Back to Multiple platform build/check report for BioC 3.17:   simplified   long
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This page was generated on 2023-10-16 11:36:58 -0400 (Mon, 16 Oct 2023).

HostnameOSArch (*)R versionInstalled pkgs
nebbiolo1Linux (Ubuntu 22.04.2 LTS)x86_644.3.1 (2023-06-16) -- "Beagle Scouts" 4626
palomino3Windows Server 2022 Datacenterx644.3.1 (2023-06-16 ucrt) -- "Beagle Scouts" 4379
merida1macOS 12.6.4 Montereyx86_644.3.1 (2023-06-16) -- "Beagle Scouts" 4395
Click on any hostname to see more info about the system (e.g. compilers)      (*) as reported by 'uname -p', except on Windows and Mac OS X

Package 487/2230HostnameOS / ArchINSTALLBUILDCHECKBUILD BIN
CytoPipeline 1.0.2  (landing page)
Philippe Hauchamps
Snapshot Date: 2023-10-15 14:00:13 -0400 (Sun, 15 Oct 2023)
git_url: https://git.bioconductor.org/packages/CytoPipeline
git_branch: RELEASE_3_17
git_last_commit: 1e0e5f8
git_last_commit_date: 2023-07-04 08:00:48 -0400 (Tue, 04 Jul 2023)
nebbiolo1Linux (Ubuntu 22.04.2 LTS) / x86_64  OK    OK    OK  UNNEEDED, same version is already published
palomino3Windows Server 2022 Datacenter / x64  OK    OK    OK    OK  UNNEEDED, same version is already published
merida1macOS 12.6.4 Monterey / x86_64  OK    OK    OK    OK  UNNEEDED, same version is already published
kjohnson2macOS 12.6.1 Monterey / arm64see weekly results here

CHECK results for CytoPipeline on merida1


To the developers/maintainers of the CytoPipeline package:
- Allow up to 24 hours (and sometimes 48 hours) for your latest push to git@git.bioconductor.org:packages/CytoPipeline.git to reflect on this report. See Troubleshooting Build Report for more information.
- Use the following Renviron settings to reproduce errors and warnings.
- If 'R CMD check' started to fail recently on the Linux builder(s) over a missing dependency, add the missing dependency to 'Suggests:' in your DESCRIPTION file. See Renviron.bioc for more information.

raw results


Summary

Package: CytoPipeline
Version: 1.0.2
Command: /Library/Frameworks/R.framework/Resources/bin/R CMD check --install=check:CytoPipeline.install-out.txt --library=/Library/Frameworks/R.framework/Resources/library --no-vignettes --timings CytoPipeline_1.0.2.tar.gz
StartedAt: 2023-10-16 00:34:54 -0400 (Mon, 16 Oct 2023)
EndedAt: 2023-10-16 00:45:27 -0400 (Mon, 16 Oct 2023)
EllapsedTime: 632.5 seconds
RetCode: 0
Status:   OK  
CheckDir: CytoPipeline.Rcheck
Warnings: 0

Command output

##############################################################################
##############################################################################
###
### Running command:
###
###   /Library/Frameworks/R.framework/Resources/bin/R CMD check --install=check:CytoPipeline.install-out.txt --library=/Library/Frameworks/R.framework/Resources/library --no-vignettes --timings CytoPipeline_1.0.2.tar.gz
###
##############################################################################
##############################################################################


* using log directory ‘/Users/biocbuild/bbs-3.17-bioc/meat/CytoPipeline.Rcheck’
* using R version 4.3.1 (2023-06-16)
* using platform: x86_64-apple-darwin20 (64-bit)
* R was compiled by
    Apple clang version 14.0.3 (clang-1403.0.22.14.1)
    GNU Fortran (GCC) 12.2.0
* running under: macOS Monterey 12.6.4
* using session charset: UTF-8
* using option ‘--no-vignettes’
* checking for file ‘CytoPipeline/DESCRIPTION’ ... OK
* this is package ‘CytoPipeline’ version ‘1.0.2’
* package encoding: UTF-8
* checking package namespace information ... OK
* checking package dependencies ... OK
* checking if this is a source package ... OK
* checking if there is a namespace ... OK
* checking for hidden files and directories ... OK
* checking for portable file names ... OK
* checking for sufficient/correct file permissions ... OK
* checking whether package ‘CytoPipeline’ can be installed ... OK
* checking installed package size ... OK
* checking package directory ... OK
* checking ‘build’ directory ... OK
* checking DESCRIPTION meta-information ... OK
* checking top-level files ... NOTE
File
  LICENSE
is not mentioned in the DESCRIPTION file.
* checking for left-over files ... OK
* checking index information ... OK
* checking package subdirectories ... OK
* checking R files for non-ASCII characters ... OK
* checking R files for syntax errors ... OK
* checking whether the package can be loaded ... OK
* checking whether the package can be loaded with stated dependencies ... OK
* checking whether the package can be unloaded cleanly ... OK
* checking whether the namespace can be loaded with stated dependencies ... OK
* checking whether the namespace can be unloaded cleanly ... OK
* checking dependencies in R code ... OK
* checking S3 generic/method consistency ... OK
* checking replacement functions ... OK
* checking foreign function calls ... OK
* checking R code for possible problems ... OK
* checking Rd files ... OK
* checking Rd metadata ... OK
* checking Rd cross-references ... OK
* checking for missing documentation entries ... OK
* checking for code/documentation mismatches ... OK
* checking Rd \usage sections ... OK
* checking Rd contents ... OK
* checking for unstated dependencies in examples ... OK
* checking contents of ‘data’ directory ... OK
* checking data for non-ASCII characters ... OK
* checking data for ASCII and uncompressed saves ... OK
* checking files in ‘vignettes’ ... OK
* checking examples ... OK
Examples with CPU (user + system) or elapsed time > 5s
                                   user system elapsed
execute                          47.570  2.670  71.406
interactingWithCytoPipelineCache 25.267  1.305  35.922
inspectCytoPipelineObjects       17.251  0.882  24.782
ggplotEvents                      9.138  0.164  12.896
qualityControlFlowAI              6.496  0.410   8.836
* checking for unstated dependencies in ‘tests’ ... OK
* checking tests ...
  Running ‘testthat.R’
 OK
* checking for unstated dependencies in vignettes ... OK
* checking package vignettes in ‘inst/doc’ ... OK
* checking running R code from vignettes ... SKIPPED
* checking re-building of vignette outputs ... SKIPPED
* checking PDF version of manual ... OK
* DONE

Status: 1 NOTE
See
  ‘/Users/biocbuild/bbs-3.17-bioc/meat/CytoPipeline.Rcheck/00check.log’
for details.



Installation output

CytoPipeline.Rcheck/00install.out

##############################################################################
##############################################################################
###
### Running command:
###
###   /Library/Frameworks/R.framework/Resources/bin/R CMD INSTALL CytoPipeline
###
##############################################################################
##############################################################################


* installing to library ‘/Library/Frameworks/R.framework/Versions/4.3-x86_64/Resources/library’
* installing *source* package ‘CytoPipeline’ ...
** using staged installation
** R
** data
** inst
** byte-compile and prepare package for lazy loading
** help
*** installing help indices
** building package indices
** installing vignettes
** testing if installed package can be loaded from temporary location
** testing if installed package can be loaded from final location
** testing if installed package keeps a record of temporary installation path
* DONE (CytoPipeline)

Tests output

CytoPipeline.Rcheck/tests/testthat.Rout


R version 4.3.1 (2023-06-16) -- "Beagle Scouts"
Copyright (C) 2023 The R Foundation for Statistical Computing
Platform: x86_64-apple-darwin20 (64-bit)

R is free software and comes with ABSOLUTELY NO WARRANTY.
You are welcome to redistribute it under certain conditions.
Type 'license()' or 'licence()' for distribution details.

R is a collaborative project with many contributors.
Type 'contributors()' for more information and
'citation()' on how to cite R or R packages in publications.

Type 'demo()' for some demos, 'help()' for on-line help, or
'help.start()' for an HTML browser interface to help.
Type 'q()' to quit R.

> # CytoPipeline - Copyright (C) <2022>
> # <Université catholique de Louvain (UCLouvain), Belgique>
> #
> #   Description and complete License: see LICENSE file.
> #
> # This program (CytoPipeline) is free software:
> #   you can redistribute it and/or modify it under the terms of the GNU General
> # Public License as published by the Free Software Foundation,
> # either version 3 of the License, or (at your option) any later version.
> #
> # This program is distributed in the hope that it will be useful,
> # but WITHOUT ANY WARRANTY; without even the implied warranty of
> # MERCHANTABILITY or FITNESS FOR A PARTICULAR PURPOSE.  See the
> # GNU General Public License for more details (<http://www.gnu.org/licenses/>).
> 
> library(testthat)
> library(CytoPipeline)
> 
> # launch unit tests
> test_check("CytoPipeline")
Pipeline object for flow cytometry experiment: OMIP021_PeacoQC 
No sample file
No pheno data
Scale transformations evaluation queue has no processing step
Flow frames pre-processing evaluation queue has no processing step
Pipeline object for flow cytometry experiment: OMIP021_PeacoQC 
Sample files: 2 sample file(s)
No pheno data
Scale transformations evaluation queue has no processing step
Flow frames pre-processing evaluation queue has no processing step
#####################################################
### running SCALE TRANSFORMATION processing steps ###
#####################################################
Proceeding with step 1 [scale_transform_read] ...
#####################################################
### NOW PRE-PROCESSING FILE /Library/Frameworks/R.framework/Versions/4.3-x86_64/Resources/library/CytoPipeline/extdata/Donor1.fcs...
#####################################################
#####################################################
### NOW PRE-PROCESSING FILE /Library/Frameworks/R.framework/Versions/4.3-x86_64/Resources/library/CytoPipeline/extdata/Donor2.fcs...
#####################################################
Proceeding with phenoData ...
#####################################################
### running SCALE TRANSFORMATION processing steps ###
#####################################################
Proceeding with step 1 [flowframe_read] ...
#####################################################
### NOW PRE-PROCESSING FILE /Library/Frameworks/R.framework/Versions/4.3-x86_64/Resources/library/CytoPipeline/extdata/Donor1.fcs...
#####################################################
#####################################################
### NOW PRE-PROCESSING FILE /Library/Frameworks/R.framework/Versions/4.3-x86_64/Resources/library/CytoPipeline/extdata/Donor2.fcs...
#####################################################
#####################################################
### 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] ...
Compensating file : Donor1.fcs
Compensating file : Donor2.fcs
Proceeding with step 4 [flowframe_aggregate] ...
Proceeding with step 5 [scale_transform_estimate] ...
estimating logicle transformations for fluorochrome channels...
Estimating linear transformation for scatter channels : reference marker = BV785 - CD3...
applying specific linear transformation for FSC-A channel...
initial quantiles : q5 = 48809.1266 ; q95 = 182769.1664
target quantiles : q5 = 0.3996 ; q95 = 2.9603
a = 1.91e-05 ; b = -5.33e-01
applying FSC-A linear transformation for FSC-H channel...
applying specific linear transformation for SSC-A channel...
initial quantiles : q5 = 41296.8164 ; q95 = 223620.1273
target quantiles : q5 = 0.3996 ; q95 = 2.9603
a = 1.40e-05 ; b = -1.80e-01
applying SSC-A linear transformation for SSC-H channel...
#####################################################
### NOW PRE-PROCESSING FILE /Library/Frameworks/R.framework/Versions/4.3-x86_64/Resources/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] ...
Compensating file : Donor1.fcs
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

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MAD analysis removed 22.09% of the measurements
The algorithm removed 22.09% of the measurements
Proceeding with step 8 [transform] ...
#####################################################
### NOW PRE-PROCESSING FILE /Library/Frameworks/R.framework/Versions/4.3-x86_64/Resources/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] ...
Compensating file : Donor2.fcs
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

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MAD analysis removed 1.69% of the measurements
The algorithm removed 1.69% of the measurements
Proceeding with step 8 [transform] ...
#####################################################
### 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 /Library/Frameworks/R.framework/Versions/4.3-x86_64/Resources/library/CytoPipeline/extdata/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 /Library/Frameworks/R.framework/Versions/4.3-x86_64/Resources/library/CytoPipeline/extdata/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!
#####################################################
### 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] ...
Compensating file : Donor1.fcs
Compensating file : Donor2.fcs
Proceeding with step 4 [flowframe_aggregate] ...
Proceeding with step 5 [scale_transform_estimate] ...
estimating logicle transformations for fluorochrome channels...
Estimating linear transformation for scatter channels : reference marker = BV785 - CD3...
applying specific linear transformation for FSC-A channel...
initial quantiles : q5 = 48809.1266 ; q95 = 182769.1664
target quantiles : q5 = 0.3996 ; q95 = 2.9603
a = 1.91e-05 ; b = -5.33e-01
applying FSC-A linear transformation for FSC-H channel...
applying specific linear transformation for SSC-A channel...
initial quantiles : q5 = 41296.8164 ; q95 = 223620.1273
target quantiles : q5 = 0.3996 ; q95 = 2.9603
a = 1.40e-05 ; b = -1.80e-01
applying SSC-A linear transformation for SSC-H channel...
#####################################################
### NOW PRE-PROCESSING FILE /Library/Frameworks/R.framework/Versions/4.3-x86_64/Resources/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] ...
Compensating file : Donor1.fcs
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

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MAD analysis removed 22.09% of the measurements
The algorithm removed 22.09% of the measurements
Proceeding with step 8 [transform] ...
#####################################################
### NOW PRE-PROCESSING FILE /Library/Frameworks/R.framework/Versions/4.3-x86_64/Resources/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] ...
Compensating file : Donor2.fcs
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

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MAD analysis removed 1.69% of the measurements
The algorithm removed 1.69% of the measurements
Proceeding with step 8 [transform] ...
#####################################################
### 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] ...
Compensating file : Donor1.fcs
Compensating file : Donor2.fcs
Proceeding with step 4 [flowframe_aggregate] ...
Proceeding with step 5 [scale_transform_estimate] ...
estimating logicle transformations for fluorochrome channels...
Estimating linear transformation for scatter channels : reference marker = BV785 - CD3...
applying specific linear transformation for FSC-A channel...
initial quantiles : q5 = 48809.1266 ; q95 = 182769.1664
target quantiles : q5 = 0.3996 ; q95 = 2.9603
a = 1.91e-05 ; b = -5.33e-01
applying FSC-A linear transformation for FSC-H channel...
applying specific linear transformation for SSC-A channel...
initial quantiles : q5 = 41296.8164 ; q95 = 223620.1273
target quantiles : q5 = 0.3996 ; q95 = 2.9603
a = 1.40e-05 ; b = -1.80e-01
applying SSC-A linear transformation for SSC-H channel...
#####################################################
### NOW PRE-PROCESSING FILE /Library/Frameworks/R.framework/Versions/4.3-x86_64/Resources/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] ...
Compensating file : Donor1.fcs
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

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  |+++++++++++++++++++++++++++++++++++++++++++++     |  90%
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  |++++++++++++++++++++++++++++++++++++++++++++++++  |  95%
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  |++++++++++++++++++++++++++++++++++++++++++++++++++| 100%
MAD analysis removed 22.09% of the measurements
The algorithm removed 22.09% of the measurements
Proceeding with step 8 [transform] ...
#####################################################
### NOW PRE-PROCESSING FILE /Library/Frameworks/R.framework/Versions/4.3-x86_64/Resources/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] ...
Compensating file : Donor2.fcs
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

  |                                                        
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  |++                                                |   5%
  |                                                        
  |+++++                                             |  10%
  |                                                        
  |++++++++                                          |  15%
  |                                                        
  |++++++++++                                        |  20%
  |                                                        
  |++++++++++++                                      |  25%
  |                                                        
  |+++++++++++++++                                   |  30%
  |                                                        
  |++++++++++++++++++                                |  35%
  |                                                        
  |++++++++++++++++++++                              |  40%
  |                                                        
  |++++++++++++++++++++++                            |  45%
  |                                                        
  |+++++++++++++++++++++++++                         |  50%
  |                                                        
  |++++++++++++++++++++++++++++                      |  55%
  |                                                        
  |++++++++++++++++++++++++++++++                    |  60%
  |                                                        
  |++++++++++++++++++++++++++++++++                  |  65%
  |                                                        
  |+++++++++++++++++++++++++++++++++++               |  70%
  |                                                        
  |++++++++++++++++++++++++++++++++++++++            |  75%
  |                                                        
  |++++++++++++++++++++++++++++++++++++++++          |  80%
  |                                                        
  |++++++++++++++++++++++++++++++++++++++++++        |  85%
  |                                                        
  |+++++++++++++++++++++++++++++++++++++++++++++     |  90%
  |                                                        
  |++++++++++++++++++++++++++++++++++++++++++++++++  |  95%
  |                                                        
  |++++++++++++++++++++++++++++++++++++++++++++++++++| 100%
MAD analysis removed 1.69% of the measurements
The algorithm removed 1.69% of the measurements
Proceeding with step 8 [transform] ...
#####################################################
### 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] ...
Compensating file : Donor1.fcs
Compensating file : Donor2.fcs
Proceeding with step 4 [flowframe_aggregate] ...
Proceeding with step 5 [scale_transform_estimate] ...
estimating logicle transformations for fluorochrome channels...
Estimating linear transformation for scatter channels : reference marker = BV785 - CD3...
applying specific linear transformation for FSC-A channel...
initial quantiles : q5 = 48809.1266 ; q95 = 182769.1664
target quantiles : q5 = 0.3996 ; q95 = 2.9603
a = 1.91e-05 ; b = -5.33e-01
applying FSC-A linear transformation for FSC-H channel...
applying specific linear transformation for SSC-A channel...
initial quantiles : q5 = 41296.8164 ; q95 = 223620.1273
target quantiles : q5 = 0.3996 ; q95 = 2.9603
a = 1.40e-05 ; b = -1.80e-01
applying SSC-A linear transformation for SSC-H channel...

  |                                                                            
  |                                                                      |   0%
  |                                                                            
  |===================================                                   |  50%
  |                                                                            
  |======================================================================| 100%

#####################################################
### 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!
#####################################################
### running SCALE TRANSFORMATION processing steps ###
#####################################################
Proceeding with step 1 [flowframe_read] ...
#####################################################
### NOW PRE-PROCESSING FILE /Library/Frameworks/R.framework/Versions/4.3-x86_64/Resources/library/CytoPipeline/extdata/Donor1.fcs...
#####################################################
#####################################################
### NOW PRE-PROCESSING FILE /Library/Frameworks/R.framework/Versions/4.3-x86_64/Resources/library/CytoPipeline/extdata/Donor2.fcs...
#####################################################
#####################################################
### running SCALE TRANSFORMATION processing steps ###
#####################################################
Proceeding with step 1 [flowframe_read]: found in cache!
#####################################################
### NOW PRE-PROCESSING FILE /Library/Frameworks/R.framework/Versions/4.3-x86_64/Resources/library/CytoPipeline/extdata/Donor1.fcs...
#####################################################
Proceeding with step 1 [flowframe_read] ...
#####################################################
### NOW PRE-PROCESSING FILE /Library/Frameworks/R.framework/Versions/4.3-x86_64/Resources/library/CytoPipeline/extdata/Donor2.fcs...
#####################################################
Proceeding with step 1 [flowframe_read] ...
#####################################################
### running SCALE TRANSFORMATION processing steps ###
#####################################################
Proceeding with step 1 [flowframe_read]: found in cache!
#####################################################
### NOW PRE-PROCESSING FILE /Library/Frameworks/R.framework/Versions/4.3-x86_64/Resources/library/CytoPipeline/extdata/Donor1.fcs...
#####################################################
Proceeding with step 1 [flowframe_read]: found in cache!
Proceeding with step 2 [remove_margins] ...
Removing margins from file : Donor1.fcs
#####################################################
### NOW PRE-PROCESSING FILE /Library/Frameworks/R.framework/Versions/4.3-x86_64/Resources/library/CytoPipeline/extdata/Donor2.fcs...
#####################################################
Proceeding with step 1 [flowframe_read]: found in cache!
Proceeding with step 2 [remove_margins] ...
Removing margins from file : Donor2.fcs
#####################################################
### running SCALE TRANSFORMATION processing steps ###
#####################################################
Proceeding with step 1 [flowframe_read] ...
#####################################################
### NOW PRE-PROCESSING FILE /Library/Frameworks/R.framework/Versions/4.3-x86_64/Resources/library/CytoPipeline/extdata/Donor2.fcs...
#####################################################
#####################################################
### running SCALE TRANSFORMATION processing steps ###
#####################################################
Proceeding with step 1 [flowframe_read]: found in cache!
#####################################################
### NOW PRE-PROCESSING FILE /Library/Frameworks/R.framework/Versions/4.3-x86_64/Resources/library/CytoPipeline/extdata/Donor2.fcs...
#####################################################
Proceeding with step 1 [flowframe_read] ...
#####################################################
### running SCALE TRANSFORMATION processing steps ###
#####################################################
Proceeding with step 1 [flowframe_read]: found in cache!
#####################################################
### NOW PRE-PROCESSING FILE /Library/Frameworks/R.framework/Versions/4.3-x86_64/Resources/library/CytoPipeline/extdata/Donor2.fcs...
#####################################################
Proceeding with step 1 [flowframe_read]: found in cache!
Proceeding with step 2 [remove_margins] ...
Removing margins from file : Donor2.fcs
no sample file passed as argument => defaulting to first sample file
#####################################################
### running SCALE TRANSFORMATION processing steps ###
#####################################################
Proceeding with step 1 [flowframe_read]: found in cache!
#####################################################
### NOW PRE-PROCESSING FILE /Library/Frameworks/R.framework/Versions/4.3-x86_64/Resources/library/CytoPipeline/extdata/Donor1.fcs...
#####################################################
Proceeding with step 1 [flowframe_read] ...
Proceeding with step 2 [remove_margins] ...
Removing margins from file : Donor1.fcs
#####################################################
### NOW PRE-PROCESSING FILE /Library/Frameworks/R.framework/Versions/4.3-x86_64/Resources/library/CytoPipeline/extdata/Donor2.fcs...
#####################################################
Proceeding with step 1 [flowframe_read]: found in cache!
Proceeding with step 2 [remove_margins]: found in cache!
no sample file passed as argument => defaulting to first sample file
Object of class "CytoProcessingStep"
 Name: summing step
 Function: user-provided function
Compensating file : Donor1.fcs
Compensating file : Donor1.fcs
Removing margins from file : Donor1.fcs
Removing margins from file : Donor1.fcs
Removing margins from file : Donor1.fcs
Removing margins from file : Donor1.fcs
Compensating file : Donor1.fcs
Compensating file : Donor1.fcs
Compensating file : Donor2.fcs
Compensating file : Donor1.fcs
Compensating file : Donor1.fcs
Compensating file : Donor1.fcs
Applying PeacoQC method...
Starting quality control analysis for Donor1.fcs
Calculating peaks

  |                                                        
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  |++                                                |   5%
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  |+++++                                             |  10%
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  |++++++++                                          |  15%
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  |++++++++++                                        |  20%
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  |++++++++++++                                      |  25%
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  |+++++++++++++++                                   |  30%
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  |++++++++++++++++++                                |  35%
  |                                                        
  |++++++++++++++++++++                              |  40%
  |                                                        
  |++++++++++++++++++++++                            |  45%
  |                                                        
  |+++++++++++++++++++++++++                         |  50%
  |                                                        
  |++++++++++++++++++++++++++++                      |  55%
  |                                                        
  |++++++++++++++++++++++++++++++                    |  60%
  |                                                        
  |++++++++++++++++++++++++++++++++                  |  65%
  |                                                        
  |+++++++++++++++++++++++++++++++++++               |  70%
  |                                                        
  |++++++++++++++++++++++++++++++++++++++            |  75%
  |                                                        
  |++++++++++++++++++++++++++++++++++++++++          |  80%
  |                                                        
  |++++++++++++++++++++++++++++++++++++++++++        |  85%
  |                                                        
  |+++++++++++++++++++++++++++++++++++++++++++++     |  90%
  |                                                        
  |++++++++++++++++++++++++++++++++++++++++++++++++  |  95%
  |                                                        
  |++++++++++++++++++++++++++++++++++++++++++++++++++| 100%
Applying flowAI method...
Quality control for the file: Donor1
0% of anomalous cells detected in the flow rate check. 
0% of anomalous cells detected in signal acquisition check. 
3% of anomalous cells detected in the dynamic range check. 
[ FAIL 0 | WARN 0 | SKIP 3 | PASS 213 ]

══ Skipped tests (3) ═══════════════════════════════════════════════════════════
• On CRAN (3): 'test-ggplots.R:68:5', 'test-ggplots.R:185:5',
  'test-ggplots.R:310:5'

[ FAIL 0 | WARN 0 | SKIP 3 | PASS 213 ]
Deleting unused snapshots:
• ggplots/ggplotevents-1d-fill-and-color.svg
• ggplots/ggplotevents-1d-linear-double.svg
• ggplots/ggplotevents-1d-linear-explicit-range-single.svg
• ggplots/ggplotevents-1d-logicle-single.svg
• ggplots/ggplotevents-1d-logicle-with-explicit-params-single.svg
• ggplots/ggplotevents-1d-sub-sampling.svg
• ggplots/ggplotevents-1d-transformlist-linear-not-run.svg
• ggplots/ggplotevents-1d-transformlist-linear-run.svg
• ggplots/ggplotevents-1d-transformlist-logicle-not-run.svg
• ggplots/ggplotevents-1d-transformlist-logicle-run.svg
• ggplots/ggplotevents-2d-x-linear-y-logicle.svg
• ggplots/ggplotevents-2d-x-logicle-y-linear.svg
• ggplots/ggplotevents-2d-x-logicle-y-logicle-bins.svg
• ggplots/ggplotevents-2d-x-logicle-y-logicle-by-markers.svg
• ggplots/ggplotevents-2d-x-logicle-y-logicle-translist-not-run.svg
• ggplots/ggplotevents-2d-x-logicle-y-logicle-translist-run.svg
• ggplots/ggplotfilterevents-2d-5000-points.svg
• ggplots/ggplotfilterevents-2d-all-points-interactive.svg
• ggplots/ggplotfilterevents-2d-infinite-nb-of-points.svg
• ggplots/ggplotfilterevents-2d-small-size.svg
• ggplots/ggplotfilterevents-2d-translist-not-run.svg
• ggplots/ggplotfilterevents-2d-translist-run.svg
> 
> proc.time()
   user  system elapsed 
127.561   6.435 202.182 

Example timings

CytoPipeline.Rcheck/CytoPipeline-Ex.timings

nameusersystemelapsed
CytoPipelineClass0.0750.0110.120
CytoProcessingStep0.0070.0010.013
aggregateAndSample0.3660.0200.527
appendCellID0.2380.0130.336
applyScaleTransforms0.4600.0160.641
areFluoCols0.2420.0160.352
areSignalCols0.2250.0140.322
compensateFromMatrix2.7460.0933.913
computeScatterChannelsLinearScale0.3390.0150.484
estimateScaleTransforms0.3650.0120.513
execute47.570 2.67071.406
exportCytoPipeline0.0290.0030.036
findTimeChannel0.2120.0130.296
getAcquiredCompensationMatrix0.1480.0060.213
getChannelNamesFromMarkers0.2250.0140.320
getFCSFileName0.2160.0060.306
getTransfoParams0.2410.0090.332
ggplotEvents 9.138 0.16412.896
ggplotFilterEvents1.3280.0481.839
ggplotFlowRate1.9880.0292.757
handlingProcessingSteps0.0110.0050.022
inspectCytoPipelineObjects17.251 0.88224.782
interactingWithCytoPipelineCache25.267 1.30535.922
qualityControlFlowAI6.4960.4108.836
qualityControlPeacoQC1.5570.0412.100
readRDSObject0.4130.0120.541
readSampleFiles0.1860.0080.250
removeChannels0.2220.0090.309
removeDeadCellsManualGate0.2250.0070.290
removeDebrisManualGate0.2290.0070.305
removeDoubletsCytoPipeline0.2670.0100.360
removeMarginsPeacoQC0.5270.0260.720
runCompensation0.2660.0160.355
singletsGate1.7480.0612.274
subsample0.2240.0130.310
updateMarkerName0.2210.0130.302
writeFlowFrame0.4720.0290.713