populate.tables | R Documentation |
This function is desgined to do analysis for IF titration series in Pixel by Pixel data provding output for each IMAGE individually grouped by Concentration
populate.tables(
Slide_Descript,
Concentration,
Antibody_Opal,
Thresholds,
Opal1,
flowout,
Protocol,
paths,
titration.type.name,
connected.pixels,
decile.logical,
threshold.logical,
pb.count,
pb.Object
)
Concentration |
a numeric vector of concentrations used in the titration |
Antibody_Opal |
the paired string for an antibody opal pair, designated as "AB (Opal NNN)" |
Thresholds |
a list of thresholds used for each concentration and slide |
Opal1 |
the opal value of interest |
flowout |
logical for whether or not flow like results will be produced (1 for produce, 0 for don't) |
Protocol |
the protocol type (7color or 9color) |
paths |
the data paths, one data path for each concentration |
titration.type.name |
the titration type for a given dilution set (Primary or TSA) |
connected.pixels |
the number of pixels that a pixel must be connected to for positivity measures |
decile.logical |
whether or not to run a decile approach analysis |
threshold.logical |
whether or not to run a threshold approach analysis |
pb.count |
current count for progress bar |
pb.Object |
progress bar object |
Slide_Desctipt |
a unique identifier for each slide to be analyzed |
It is meant to be run through the RUN function
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