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nextflow_schema.json
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715 lines (715 loc) · 32.1 KB
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{
"$schema": "https://json-schema.org/draft/2020-12/schema",
"$id": "https://raw.githubusercontent.com/nf-core/sopa/master/nextflow_schema.json",
"title": "nf-core/sopa pipeline parameters",
"description": "Technology-invariant pipeline for spatial omics analysis that scales to millions of cells",
"type": "object",
"$defs": {
"input_output_options": {
"title": "Input/output options",
"type": "object",
"fa_icon": "fas fa-terminal",
"description": "Define where the pipeline should find input data and save output data.",
"required": ["input", "outdir"],
"properties": {
"input": {
"type": "string",
"format": "file-path",
"exists": true,
"schema": "assets/schema_input.json",
"mimetype": "text/csv",
"pattern": "^\\S+\\.csv$",
"description": "Path to comma-separated file containing information about the samples in the experiment.",
"help_text": "You will need to create a design file with information about the samples in your experiment before running the pipeline. Use this parameter to specify its location. It has to be a comma-separated file with 3 columns, and a header row. See [usage docs](https://nf-co.re/sopa/usage#samplesheet-input).",
"fa_icon": "fas fa-file-csv"
},
"outdir": {
"type": "string",
"format": "directory-path",
"description": "The output directory where the results will be saved. You have to use absolute paths to storage on Cloud infrastructure.",
"fa_icon": "fas fa-folder-open"
},
"email": {
"type": "string",
"description": "Email address for completion summary.",
"fa_icon": "fas fa-envelope",
"help_text": "Set this parameter to your e-mail address to get a summary e-mail with details of the run sent to you when the workflow exits. If set in your user config file (`~/.nextflow/config`) then you don't need to specify this on the command line for every run.",
"pattern": "^([a-zA-Z0-9_\\-\\.]+)@([a-zA-Z0-9_\\-\\.]+)\\.([a-zA-Z]{2,5})$"
}
}
},
"spaceranger_options": {
"title": "Space Ranger options",
"type": "object",
"fa_icon": "fas fa-rocket",
"description": "Options related to Space Ranger execution and raw spatial data processing",
"properties": {
"spaceranger_probeset": {
"type": "string",
"format": "file-path",
"mimetype": "text/csv",
"pattern": "^\\S+\\.csv$",
"description": "Location of Space Ranger probeset file.",
"fa_icon": "fas fa-file-csv",
"exists": true
},
"spaceranger_reference": {
"type": "string",
"format": "path",
"description": "Location of Space Ranger reference directory. May be packed as `tar.gz` file.",
"help_text": "Please see the [10x website](https://support.10xgenomics.com/spatial-gene-expression/software/downloads/latest) to download either of the supported human or mouse references. If not specified the GRCh38 human reference is automatically downladed and used.",
"fa_icon": "fas fa-folder-open",
"default": "https://cf.10xgenomics.com/supp/spatial-exp/refdata-gex-GRCh38-2020-A.tar.gz",
"exists": true
}
}
},
"institutional_config_options": {
"title": "Institutional config options",
"type": "object",
"fa_icon": "fas fa-university",
"description": "Parameters used to describe centralised config profiles. These should not be edited.",
"help_text": "The centralised nf-core configuration profiles use a handful of pipeline parameters to describe themselves. This information is then printed to the Nextflow log when you run a pipeline. You should not need to change these values when you run a pipeline.",
"properties": {
"custom_config_version": {
"type": "string",
"description": "Git commit id for Institutional configs.",
"default": "master",
"hidden": true,
"fa_icon": "fas fa-users-cog"
},
"custom_config_base": {
"type": "string",
"description": "Base directory for Institutional configs.",
"default": "https://raw.githubusercontent.com/nf-core/configs/master",
"hidden": true,
"help_text": "If you're running offline, Nextflow will not be able to fetch the institutional config files from the internet. If you don't need them, then this is not a problem. If you do need them, you should download the files from the repo and tell Nextflow where to find them with this parameter.",
"fa_icon": "fas fa-users-cog"
},
"config_profile_name": {
"type": "string",
"description": "Institutional config name.",
"hidden": true,
"fa_icon": "fas fa-users-cog"
},
"config_profile_description": {
"type": "string",
"description": "Institutional config description.",
"hidden": true,
"fa_icon": "fas fa-users-cog"
},
"config_profile_contact": {
"type": "string",
"description": "Institutional config contact information.",
"hidden": true,
"fa_icon": "fas fa-users-cog"
},
"config_profile_url": {
"type": "string",
"description": "Institutional config URL link.",
"hidden": true,
"fa_icon": "fas fa-users-cog"
}
}
},
"generic_options": {
"title": "Generic options",
"type": "object",
"fa_icon": "fas fa-file-import",
"description": "Less common options for the pipeline, typically set in a config file.",
"help_text": "These options are common to all nf-core pipelines and allow you to customise some of the core preferences for how the pipeline runs.\n\nTypically these options would be set in a Nextflow config file loaded for all pipeline runs, such as `~/.nextflow/config`.",
"properties": {
"version": {
"type": "boolean",
"description": "Display version and exit.",
"fa_icon": "fas fa-question-circle",
"hidden": true
},
"publish_dir_mode": {
"type": "string",
"default": "copy",
"description": "Method used to save pipeline results to output directory.",
"help_text": "The Nextflow `publishDir` option specifies which intermediate files should be saved to the output directory. This option tells the pipeline what method should be used to move these files. See [Nextflow docs](https://www.nextflow.io/docs/latest/process.html#publishdir) for details.",
"fa_icon": "fas fa-copy",
"enum": ["symlink", "rellink", "link", "copy", "copyNoFollow", "move"],
"hidden": true
},
"email_on_fail": {
"type": "string",
"description": "Email address for completion summary, only when pipeline fails.",
"fa_icon": "fas fa-exclamation-triangle",
"pattern": "^([a-zA-Z0-9_\\-\\.]+)@([a-zA-Z0-9_\\-\\.]+)\\.([a-zA-Z]{2,5})$",
"help_text": "An email address to send a summary email to when the pipeline is completed - ONLY sent if the pipeline does not exit successfully.",
"hidden": true
},
"plaintext_email": {
"type": "boolean",
"description": "Send plain-text email instead of HTML.",
"fa_icon": "fas fa-remove-format",
"hidden": true
},
"monochrome_logs": {
"type": "boolean",
"description": "Do not use coloured log outputs.",
"fa_icon": "fas fa-palette",
"hidden": true
},
"hook_url": {
"type": "string",
"description": "Incoming hook URL for messaging service",
"fa_icon": "fas fa-people-group",
"help_text": "Incoming hook URL for messaging service. Currently, MS Teams and Slack are supported.",
"hidden": true
},
"validate_params": {
"type": "boolean",
"description": "Boolean whether to validate parameters against the schema at runtime",
"default": true,
"fa_icon": "fas fa-check-square",
"hidden": true
},
"pipelines_testdata_base_path": {
"type": "string",
"fa_icon": "far fa-check-circle",
"description": "Base URL or local path to location of pipeline test dataset files",
"default": "https://raw.githubusercontent.com/nf-core/test-datasets/",
"hidden": true
},
"trace_report_suffix": {
"type": "string",
"fa_icon": "far calendar",
"description": "Suffix to add to the trace report filename. Default is the date and time in the format yyyy-MM-dd_HH-mm-ss.",
"hidden": true
},
"help": {
"type": ["boolean", "string"],
"description": "Display the help message."
},
"help_full": {
"type": "boolean",
"description": "Display the full detailed help message."
},
"show_hidden": {
"type": "boolean",
"description": "Display hidden parameters in the help message (only works when --help or --help_full are provided)."
}
}
},
"reader": {
"title": "Reader",
"type": "object",
"description": "Parameters related to the SpatialData reader",
"default": "",
"properties": {
"technology": {
"type": "string",
"description": "Technology used for the spatial data, e.g., 'xenium', 'merscope', ...",
"enum": [
"xenium",
"merscope",
"cosmx",
"visium_hd",
"molecular_cartography",
"macsima",
"phenocycler",
"hyperion",
"ome_tif",
"toy_dataset"
],
"default": "xenium"
},
"visium_hd_imread_page": {
"type": "number",
"description": "Optional page for the imageio reader"
}
},
"required": ["technology"],
"fa_icon": "fas fa-arrows-alt-h"
},
"patches": {
"title": "Patches",
"type": "object",
"description": "Creation of the image and transcript patches before segmentation",
"default": "",
"properties": {
"patch_width_pixel": {
"type": "number",
"description": "Width (and height) of each patch in pixels"
},
"patch_overlap_pixel": {
"type": "number",
"description": "Number of overlapping pixels between the patches. We advise to choose approximately twice the diameter of a cell"
},
"patch_width_microns": {
"type": "number",
"description": "Width (and height) of each patch in microns"
},
"patch_overlap_microns": {
"type": "number",
"description": "Number of overlapping microns between the patches. We advise to choose approximately twice the diameter of a cell"
},
"prior_shapes_key": {
"type": "string",
"description": "Optional name of the boundaries element to use as a segmentation prior. Either a column name for the transcript dataframe, or a key of `sdata` containing the shapes names. If combining cellpose with proseg/baysor/comseg, it will be set automatically to `'cellpose_boundaries'`."
},
"unassigned_value": {
"type": "string",
"description": "If `prior_shapes_key` is provided, this is the value given to transcripts that are not inside any cell (if it's already 0, don't provide this argument)"
}
},
"fa_icon": "far fa-square"
},
"tissue_segmentation": {
"title": "Tissue segmentation",
"type": "object",
"description": "Parameters related to the tissue segmentation",
"default": "",
"properties": {
"use_tissue_segmentation": {
"type": "boolean",
"description": "Whether to run tissue segmentation"
},
"level": {
"type": "number",
"description": "Level of the image pyramid to use for tissue segmentation"
},
"mode": {
"type": "string",
"description": "Mode for the tissue segmentation: 'staining' or 'saturation' (for H&E images).",
"enum": ["staining", "saturation"]
},
"tissue_segmentation_kwargs": {
"type": "string",
"description": "Additional tissue segmentation parameters as a python dict string"
}
},
"fa_icon": "fab fa-bitbucket"
},
"filtering": {
"title": "Cell filtering",
"type": "object",
"description": "Filtering low-quality cells during and after segmentation",
"default": "",
"properties": {
"min_area_pixels2": {
"type": "number",
"description": "Cells with an area less than this value will be filtered. The unit is in pixels^2, and used by Stardist/Cellpose.",
"default": 0.0
},
"min_area_microns2": {
"type": "number",
"description": "Cells with an area less than this value will be filtered. The unit is in microns^2, and used by Baysor/Comseg. Not used by Proseg.",
"default": 0.0
},
"min_transcripts": {
"type": "number",
"description": "Cells with less transcripts than this value will be filtered."
},
"min_intensity_ratio": {
"type": "number",
"description": "Cells whose mean channel intensity is less than `min_intensity_ratio * quantile_90` will be filtered."
}
},
"fa_icon": "fas fa-filter"
},
"aggregation": {
"title": "Aggregation",
"type": "object",
"description": "Aggregation of genes and channels inside each cell",
"default": "",
"properties": {
"aggregate_genes": {
"type": "boolean",
"description": "Whether to aggregate the genes (counts) inside each cell"
},
"aggregate_channels": {
"type": "boolean",
"description": "Whether to aggregate the channels (intensity) inside each cell"
},
"expand_radius_ratio": {
"type": "string",
"description": "Cells polygons will be expanded by `expand_radius_ratio * mean_radius` for channels averaging **only**. This help better aggregate boundary stainings"
}
},
"fa_icon": "fas fa-calculator"
},
"scanpy_preprocessing": {
"title": "Scanpy preprocessing",
"type": "object",
"description": "Optional scanpy table preprocessing (log1p, UMAP, leiden clustering) after aggregation/annotation.",
"default": "",
"properties": {
"use_scanpy_preprocessing": {
"type": "boolean",
"description": "Whether to run scanpy preprocessing"
},
"resolution": {
"type": "number",
"description": "Resolution parameter for the leiden clustering"
},
"check_counts": {
"type": "boolean",
"description": "Whether to check that adata.X contains counts"
},
"hvg": {
"type": "boolean",
"description": "Whether to compute highly variable genes before computing the UMAP and clustering"
}
},
"fa_icon": "fas fa-tools"
},
"explorer": {
"title": "Explorer",
"type": "object",
"description": "Parameters related to the Xenium Explorer visualization tool",
"default": "",
"properties": {
"pixel_size": {
"type": "number",
"default": 0.2125,
"description": "Number of microns in a pixel. Invalid value can lead to inconsistent scales in the Explorer."
},
"lazy": {
"type": "boolean",
"default": true,
"description": "If `True`, will not load the full images in memory (except if the image memory is below `ram_threshold_gb`)"
},
"ram_threshold_gb": {
"type": "number",
"description": "Threshold (in gygabytes) from which image can be loaded in memory.",
"default": 4.0
}
},
"fa_icon": "fas fa-tools"
},
"image_preprocessing": {
"title": "Image preprocessing",
"type": "object",
"description": "Image preprocessing applied before channel-based segmentation methods (cellpose, stardist)",
"default": "",
"properties": {
"gaussian_sigma": {
"type": "number",
"description": "Parameter for scipy gaussian_filter (applied before running the segmentation method)"
},
"clip_limit": {
"type": "number",
"description": "Parameter for skimage.exposure.equalize_adapthist (applied before running the segmentation method)"
},
"clahe_kernel_size": {
"type": "number",
"description": "Parameter for skimage.exposure.equalize_adapthist (applied before running the segmentation method)"
}
},
"fa_icon": "fas fa-file-image"
},
"proseg": {
"title": "Proseg",
"type": "object",
"description": "Parameters related to the proseg segmentation method",
"default": "",
"properties": {
"use_proseg": {
"type": "boolean",
"description": "Whether to run proseg segmentation"
},
"command_line_suffix": {
"type": "string",
"description": "String suffix to add to the proseg command line. This can be used to add extra parameters to the proseg command line."
},
"infer_presets": {
"type": "boolean",
"description": "Whether to infer the proseg presets based on the columns of the transcripts dataframe."
},
"visium_hd_prior_shapes_key": {
"type": "string",
"description": "**Only for Visium HD data.** Key of `sdata` containing the prior cell boundaries. If `'auto'`, use the latest performed segmentation (e.g., stardist or the 10X Genomics segmentation). If combining stardist with proseg, it will be set automatically to `'stardist_boundaries'`."
}
},
"fa_icon": "fas fa-tools"
},
"comseg": {
"title": "Comseg",
"type": "object",
"description": "Parameters related to the comseg segmentation method",
"default": "",
"properties": {
"use_comseg": {
"type": "boolean",
"description": "Whether to run comseg segmentation"
},
"mean_cell_diameter": {
"type": "number",
"description": "Comseg `mean_cell_diameter` parameter",
"default": 10.0
},
"max_cell_radius": {
"type": "number",
"description": "Comseg `max_cell_radius` parameter",
"default": 15.0
},
"alpha": {
"type": "number",
"description": "Comseg `alpha` parameter",
"default": 0.5
},
"min_rna_per_cell": {
"type": "number",
"description": "Comseg `min_rna_per_cell` parameter",
"default": 1.0
},
"allow_disconnected_polygon": {
"type": "boolean",
"description": "Comseg `allow_disconnected_polygon` parameter"
},
"norm_vector": {
"type": "boolean",
"description": "Comseg `norm_vector` parameter"
}
},
"fa_icon": "fas fa-tools"
},
"baysor": {
"title": "Baysor",
"type": "object",
"description": "Parameters related to the baysor segmentation method",
"default": "",
"properties": {
"use_baysor": {
"type": "boolean",
"description": "Whether to run baysor segmentation"
},
"baysor_scale": {
"type": "number",
"description": "Baysor `scale` parameter",
"default": -1.0
},
"baysor_scale_std": {
"type": "string",
"description": "Baysor `scale_std` parameter",
"default": "25%"
},
"prior_segmentation_confidence": {
"type": "number",
"description": "Baysor `prior_segmentation_confidence` parameter",
"default": 0.2
},
"min_molecules_per_cell": {
"type": "number",
"description": "Baysor `min_molecules_per_cell` parameter",
"default": 20.0
},
"min_molecules_per_gene": {
"type": "number",
"description": "Baysor `min_molecules_per_gene` parameter",
"default": 10.0
},
"min_molecules_per_segment": {
"type": "number",
"description": "Baysor `min_molecules_per_segment` parameter"
},
"confidence_nn_id": {
"type": "number",
"description": "Baysor `confidence_nn_id` parameter"
},
"force_2d": {
"type": "boolean",
"description": "Baysor `force_2d` parameter",
"default": true
}
},
"fa_icon": "fas fa-tools"
},
"cellpose": {
"title": "Cellpose",
"type": "object",
"description": "Parameters related to the cellpose segmentation method",
"default": "",
"properties": {
"use_cellpose": {
"type": "boolean",
"description": "Whether to run cellpose segmentation"
},
"cellpose_diameter": {
"type": "number",
"description": "Cellpose `diameter` parameter"
},
"cellpose_channels": {
"type": "string",
"description": "Channel name(s) to use for cellpose segmentation. If multiple, separate by space, comma or pipe characters."
},
"flow_threshold": {
"type": "number",
"description": "Cellpose `flow_threshold` parameter"
},
"cellprob_threshold": {
"type": "number",
"description": "Cellpose `cellprob_threshold` parameter"
},
"cellpose_model_type": {
"type": "string",
"description": "Cellpose model type to use"
},
"pretrained_model": {
"type": "string",
"description": "Cellpose `pretrained_model` parameter"
},
"cellpose_use_gpu": {
"type": "boolean",
"description": "Whether to use GPU for Cellpose segmentation"
},
"cellpose_kwargs": {
"type": "string",
"description": "Additional cellpose parameters as a python dict string"
}
},
"fa_icon": "fas fa-tools"
},
"stardist": {
"title": "Stardist",
"type": "object",
"description": "Parameters related to the stardist segmentation method",
"default": "",
"properties": {
"use_stardist": {
"type": "boolean",
"description": "Whether to run stardist segmentation"
},
"stardist_model_type": {
"type": "string",
"description": "Name of stardist model to use"
},
"prob_thresh": {
"type": "number",
"description": "Stardist `prob_thresh` parameter"
},
"nms_thresh": {
"type": "number",
"description": "Stardist `nms_thresh` parameter"
},
"stardist_channels": {
"type": "string",
"description": "Optional channel name(s) to use for stardist segmentation. If multiple, separate by space, comma or pipe characters."
},
"stardist_kwargs": {
"type": "string",
"description": "Additional stardist parameters as a python dict string"
}
},
"fa_icon": "fas fa-tools"
},
"tangram": {
"title": "Tangram",
"type": "object",
"description": "Parameters related to the tangram cell-type annotation method",
"default": "",
"properties": {
"use_tangram": {
"type": "boolean",
"description": "Whether to run tangram cell-type annotation"
},
"sc_reference_path": {
"type": "string",
"description": "Path to the scRNAseq annotated reference, as a `.h5ad` file"
},
"tangram_cell_type_key": {
"type": "string",
"description": "Key of `adata_ref.obs` containing the cell-types"
},
"reference_preprocessing": {
"type": "string",
"description": "Preprocessing method applied to the reference. Either None (raw counts), or `normalized` (sc.pp.normalize_total) or `log1p` (sc.pp.normalize_total and sc.pp.log1p)"
},
"bag_size": {
"type": "number",
"description": "Number of cells in each bag of the spatial table. Low values will decrease the memory usage"
},
"max_obs_reference": {
"type": "number",
"description": "Maximum samples to be considered in the reference for tangram. Low values will decrease the memory usage"
}
},
"fa_icon": "fas fa-scroll"
},
"fluorescence_annotation": {
"title": "Fluorescence annotation",
"type": "object",
"description": "Parameters related to the fluorescence-based cell-type annotation method",
"default": "",
"properties": {
"use_fluorescence_annotation": {
"type": "boolean",
"description": "Whether to run cell-type annotation based on a marker-to-cell dictionary"
},
"fluorescence_cell_type_key": {
"type": "string",
"description": "Key of `sdata.obs` containing the cell-types"
},
"marker_cell_dict": {
"type": "string",
"description": "Dictionary mapping whose keys are marker channel names and values are the cell types associated to each marker. Should be provided as a string representation of a python dictionary."
}
},
"fa_icon": "fas fa-scroll"
}
},
"allOf": [
{
"$ref": "#/$defs/input_output_options"
},
{
"$ref": "#/$defs/spaceranger_options"
},
{
"$ref": "#/$defs/institutional_config_options"
},
{
"$ref": "#/$defs/generic_options"
},
{
"$ref": "#/$defs/reader"
},
{
"$ref": "#/$defs/patches"
},
{
"$ref": "#/$defs/tissue_segmentation"
},
{
"$ref": "#/$defs/filtering"
},
{
"$ref": "#/$defs/aggregation"
},
{
"$ref": "#/$defs/scanpy_preprocessing"
},
{
"$ref": "#/$defs/explorer"
},
{
"$ref": "#/$defs/image_preprocessing"
},
{
"$ref": "#/$defs/proseg"
},
{
"$ref": "#/$defs/comseg"
},
{
"$ref": "#/$defs/baysor"
},
{
"$ref": "#/$defs/cellpose"
},
{
"$ref": "#/$defs/stardist"
},
{
"$ref": "#/$defs/tangram"
},
{
"$ref": "#/$defs/fluorescence_annotation"
}
]
}