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Annotate/Classify example data: 2341 crops, 88 labels, portable paths

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  1. .gitattributes +1 -0
  2. README.md +72 -0
  3. data/multiple_nucleus/multiple_pathogens/plate1_E01/cell_png/.spacr_crop_format.json +7 -0
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  43. data/multiple_nucleus/multiple_pathogens/plate1_L01/cell_png/.spacr_crop_format.json +7 -0
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.gitattributes CHANGED
@@ -58,3 +58,4 @@ saved_model/**/* filter=lfs diff=lfs merge=lfs -text
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  # Video files - compressed
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  *.mp4 filter=lfs diff=lfs merge=lfs -text
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  *.webm filter=lfs diff=lfs merge=lfs -text
 
 
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  # Video files - compressed
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  *.mp4 filter=lfs diff=lfs merge=lfs -text
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  *.webm filter=lfs diff=lfs merge=lfs -text
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+ measurements.db filter=lfs diff=lfs merge=lfs -text
README.md ADDED
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+ ---
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+ license: mit
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+ task_categories:
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+ - image-classification
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+ tags:
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+ - spacr
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+ - microscopy
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+ - annotation
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+ - toxoplasma
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+ pretty_name: spaCR Annotate and Classify example data
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+ ---
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+
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+ # spaCR — Annotate and Classify example data
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+
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+ Example input for the **Annotate** and **Classify** modules of
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+ [spaCR](https://github.com/EinarOlafsson/spacr). It is the output of a Measure
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+ run, so both modules can be exercised without segmenting or measuring anything
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+ first.
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+
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+ ## What is here
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+
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+ | Path | What it is |
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+ |---|---|
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+ | `data/` | 2,341 single-cell PNG crops, foldered by phenotype |
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+ | `measurements.db` | The measurements, plus `png_list` and the annotation tables |
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+ | `measurements/active_learning/` | The model card from the first annotation round |
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+ | `settings/annotate_settings.csv` | Settings for the Annotate module |
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+ | `settings/classify_settings.csv` | Settings for the Classify module |
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+
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+ ## It carries real annotations
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+
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+ `png_list.annotate` holds **88 labels** — 50 of class 1 and 38 of class 2 —
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+ against 2,253 unlabelled crops, with 101 rows of per-round history in
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+ `annotation_rounds`. That is what makes this usable as a *classify* set: a
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+ training example needs labels, and unlabelled crops alone would only exercise
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+ the viewer.
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+
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+ The first active-learning round is recorded too: 88 labels, 25 held out by
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+ well, `holdout_accuracy` 1.0 on a `StratifiedGroupKFold` split where no well
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+ appears on both sides. Treat that number as a demonstration of the workflow,
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+ not as a result — 88 labels over four wells is a very small set.
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+
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+ ## Paths are RELATIVE, deliberately
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+
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+ Every path in `measurements.db` and in both settings files is relative to the
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+ dataset root:
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+
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+ ```
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+ data/single_nucleus/uninfected/plate1_E01/cell_png/plate1_E01_19_1_12.png
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+ ```
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+
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+ A measurements database normally stores absolute paths, which name the machine
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+ that made it and resolve nowhere else. spaCR's downloader rewrites these to
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+ absolute on arrival, so the database works wherever it is unpacked. If you
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+ unpack it by hand, do the same, or point spaCR at the folder and let it.
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+
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+ `<dataset>` in the settings files is a placeholder for the unpack location and
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+ is substituted the same way.
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+
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+ ## Plate layout
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+
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+ Four wells (E01, E02, L01, L02) from the plate published as
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+ [`einarolafsson/spacr-example-measure`](https://huggingface.co/datasets/einarolafsson/spacr-example-measure),
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+ which holds the merged arrays these crops were cut from.
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+
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+ ## Provenance
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+
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+ Produced by spaCR's Mask module and then its Measure module, from spaCR's own
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+ example images, with `cpsam` for cells and nuclei and a Toxoplasma-specific
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+ CPSAM checkpoint for pathogens. One field of fifty-two (`plate1_E02_20_1`)
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+ failed to measure — a nucleus label spanning two cells — so the crops come from
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+ 51 fields. Absolute paths have been rewritten to relative throughout.
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+ {
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+ "channel_order": "declared_rgb",
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+ "narrowing": "high-byte",
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+ "note": "The red, green and blue channels hold the source channels named by settings['png_channel_mapping']. No list-position convention is involved, so there is nothing here to read backwards.",
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+ "spacr_crop_format": 3,
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+ "updated_utc": "2026-09-01T18:48:32Z"
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+ }
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