## Loading required package: flowWorkspaceData
The openCyto package is designed to facilitate the automated gating methods in sequential way to mimic the manual gating scheme.
Traditionally, scientists have to draw the gates for each individual sample on each 2D projections (2 channels) within
Or draw the 'template gate's on one sample and replicate it to other samples, then manually inspect the gate on each sample
to do the correction if necessary. Either way is time consuming and subjective, thus not suitable for the large data sets
generated by high-throughput flow Cytometers or the
cross-lab data analysis.
Here is one
xml workspace (manual gating scheme) exported from
flowDataPath <- system.file("extdata", package = "flowWorkspaceData") wsfile <- list.files(flowDataPath, pattern="manual.xml",full = TRUE) wsfile
##  "/home/biocbuild/bbs-3.6-bioc/R/library/flowWorkspaceData/extdata/manual.xml"
flowWorkspacepackage, We can load it into R,
ws <- openWorkspace(wsfile)
manual gatesdefined in
xmlto the raw
gs <- parseWorkspace(ws, name= "T-cell", subset =1, isNcdf = TRUE)
and then visualize the
gh <- gs[] plot(gh)
This is a gating scheme for
T cell panel, which tries to identify
T cell sub-populations.
We can achieve the same results by using automated gating pipeline provided by this package.
flowClust and other packages provides many different gating methods to
detect cell populations and draw the gates automatically.
flowWorkspace package provides the
GatingSet as an efficient data structure to store, query and visualize the hierarchical gated data.
By taking advantage of these tools,
openCyto package can create the automated gating pipeline by a
gating template, which is essentially the same kind of hierarchical gating scheme
used by the biologists and scientists.
First of all, we need to describe the gating hierarchy in a spread sheet (a plain text format). This spread sheet must have the following columns:
alias: a name used label the cell population, the path composed by the alias and its precedent nodes (e.g. /root/A/B/alias) has to be uniquely identifiable.
pop: population patterns of
+/-+/-, which tells the algorithm which side (postive or negative) of 1d gate or which quadrant of 2d gate to be kept.
parent: the parent population alias, its path has to be uniquely identifiable.
dims: characters seperated by comma specifying the dimensions(1d or 2d) used for gating. It can be either channel name or stained marker name.
gating_method: the name of the gating function (e.g.
flowClust). It is invoked by a wrapper function that has the identical function name prefixed with a dot.(e.g.
gating_args: the named arguments passed to gating function
collapseDataForGating: When TRUE, data is collapsed (within groups if
groupByspecified) before gating and the gate is replicated across collapsed samples. When set FALSE (or blank),then
groupByargument is only used by
preprocessingand ignored by gating.
groupBy: If given, samples are split into groups by the unique combinations of study variable (i.e. column names of pData,e.g.“PTID:VISITNO”). when split is numeric, then samples are grouped by every N samples
preprocessing_method: the name of the preprocessing function(e.g.
prior_flowClust). It is invoked by a wrapper function that has the identical function name prefixed with a dot.(e.g.
.prior_flowClust) the preprocessing results are then passed to gating wrapper function through
preprocessing_args: the named arguments passed to preprocessing function.
Here is the an example of the gating template.
library(openCyto) library(data.table) gtFile <- system.file("extdata/gating_template/tcell.csv", package = "openCyto") dtTemplate <- fread(gtFile, autostart = 1L) dtTemplate
## alias pop parent dims gating_method ## 1: nonDebris + root FSC-A mindensity ## 2: singlets + nonDebris FSC-A,FSC-H singletGate ## 3: lymph + singlets FSC-A,SSC-A flowClust ## 4: cd3 + lymph CD3 mindensity ## 5: * -/++/- cd3 cd4,cd8 mindensity ## 6: activated cd4 ++ cd4+cd8- CD38,HLA tailgate ## 7: activated cd8 ++ cd4-cd8+ CD38,HLA tailgate ## 8: CD45_neg - cd4+cd8- CD45RA mindensity ## 9: CCR7_gate + CD45_neg CCR7 flowClust ## 10: * +/-+/- cd4+cd8- CCR7,CD45RA refGate ## 11: * +/-+/- cd4-cd8+ CCR7,CD45RA mindensity ## gating_args collapseDataForGating groupBy ## 1: NA NA ## 2: NA NA ## 3: K=2,target=c(1e5,5e4) NA NA ## 4: TRUE 4 ## 5: gate_range=c(1,3) NA NA ## 6: NA NA ## 7: tol=0.08 NA NA ## 8: gate_range=c(2,3) NA NA ## 9: neg=1,pos=1 NA NA ## 10: CD45_neg:CCR7_gate NA NA ## 11: NA NA ## preprocessing_method preprocessing_args ## 1: NA ## 2: NA ## 3: prior_flowClust NA ## 4: NA ## 5: NA ## 6: standardize_flowset NA ## 7: standardize_flowset NA ## 8: NA ## 9: NA ## 10: NA ## 11: NA
Each row is usually corresponding to one cell population and the gating method that is used to get that population. We will try to explain how to create this gating template based on the manual gating scheme row by row.
## alias pop parent dims gating_method gating_args ## 1: nonDebris + root FSC-A mindensity ## collapseDataForGating groupBy preprocessing_method preprocessing_args ## 1: NA NA NA
root(which is always the first node of
gating hierarchyby default).
mindensity(one of the
gatingfunctions provided by
gating_methodto gate on dimension (
popfield indicates the
positiveside of 1d gate is kept as the population of interest.
preprocessinginvolved in this gate, thus leave the other columns as
## alias pop parent dims gating_method gating_args ## 1: singlets + nonDebris FSC-A,FSC-H singletGate ## collapseDataForGating groupBy preprocessing_method preprocessing_args ## 1: NA NA NA
singletGate(function from by
polygonGatewill be generated on
dims) for each sample.
popfield stands for
"singlets+". But here it is 2d gate, which means we want to keep the area inside of the polygon
## alias pop parent dims gating_method gating_args ## 1: lymph + singlets FSC-A,SSC-A flowClust K=2,target=c(1e5,5e4) ## collapseDataForGating groupBy preprocessing_method preprocessing_args ## 1: NA NA prior_flowClust NA
aliasspecifies the name of population
gating_methodto do the 2-dimensional gating,
dimsis comma separated string,
FSC-A) goes first,
SSC-A) the second. This order doesn't affect the gating process but will determine how the gates are displayed.
flowClustalgorithm accepts can be put in
gating-argsas if they are typed in
R console. see
help(flowClust)for more details of these arguments
flowClustalgorithm accept the extra arguments
priorsthat is calculated during
preprocessingstage (before the actual
gating), thus, we supply the
## alias pop parent dims gating_method gating_args collapseDataForGating ## 1: cd3 + lymph CD3 mindensity TRUE ## groupBy preprocessing_method preprocessing_args ## 1: 4 NA
It is similar to the
nonDebris gate except that we specify
which tells the pipeline to
collapse all samples into one and applies
mindensity to the collapsed data on
Once the gate is generated, it is replicated across all samples. This is only useful when each individual sample does not have
enough events to deduce the gate. Here we do this just for the purpose of proof of concept.
The forth row specifies
cd4+/-cd8+/-, which will be expanded this into 6 rows.
## alias pop parent dims gating_method gating_args ## 1: * -/++/- cd3 cd4,cd8 mindensity gate_range=c(1,3) ## collapseDataForGating groupBy preprocessing_method preprocessing_args ## 1: NA NA NA
First two rows are two 1d gates that will be generated by
gating_method on each
## alias pop parent dims gating_method ## 1: cd4+ + /nonDebris/singlets/lymph/cd3 cd4 mindensity ## 2: cd8+ + /nonDebris/singlets/lymph/cd3 cd8 mindensity ## gating_args collapseDataForGating groupBy preprocessing_method ## 1: gate_range=c(1,3) ## 2: gate_range=c(1,3) ## preprocessing_args ## 1: ## 2:
Then another 4 rows are 4
rectangleGates that corresponds to the 4
quadrants in 2d projection (
cd4 vs cd8).
## alias pop parent dims gating_method ## 1: cd4+cd8+ ++ /nonDebris/singlets/lymph/cd3 cd4,cd8 refGate ## 2: cd4-cd8+ -+ /nonDebris/singlets/lymph/cd3 cd4,cd8 refGate ## 3: cd4+cd8- +- /nonDebris/singlets/lymph/cd3 cd4,cd8 refGate ## 4: cd4-cd8- -- /nonDebris/singlets/lymph/cd3 cd4,cd8 refGate ## gating_args ## 1: /nonDebris/singlets/lymph/cd3/cd4+:/nonDebris/singlets/lymph/cd3/cd8+ ## 2: /nonDebris/singlets/lymph/cd3/cd4+:/nonDebris/singlets/lymph/cd3/cd8+ ## 3: /nonDebris/singlets/lymph/cd3/cd4+:/nonDebris/singlets/lymph/cd3/cd8+ ## 4: /nonDebris/singlets/lymph/cd3/cd4+:/nonDebris/singlets/lymph/cd3/cd8+ ## collapseDataForGating groupBy preprocessing_method preprocessing_args ## 1: ## 2: ## 3: ## 4:
As we see here,
gating_method indicates that they are constructed based on the
gate coordinates of the previous two 1d gates.
Those 1d gates are thus considered as
"reference gates" that are referred by colon separated
alias string in
Alternatively, we can expand it into these 6 rows explicitly in the spread sheet.
But this convenient representation is recommended unless user wants have finer control on how the gating is done.
For instance, sometime we need to use different
gating_methods to generate 1d gates on
cd8 gating needs to depend on
cd4 gating ,i.e. the
cd4-) instead of
Sometimes we want to have the customized
alias other than quadrant-like name (
x+y+) that gets generated automatically.
(e.g. 5th row of the gating template)
After the gating template is defined in the spread sheet, it can be loaded into R:
gt_tcell <- gatingTemplate(gtFile, autostart = 1L) gt_tcell
## --- Gating Template: default ## with 29 populations defined
Besides looking at the spread sheet, we can examine the gating scheme by visualizing it:
As we can see, the gating scheme has been expanded as we described above.
All the colored arrows source from the
parent population and the grey arrows source from the
Once we are satisfied with the gating template, we can apply it to the actual flow data.
First of all, we load the raw FCS files into R by
ncdfFlow::read.ncdfFlowSet (It uses less memory than
flowCore::read.flowSet) and create an empty
fcsFiles <- list.files(pattern = "CytoTrol", flowDataPath, full = TRUE) ncfs <- read.ncdfFlowSet(fcsFiles) fr <- ncfs[] gs <- GatingSet(ncfs) gs
## A GatingSet with 2 samples
Then, compensate the data. If we have compensation controls (i.e. single stained samples), we can calculate the
compensation matrix by
Here we simply use the compensation matrix defined in
compMat <- getCompensationMatrices(gh) gs <- compensate(gs, compMat)
Here is one example showing the compensation outcome:
All the stained channels need to be transformed properly before the gating.
Here we use the
flowCore::estimateLogicle to do the
chnls <- parameters(compMat) trans <- estimateLogicle(gs[], channels = chnls) gs <- transform(gs, trans)
Here is one example showing the transformation outcome:
Now we can apply the gating template to the data:
Optionally, we can run the pipeline in
parallel to speed up gating. e.g.
gating(gt_tcell, gs, mc.cores=2, parallel_type = "multicore")
After gating, there are some extra populations generated automatically by the pipeline (e.g.
We can hide these populations if we are not interested in them:
dodesToHide <- c("cd8+", "cd4+" , "cd4-cd8-", "cd4+cd8+" , "cd4+cd8-/HLA+", "cd4+cd8-/CD38+" , "cd4-cd8+/HLA+", "cd4-cd8+/CD38+" , "CD45_neg/CCR7_gate", "cd4+cd8-/CD45_neg" , "cd4-cd8+/CCR7+", "cd4-cd8+/CD45RA+" ) lapply(dodesToHide, function(thisNode)setNode(gs, thisNode, FALSE))
And rename the populations:
setNode(gs, "cd4+cd8-", "cd4") setNode(gs, "cd4-cd8+", "cd8")
Sometime it will be helpful (especially to work with an already gated data) to be able to interact with he GatingSet directly without the need to write the compelete csv gating template.
openCyto package allows user to specify their gating schemes and gate the data
in a data-driven fasion. It frees the scientists from the labor-intensitive manual gating routines
and increases the speed as well as the reproducibilty and objectivity of the data analysis work.