Description Usage Arguments Value
Wrapper to the Infinity Flow pipeline
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 | infinity_flow(
path_to_fcs,
path_to_output,
path_to_intermediary_results = tempdir(),
backbone_selection_file = NULL,
annotation = NULL,
isotype = NULL,
input_events_downsampling = Inf,
prediction_events_downsampling = 1000,
cores = 1L,
your_random_seed = 123,
verbose = TRUE,
extra_args_read_FCS = list(emptyValue = FALSE, truncate_max_range = FALSE,
ignore.text.offset = TRUE),
regression_functions = list(XGBoost = fitter_xgboost),
extra_args_regression_params = list(list(nrounds = 500, eta = 0.05)),
extra_args_UMAP = list(n_neighbors = 15L, min_dist = 0.2, metric = "euclidean",
verbose = verbose, n_epochs = 1000L, n_threads = cores, n_sgd_threads = cores),
extra_args_export = list(FCS_export = c("split", "concatenated", "none")[1],
CSV_export = FALSE),
extra_args_correct_background = list(FCS_export = c("split", "concatenated",
"none")[1], CSV_export = FALSE),
extra_args_plotting = list(chop_quantiles = 0.005),
neural_networks_seed = NULL
)
|
path_to_fcs |
Path to the input directory where input FCS files are stored (one file per well). Will look for FCS files recursively in that directory. |
path_to_output |
Path to the output directory where final results will be stored |
path_to_intermediary_results |
Path to results to store temporary data. If left blank, will default to a temporary directory. It may be useful to store the intermediary results to further explore the data, tweak the pipeline or to resume computations. |
backbone_selection_file |
If that argument is missing and R is run interactively, the user will be prompted to state whether each channel in the FCS file should be considered backbone measurement, exploratory measurement or ignored. Otherwise, the user should run |
annotation |
Named character vector. Elements should be the targets of the exploratory antibodies, names should be the name of the FCS file where that exploratory antibody was measured. |
isotype |
Named character vector. Elements should be the isotype used in each of the well and that (e.g. IgG2). The corresponding isotype should be present in annotation (e.g. Isotype_IgG2, with this capitalization exactly). Autofluorescence measurements should be listed here as "Blank" |
input_events_downsampling |
How many event should be kept per input FCS file. Default to no downsampling. In any case, half of the events will be used to train regression models and half to test the performance. Predictions will be made only on events from the test set, and downsampled according to prediction_events_downsampling. |
prediction_events_downsampling |
How many event should be kept per input FCS file to output prediction for. Default to 1000. |
cores |
Number of cores to use for parallel computing. Defaults to 1 (no parallel computing) |
your_random_seed |
Deprecated: was used to set a seed for computationally reproducible results but is not allowed by Bioconductor. Please set a random seed yourself using set.seed(somenumber) if you desire computionally-reproducible results. |
verbose |
Whether to print information about progress |
extra_args_read_FCS |
list of named arguments to pass to flowCore:read.FCS. Defaults to list(emptyValue=FALSE,truncate_max_range=FALSE,ignore.text.offset=TRUE) which in our experience avoided issues with data loading. |
regression_functions |
named list of fitter_* functions (see ls("package:infinityFlow") for the complete list). The names should be desired names for the different models. Each object of the list will correspond to a machine learning model to train. Defaults to list(XGBoost = fitter_xgboost). |
extra_args_regression_params |
list of lists the same length as the regression_functions argument. Each element should be a named list, that will be passed as named arguments to the corresponding fitter_ function. Defaults to list(list(nrounds = 500, eta = 0.05)). |
extra_args_UMAP |
list of named arguments to pass to uwot:umap. Defaults to list(n_neighbors=15L,min_dist=0.2,metric="euclidean",verbose=verbose,n_epochs=1000L) |
extra_args_export |
Whether raw imputed data should be exported. Possible values are list(FCS_export = "split") to export one FCS file per input well, list(FCS_export = "concatenated") to export a single concatenated FCS file containing all the dataset, list(FCS_export = "csv") for a single CSV file containing all the dataset. You can export multiple modalities by using for instance extra_args_export = list(FCS_export = c("split", "concatenated", "csv")) |
extra_args_correct_background |
Whether background-corrected imputed data should be exported. Possible values are list(FCS_export = "split") to export one FCS file per input well, list(FCS_export = "concatenated") to export a single concatenated FCS file containing all the dataset, list(FCS_export = "csv") for a single CSV file containing all the dataset. You can export multiple modalities by using for instance extra_args_export = list(FCS_export = c("split", "concatenated", "csv")) |
extra_args_plotting |
list of named arguments to pass to plot_results. Defaults to list(chop_quantiles=0.005) which removes the top 0.05% and bottom 0.05% of the scale for each marker when mapping color palettes to intensities. |
neural_networks_seed |
Seed for computationally reproducible results when using neural networks (in additional to the other sources of stochasticity - sampling - that are made reproducible by the your_random_seed argument. |
Raw and background-corrected imputed expression data for every Infinity antibody
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