parallel.invoke.gpxp | R Documentation |
This function is desgined launch the parallelization of the gpxp function in the mIFTO code. It is used to create a local environment with only necessary data for the cluster objects.
parallel.invoke.gpxp(
Concentration,
x,
y,
Image.IDs,
Antibody_Opal,
titration.type.name,
Thresholds,
paths,
connected.pixels,
flowout,
Opal1,
decile.logical,
threshold.logical,
cl
)
Concentration |
a numeric vector of concentrations used in the titration |
x |
a unique identifier for the slide to be analyzed |
y |
the numeric of which index from the concentration vector to use |
Image.IDs |
the image coordinates of the current image as a comma separated pair |
Antibody_Opal |
the paired string for an antibody opal pair, designated as "AB (Opal NNN)" |
titration.type.name |
the type of titration that was performed (TSA or Primary) |
Thresholds |
a list of thresholds used for each concentration and slide |
paths |
the paths to the data as a list, with an element for each concentration |
connected.pixels |
the number of pixels that a pixel must be connected to for positivity measures |
flowout |
logical for whether or not flow like results will be produced |
Opal1 |
the opal value of interest |
decile.logical |
whether or not to run a decile approach analysis |
threshold.logical |
whether or not to run a threshold approach analysis |
cl |
cluster object |
It is meant to be run through the RUN function
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