 5 [remove_debris]: found in cache!
#> Proceeding with step 6 [remove_dead_cells]: found in cache!
#> Proceeding with step 7 [perform_QC]: found in cache!
#> Proceeding with step 8 [transform]: found in cache!
# (everything is already stored in cache)

# deleting cache related to a specific experiment
pipL3 <- CytoPipeline(experimentName = experimentName)
deleteCytoPipelineCache(pipL3, path = outputDir)
#> [1] TRUE