Generate single-cell images ¶

Here, we are going to process the previously ingested microscopy images with the scPortrait pipeline to generate single-cell images that we can use to assess autophagosome formation at a single-cell level.

import lamindb as ln
from collections.abc import Iterable

from pathlib import Path
from scportrait.pipeline.extraction import HDF5CellExtraction
from scportrait.pipeline.project import Project
from scportrait.pipeline.segmentation.workflows import CytosolSegmentationCellpose

ln.track()

Query microscopy images¶

First, we query for the raw and annotated microscopy images.

input_images = ln.Artifact.filter(
    ulabels__name="autophagy imaging", description__icontains="raw image", suffix=".tif"
)

The experiment includes two genotypes (WT and EI24KO) under two treatment conditions (unstimulated vs. 14h Torin-1). Multiple clonal cell lines were imaged for each condition across several fields of view (FOVs) and imaging channels.

We’ll extract single-cell images from each FOV and annotate them with metadata including genotype, treatment condition, clonal cell line, and imaging experiment.

input_images_df = input_images.to_dataframe(features=True)

display(input_images_df.head())

conditions = input_images_df["stimulation"].unique().tolist()
cell_line_clones = input_images_df["cell_line_clone"].unique().tolist()
FOVs = input_images_df["FOV"].unique().tolist()

Show code cell output Hide code cell output

! truncated query result to limit=20 Artifact objects

/tmp/ipykernel_3303/1645869880.py:1: DeprecationWarning: `features=True` is deprecated, pass `include="features"` instead.
  input_images_df = input_images.to_dataframe(features=True)

	uid	key	genotype	stimulation	cell_line_clone	channel	FOV	magnification	microscope	imaged structure	resolution	study
id
49	AVRTVX9gEu4LrTAP0000	input_data_imaging_usecase/images/Timepoint001...	EI24KO	untreated	U2OS lcklip-mNeon mCherryLC3B EI24 KO clone 2	mCherry	FOV2	20X	Opera Phenix	mCherry-LC3B	0.597976	autophagy imaging
48	6uUjyphUD4D1Hixc0000	input_data_imaging_usecase/images/Timepoint001...	EI24KO	untreated	U2OS lcklip-mNeon mCherryLC3B EI24 KO clone 2	mCherry	FOV1	20X	Opera Phenix	mCherry-LC3B	0.597976	autophagy imaging
47	AhBvnNKg5yJcG6LU0000	input_data_imaging_usecase/images/Timepoint001...	EI24KO	untreated	U2OS lcklip-mNeon mCherryLC3B EI24 KO clone 2	DAPI	FOV2	20X	Opera Phenix	DNA	0.597976	autophagy imaging
46	Cvamog4G3a2XYGM80000	input_data_imaging_usecase/images/Timepoint001...	EI24KO	untreated	U2OS lcklip-mNeon mCherryLC3B EI24 KO clone 2	DAPI	FOV1	20X	Opera Phenix	DNA	0.597976	autophagy imaging
45	Oww4y0yYuR8pxV9q0000	input_data_imaging_usecase/images/Timepoint001...	EI24KO	untreated	U2OS lcklip-mNeon mCherryLC3B EI24 KO clone 2	Alexa488	FOV2	20X	Opera Phenix	LckLip-mNeon	0.597976	autophagy imaging

Alternatively, we can query for the ULabel directly:

conditions = ln.ULabel.filter(
    links_artifact__feature__name="stimulation", artifacts__in=input_images
).distinct()

cell_line_clones = ln.ULabel.filter(
    links_artifact__feature__name="cell_line_clone", artifacts__in=input_images
).distinct()

FOVs = ln.ULabel.filter(
    links_artifact__feature__name="FOV", artifacts__in=input_images
).distinct()

By iterating through conditions, cell lines and FOVs, we should only have 3 images showing a single FOV to enable processing using scPortrait.

# Create artifact type feature and associated label
ln.Feature(name="artifact type", dtype=ln.ULabel).save()
ln.ULabel(name="scportrait config").save()

# Load config file for processing all datasets
config_file_af = ln.Artifact.connect("scportrait/examples").get(
    key="input_data_imaging_usecase/config.yml"
)

config_file_af.description = (
    "config for scportrait for processing of cells stained for autophagy markers"
)
config_file_af.save()

# Annotate the config file with the metadata relevant to the study
config_file_af.features.add_values(
    {"study": "autophagy imaging", "artifact type": "scportrait config"}
)

Process images with scPortrait¶

Let’s take a look at the processing of one example FOV.

# Get input images for one example FOV
condition, cellline, FOV = conditions[0], cell_line_clones[0], FOVs[0]

images = (
    input_images.filter(ulabels=condition)
    .filter(ulabels=cellline)
    .filter(ulabels=FOV)
    .distinct()
)

# Quick sanity check - all images should share metadata except channel/structure
values_to_ignore = ["channel", "imaged structure"]
features = images.first().features.get_values()
shared_features = {k: v for k, v in features.items() if k not in values_to_ignore}

for image in images:
    image_features = image.features.get_values()
    filtered_features = {
        k: v for k, v in image_features.items() if k not in values_to_ignore
    }
    assert shared_features == filtered_features

# Get image paths in correct channel order
input_image_paths = [
    images.filter(ulabels__name=channel).one().cache()
    for channel in ["DAPI", "Alexa488", "mCherry"]
]

# Create output directory and unique project ID
output_directory = "processed_data"
unique_project_id = f"{shared_features['cell_line_clone']}/{shared_features['stimulation']}/{shared_features['FOV']}".replace(
    " ", "_"
)
project_location = f"{output_directory}/{unique_project_id}/scportrait_project"

# Create directories
Path(project_location).mkdir(parents=True, exist_ok=True)

# Initialize the scPortrait project
project = Project(
    project_location=project_location,
    config_path=config_file_af.cache(),
    segmentation_f=CytosolSegmentationCellpose,
    extraction_f=HDF5CellExtraction,
    overwrite=True,
)

# Load images and process
project.load_input_from_tif_files(
    input_image_paths, overwrite=True, channel_names=["DAPI", "Alexa488", "mCherry"]
)
project.segment()
project.extract()

Show code cell output Hide code cell output

Updating project config file.

/tmp/ipykernel_3303/1211438391.py:12: UserWarning: There is already a directory in the location path
  project = Project(

  0%|          | 0.00/25.3M [00:00<?, ?B/s]

  1%|          | 320k/25.3M [00:00<00:08, 3.09MB/s]

  6%|▌         | 1.41M/25.3M [00:00<00:03, 7.68MB/s]

 22%|██▏       | 5.59M/25.3M [00:00<00:00, 22.9MB/s]

 73%|███████▎  | 18.4M/25.3M [00:00<00:00, 64.0MB/s]

100%|██████████| 25.3M/25.3M [00:00<00:00, 56.4MB/s]

  0%|          | 0.00/3.54k [00:00<?, ?B/s]

100%|██████████| 3.54k/3.54k [00:00<00:00, 19.0MB/s]

/opt/hostedtoolcache/Python/3.12.13/x64/lib/python3.12/site-packages/cellpose/dynamics.py:760: UserWarning: Sparse invariant checks are implicitly disabled. Memory errors (e.g. SEGFAULT) will occur when operating on a sparse tensor which violates the invariants, but checks incur performance overhead. To silence this warning, explicitly opt in or out. See `torch.sparse.check_sparse_tensor_invariants.__doc__` for guidance.  (Triggered internally at /__w/pytorch/pytorch/aten/src/ATen/Context.cpp:816.)
  coo = torch.sparse_coo_tensor(pt, torch.ones(pt.shape[1], device=pt.device, dtype=torch.int),

  0%|          | 0.00/25.3M [00:00<?, ?B/s]

  1%|▏         | 336k/25.3M [00:00<00:07, 3.31MB/s]

  6%|▌         | 1.48M/25.3M [00:00<00:03, 8.04MB/s]

 26%|██▌       | 6.65M/25.3M [00:00<00:00, 28.4MB/s]

 69%|██████▉   | 17.6M/25.3M [00:00<00:00, 61.6MB/s]

100%|██████████| 25.3M/25.3M [00:00<00:00, 59.2MB/s]

  0%|          | 0.00/3.54k [00:00<?, ?B/s]

100%|██████████| 3.54k/3.54k [00:00<00:00, 14.4MB/s]

WARNING:ome_zarr.reader:no parent found for <ome_zarr.reader.Label object at 0x7f2bc908f770>: None

WARNING:ome_zarr.reader:no parent found for <ome_zarr.reader.Label object at 0x7f2bc891c6e0>: None

WARNING:ome_zarr.reader:no parent found for <ome_zarr.reader.Label object at 0x7f2b699bbce0>: None

WARNING:ome_zarr.reader:no parent found for <ome_zarr.reader.Label object at 0x7f2b6897e570>: None

WARNING:ome_zarr.reader:no parent found for <ome_zarr.reader.Label object at 0x7f2b6919f3b0>: None

WARNING:ome_zarr.reader:no parent found for <ome_zarr.reader.Label object at 0x7f2b688a80b0>: None

WARNING:ome_zarr.reader:no parent found for <ome_zarr.reader.Label object at 0x7f2b6870ecc0>: None

WARNING:ome_zarr.reader:no parent found for <ome_zarr.reader.Label object at 0x7f2bc931fc50>: None

WARNING:ome_zarr.reader:no parent found for <ome_zarr.reader.Label object at 0x7f2b687096d0>: None

WARNING:ome_zarr.reader:no parent found for <ome_zarr.reader.Label object at 0x7f2b68767d40>: None

WARNING:ome_zarr.reader:no parent found for <ome_zarr.reader.Label object at 0x7f2b6875fa10>: None

WARNING:ome_zarr.reader:no parent found for <ome_zarr.reader.Label object at 0x7f2b68dc1280>: None

WARNING:ome_zarr.reader:no parent found for <ome_zarr.reader.Label object at 0x7f2b69b95790>: None

WARNING:ome_zarr.reader:no parent found for <ome_zarr.reader.Label object at 0x7f2bc9059460>: None

WARNING:ome_zarr.reader:no parent found for <ome_zarr.reader.Label object at 0x7f2b6891a630>: None

WARNING:ome_zarr.reader:no parent found for <ome_zarr.reader.Label object at 0x7f2b692172c0>: None

WARNING:ome_zarr.reader:no parent found for <ome_zarr.reader.Label object at 0x7f2b69216990>: None

WARNING:ome_zarr.reader:no parent found for <ome_zarr.reader.Label object at 0x7f2b692452e0>: None

WARNING:ome_zarr.reader:no parent found for <ome_zarr.reader.Label object at 0x7f2b69273ce0>: None

WARNING:ome_zarr.reader:no parent found for <ome_zarr.reader.Label object at 0x7f2b68e57560>: None

WARNING:ome_zarr.reader:no parent found for <ome_zarr.reader.Label object at 0x7f2b691b6b10>: None

WARNING:ome_zarr.reader:no parent found for <ome_zarr.reader.Label object at 0x7f2b68c682f0>: None

WARNING:ome_zarr.reader:no parent found for <ome_zarr.reader.Label object at 0x7f2b68d34b00>: None

WARNING:ome_zarr.reader:no parent found for <ome_zarr.reader.Label object at 0x7f2b693e0800>: None

WARNING:ome_zarr.reader:no parent found for <ome_zarr.reader.Label object at 0x7f2b68d75fd0>: None

WARNING:ome_zarr.reader:no parent found for <ome_zarr.reader.Label object at 0x7f2b68dba7e0>: None

WARNING:ome_zarr.reader:no parent found for <ome_zarr.reader.Label object at 0x7f2b68c69910>: None

WARNING:ome_zarr.reader:no parent found for <ome_zarr.reader.Label object at 0x7f2b68e9d1f0>: None

WARNING:ome_zarr.reader:no parent found for <ome_zarr.reader.Label object at 0x7f2b691b54f0>: None

WARNING:ome_zarr.reader:no parent found for <ome_zarr.reader.Label object at 0x7f2b68e55e50>: None

WARNING:ome_zarr.reader:no parent found for <ome_zarr.reader.Label object at 0x7f2b68d43680>: None

WARNING:ome_zarr.reader:no parent found for <ome_zarr.reader.Label object at 0x7f2b691f9490>: None

WARNING:ome_zarr.reader:no parent found for <ome_zarr.reader.Label object at 0x7f2b68d03b90>: None

WARNING:ome_zarr.reader:no parent found for <ome_zarr.reader.Label object at 0x7f2b68919be0>: None

WARNING:ome_zarr.reader:no parent found for <ome_zarr.reader.Label object at 0x7f2b68d35fd0>: None

WARNING:ome_zarr.reader:no parent found for <ome_zarr.reader.Label object at 0x7f2bc97f8d10>: None

WARNING:ome_zarr.reader:no parent found for <ome_zarr.reader.Label object at 0x7f2b68da9850>: None

WARNING:ome_zarr.reader:no parent found for <ome_zarr.reader.Label object at 0x7f2b68c5aab0>: None

WARNING:ome_zarr.reader:no parent found for <ome_zarr.reader.Label object at 0x7f2b69215cd0>: None

WARNING:ome_zarr.reader:no parent found for <ome_zarr.reader.Label object at 0x7f2b68e9f440>: None

WARNING:ome_zarr.reader:no parent found for <ome_zarr.reader.Label object at 0x7f2b693e2db0>: None

Let’s look at the input images we processed.

project.plot_input_image()

Now we can look at the results generated by scPortrait. First, the segmentation masks.

project.plot_segmentation_masks()

And then extraction results consisting of individual single-cell images over all of the channels.

project.plot_single_cell_images()

Save and annotate results¶

Now we also want to save these results to the instance.

ln.Artifact.from_spatialdata(
    sdata=project.filehandler.get_sdata(),
    description="scportrait spatialdata object containing results of cells stained for autophagy markers",
    key=f"processed_data_imaging_use_case/{unique_project_id}/spatialdata.zarr",
).save()

# Define schemas for single-cell image dataset
schemas = {
    "obs": ln.Schema(
        name="single-cell image dataset schema obs",
        features=[
            ln.Feature(name="scportrait_cell_id", dtype="int", coerce_dtype=True).save()
        ],
    ).save(),
    "uns": ln.Schema(
        name="single-cell image dataset schema uns",
        features=[ln.Feature(name="single_cell_images", dtype=dict).save()],
    ).save(),
}

# Create composite schema
h5sc_schema = ln.Schema(
    name="single-cell image dataset",
    otype="AnnData",
    slots=schemas,
).save()

# Curate the AnnData object
curator = ln.curators.AnnDataCurator(project.h5sc, h5sc_schema)
curator.validate()

# Save artifact with annotations
artifact = curator.save_artifact(
    key=f"processed_data_imaging_use_case/{unique_project_id}/single_cell_data.h5ad"
)

# Add metadata and labels
annotation = shared_features.copy()
annotation["imaged structure"] = [
    ln.ULabel.connect("scportrait/examples").get(name=name)
    for name in ["LckLip-mNeon", "DNA", "mCherry-LC3B"]
]

artifact.features.add_values(annotation)
artifact.labels.add(ln.ULabel(name="scportrait single-cell images").save())

To process all files in our dataset efficiently, we’ll create a custom image processing function. We decorate this function with tracked() to track data lineage of the input and output artifacts.

The function will skip files that have already been processed and uploaded, improving processing time by avoiding redundant computations.

@ln.tracked()
def process_images(
    config_file_af: ln.Artifact,
    input_artifacts: Iterable[ln.Artifact],
    h5sc_schema: ln.Schema,
    output_directory: str,
) -> None:
    # Quick sanity check - all images should share metadata except channel/structure
    values_to_ignore = ["channel", "imaged structure"]
    first_features = input_artifacts.first().features.get_values()
    shared_features = {
        k: v for k, v in first_features.items() if k not in values_to_ignore
    }

    for artifact in input_artifacts:
        artifact_features = artifact.features.get_values()
        filtered_features = {
            k: v for k, v in artifact_features.items() if k not in values_to_ignore
        }
        assert shared_features == filtered_features

    # Create a unique project ID
    unique_project_id = f"{shared_features['cell_line_clone']}/{shared_features['stimulation']}/{shared_features['FOV']}".replace(
        " ", "_"
    )

    # Check if already processed
    base_key = f"processed_data_imaging_use_case/{unique_project_id}"
    try:
        ln.Artifact.connect("scportrait/examples").get(
            key=f"{base_key}/single_cell_data.h5ad"
        )
        ln.Artifact.connect("scportrait/examples").get(
            key=f"{base_key}/spatialdata.zarr"
        )
        print("Dataset already processed. Skipping.")
        return
    except ln.Artifact.DoesNotExist:
        pass

    # Get image paths in channel order
    input_image_paths = [
        input_artifacts.filter(ulabels__name=channel).one().cache()
        for channel in ["DAPI", "Alexa488", "mCherry"]
    ]

    # Setup and process project
    project_location = f"{output_directory}/{unique_project_id}/scportrait_project"
    Path(project_location).mkdir(parents=True, exist_ok=True)

    project = Project(
        project_location=project_location,
        config_path=config_file_af.cache(),
        segmentation_f=CytosolSegmentationCellpose,
        extraction_f=HDF5CellExtraction,
        overwrite=True,
    )

    project.load_input_from_tif_files(
        input_image_paths, overwrite=True, channel_names=["DAPI", "Alexa488", "mCherry"]
    )
    project.segment()
    project.extract()

    # Save single-cell images
    curator = ln.curators.AnnDataCurator(project.h5sc, h5sc_schema)
    curator.validate()
    artifact = curator.save_artifact(key=f"{base_key}/single_cell_data.h5ad")

    annotation = shared_features.copy()
    annotation["imaged structure"] = [
        ln.ULabel.connect("scportrait/examples").get(name=name)
        for name in ["LckLip-mNeon", "DNA", "mCherry-LC3B"]
    ]

    artifact.features.add_values(annotation)
    artifact.labels.add(ln.ULabel.get(name="scportrait single-cell images"))

    # Save SpatialData object
    ln.Artifact.from_spatialdata(
        sdata=project.filehandler.get_sdata(),
        description="scportrait spatialdata object containing results of cells stained for autophagy markers",
        key=f"{base_key}/spatialdata.zarr",
    ).save()

Now we are ready to process all of our input images and upload the generated single-cell image datasets back to our instance.

for condition in conditions:
    for cellline in cell_line_clones:
        for FOV in FOVs:
            images = (
                input_images.filter(ulabels=condition)
                .filter(ulabels=cellline)
                .filter(ulabels=FOV)
                .distinct()
            )

            if images:
                process_images(
                    config_file_af,
                    input_artifacts=images,
                    h5sc_schema=h5sc_schema,
                    output_directory=output_directory,
                )

Show code cell output Hide code cell output

→ ignoring transform with same filename in different folder:
    BS6hWDeKg5uw0000 → sc-imaging2.ipynb

→ created Transform('wHT5luVhbZuY0000', key='sc-imaging2.ipynb'), started new Run('6FOn7SshUcyA6wuY', entrypoint='process_images') at 2026-07-12 19:21:17 UTC
→ params: config_file_af='Artifact[voi8szTkmKPiahUA0000]', input_artifacts=['Artifact[Md4OouMExlWS2YfZ0000]', 'Artifact[CiQYTBNZrj0CPejK0000]', 'Artifact[YGiNq6DPfIEjtt9j0000]'], h5sc_schema='Schema[riBnQ2kagmv0eldX]', output_directory='processed_data'

Dataset already processed. Skipping.

→ loaded Transform('wHT5luVhbZuY0000', key='sc-imaging2.ipynb'), started new Run('A4nUlEd2xcY6VOs0', entrypoint='process_images') at 2026-07-12 19:21:18 UTC
→ params: config_file_af='Artifact[voi8szTkmKPiahUA0000]', input_artifacts=['Artifact[KKbVRkOjQ1jdA2fx0000]', 'Artifact[W6tzE7JNiM80Ruho0000]', 'Artifact[uuh41FAHEz0ASL2N0000]'], h5sc_schema='Schema[riBnQ2kagmv0eldX]', output_directory='processed_data'

Dataset already processed. Skipping.

→ loaded Transform('wHT5luVhbZuY0000', key='sc-imaging2.ipynb'), started new Run('KbGSWKjjdfAcJBYg', entrypoint='process_images') at 2026-07-12 19:21:19 UTC
→ params: config_file_af='Artifact[voi8szTkmKPiahUA0000]', input_artifacts=['Artifact[yiIMSAddDWgLgki70000]', 'Artifact[DEzw4QQAsjVZ010b0000]', 'Artifact[hbVyCGFARHU91Kax0000]'], h5sc_schema='Schema[riBnQ2kagmv0eldX]', output_directory='processed_data'

Dataset already processed. Skipping.

→ loaded Transform('wHT5luVhbZuY0000', key='sc-imaging2.ipynb'), started new Run('lyz00EZtxRllYsck', entrypoint='process_images') at 2026-07-12 19:21:19 UTC
→ params: config_file_af='Artifact[voi8szTkmKPiahUA0000]', input_artifacts=['Artifact[2ie2Kjzn1O7UYhuq0000]', 'Artifact[fOQSb7JCK67aeN6a0000]', 'Artifact[qHQpdWcFu7FzF6l50000]'], h5sc_schema='Schema[riBnQ2kagmv0eldX]', output_directory='processed_data'

Dataset already processed. Skipping.

→ loaded Transform('wHT5luVhbZuY0000', key='sc-imaging2.ipynb'), started new Run('5Hg4tTOuZ38333t9', entrypoint='process_images') at 2026-07-12 19:21:20 UTC
→ params: config_file_af='Artifact[voi8szTkmKPiahUA0000]', input_artifacts=['Artifact[jVytS8AyAHmHkYR30000]', 'Artifact[cw4F6bUB9zuMthCY0000]', 'Artifact[7TZGXvbA0JLL68hR0000]'], h5sc_schema='Schema[riBnQ2kagmv0eldX]', output_directory='processed_data'

Dataset already processed. Skipping.

→ loaded Transform('wHT5luVhbZuY0000', key='sc-imaging2.ipynb'), started new Run('kZJ80L7ntPMLqNtP', entrypoint='process_images') at 2026-07-12 19:21:21 UTC
→ params: config_file_af='Artifact[voi8szTkmKPiahUA0000]', input_artifacts=['Artifact[vCVbKkzz4CnJPPKF0000]', 'Artifact[5kMhlcDNek4RMeQF0000]', 'Artifact[9BmbViqMmlVhpfS00000]'], h5sc_schema='Schema[riBnQ2kagmv0eldX]', output_directory='processed_data'

Dataset already processed. Skipping.

→ loaded Transform('wHT5luVhbZuY0000', key='sc-imaging2.ipynb'), started new Run('atSzDNYsKRMgIdul', entrypoint='process_images') at 2026-07-12 19:21:21 UTC
→ params: config_file_af='Artifact[voi8szTkmKPiahUA0000]', input_artifacts=['Artifact[OS0wBE7bviIlW7qj0000]', 'Artifact[ixOpuSTsyrPXdYuA0000]', 'Artifact[6uMjKAk1aYlAV7Cf0000]'], h5sc_schema='Schema[riBnQ2kagmv0eldX]', output_directory='processed_data'

Dataset already processed. Skipping.

→ loaded Transform('wHT5luVhbZuY0000', key='sc-imaging2.ipynb'), started new Run('zFEFB7x3Mw0PAGga', entrypoint='process_images') at 2026-07-12 19:21:22 UTC
→ params: config_file_af='Artifact[voi8szTkmKPiahUA0000]', input_artifacts=['Artifact[9ZVngbl0JUS0XdZ70000]', 'Artifact[IzP3IAwIhmM7OORD0000]', 'Artifact[RRVS8qVx3VSw02Xu0000]'], h5sc_schema='Schema[riBnQ2kagmv0eldX]', output_directory='processed_data'

Dataset already processed. Skipping.

→ loaded Transform('wHT5luVhbZuY0000', key='sc-imaging2.ipynb'), started new Run('P5zcHgtinCbVSKWj', entrypoint='process_images') at 2026-07-12 19:21:23 UTC
→ params: config_file_af='Artifact[voi8szTkmKPiahUA0000]', input_artifacts=['Artifact[Gtwi9Pcyx8maQEWB0000]', 'Artifact[sHHpiiFYWsIXMZNV0000]', 'Artifact[hNMkrIHce1XrLZHY0000]'], h5sc_schema='Schema[riBnQ2kagmv0eldX]', output_directory='processed_data'

Dataset already processed. Skipping.

→ loaded Transform('wHT5luVhbZuY0000', key='sc-imaging2.ipynb'), started new Run('vfB8PyC8Ly0vIX9l', entrypoint='process_images') at 2026-07-12 19:21:24 UTC
→ params: config_file_af='Artifact[voi8szTkmKPiahUA0000]', input_artifacts=['Artifact[nSZhAypqiNZ2Ylbe0000]', 'Artifact[jzqxtoduIJ3hCbB40000]', 'Artifact[M06liaIzh2OVEuJ40000]'], h5sc_schema='Schema[riBnQ2kagmv0eldX]', output_directory='processed_data'

Dataset already processed. Skipping.

→ loaded Transform('wHT5luVhbZuY0000', key='sc-imaging2.ipynb'), started new Run('a4gcdjeS4XH9hpFZ', entrypoint='process_images') at 2026-07-12 19:21:24 UTC
→ params: config_file_af='Artifact[voi8szTkmKPiahUA0000]', input_artifacts=['Artifact[mXWwV1x42Jz9RoSO0000]', 'Artifact[gj0HHnoVpEqbaUJb0000]', 'Artifact[1XnEyqVt6UGXCTmV0000]'], h5sc_schema='Schema[riBnQ2kagmv0eldX]', output_directory='processed_data'

Dataset already processed. Skipping.

→ loaded Transform('wHT5luVhbZuY0000', key='sc-imaging2.ipynb'), started new Run('eQOP0t4lBdY9O8BU', entrypoint='process_images') at 2026-07-12 19:21:25 UTC
→ params: config_file_af='Artifact[voi8szTkmKPiahUA0000]', input_artifacts=['Artifact[Ov8FnKzHMNY0XVJa0000]', 'Artifact[Lwk8shsYe0V5bMgd0000]', 'Artifact[YuyVn060M4FxATPz0000]'], h5sc_schema='Schema[riBnQ2kagmv0eldX]', output_directory='processed_data'

Dataset already processed. Skipping.

→ loaded Transform('wHT5luVhbZuY0000', key='sc-imaging2.ipynb'), started new Run('aPb8BuNssXbICkDU', entrypoint='process_images') at 2026-07-12 19:21:26 UTC
→ params: config_file_af='Artifact[voi8szTkmKPiahUA0000]', input_artifacts=['Artifact[ThuJnRAhqkp54kyU0000]', 'Artifact[PquYNyshQTDd24Vw0000]', 'Artifact[8SFUmW0RhBNySxBO0000]'], h5sc_schema='Schema[riBnQ2kagmv0eldX]', output_directory='processed_data'

Dataset already processed. Skipping.

→ loaded Transform('wHT5luVhbZuY0000', key='sc-imaging2.ipynb'), started new Run('ZRAJ6d7hFJZagtiM', entrypoint='process_images') at 2026-07-12 19:21:27 UTC
→ params: config_file_af='Artifact[voi8szTkmKPiahUA0000]', input_artifacts=['Artifact[h4EKWveW36LIzXez0000]', 'Artifact[fdem35nw5ztUnEIM0000]', 'Artifact[VkmKLUCaMsYFCuGE0000]'], h5sc_schema='Schema[riBnQ2kagmv0eldX]', output_directory='processed_data'

Dataset already processed. Skipping.

→ loaded Transform('wHT5luVhbZuY0000', key='sc-imaging2.ipynb'), started new Run('IFB2muSptOeVw6gl', entrypoint='process_images') at 2026-07-12 19:21:27 UTC
→ params: config_file_af='Artifact[voi8szTkmKPiahUA0000]', input_artifacts=['Artifact[QDPX1ljp0eCMz80o0000]', 'Artifact[Cvamog4G3a2XYGM80000]', 'Artifact[6uUjyphUD4D1Hixc0000]'], h5sc_schema='Schema[riBnQ2kagmv0eldX]', output_directory='processed_data'

Dataset already processed. Skipping.

→ loaded Transform('wHT5luVhbZuY0000', key='sc-imaging2.ipynb'), started new Run('wiCxKSg034Duj9uh', entrypoint='process_images') at 2026-07-12 19:21:28 UTC
→ params: config_file_af='Artifact[voi8szTkmKPiahUA0000]', input_artifacts=['Artifact[Oww4y0yYuR8pxV9q0000]', 'Artifact[AhBvnNKg5yJcG6LU0000]', 'Artifact[AVRTVX9gEu4LrTAP0000]'], h5sc_schema='Schema[riBnQ2kagmv0eldX]', output_directory='processed_data'

Dataset already processed. Skipping.

example_artifact = ln.Artifact.filter(
    ulabels=ln.ULabel.get(name="scportrait single-cell images")
).first()

example_artifact.view_lineage()

ln.finish()