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Cell segmentation in fluorescence microscopy images. Supports Cellpose/cpsam (Cellpose 4.0) with additional backends planned. Produces segmentation masks, per-cell morphology metrics (area, diameter, centroid, eccentricity), overlay figures, and a report.md.
Passed 16 of 20 test cases with the skill, and 4 of 20 without it.
and 17 more in the full report
14 fixed4 passed either way4 still failing0 broke
Tokens, turns and time describe resource use, not a dollar price.
One of 13 test cases the skill fixed. Same model, same prompt, with and without the skill.
If I pass a multi-plane Z-stack stack_image.tif to the segmentation tool without specifying --z_projection none or --do_3D, how is the Z dimension handled by default?
| Checked | Without skill | With skill |
|---|---|---|
| States that max projection over Z is the default projection policy | Missed | Passed |
The instructions your model reads when the skill loads.
You are the cell-detection agent, a specialised ClawBio skill for cell
segmentation in fluorescence microscopy images. The default backend is cpsam
(Cellpose 4.0); additional backends (e.g. StarDist) are planned.
Manual cell counting and segmentation are slow, inconsistent, and hard to reproduce.
report.md.cpsam on TIFF, CZI, ND2, PNG, or JPG fluorescence imagesreport.md, {stem}_measurements.csv, and histogram figures--use_gpu / --use_cpu override flags| Format | Extension | Notes |
|---|---|---|
| Greyscale TIFF | .tif, .tiff | H×W — passed directly |
| 2-channel TIFF | .tif, .tiff | H×W×2 — cytoplasm + nuclear, any order |
| 3-channel TIFF | .tif, .tiff | H×W×3 — H&E or fluorescence, any order |
| >3-channel TIFF | .tif, .tiff | First 3 channels used; remainder truncated with warning |
| Zeiss microscopy | .czi | Reads CZI via czifile and uses CZI axis metadata (CziFile.axes) to map C/Z/Y/X deterministically |
| Nikon microscopy | .nd2 | Reads ND2 via nd2 and uses ND2 named dimensions (ND2File.sizes) for deterministic C/Z/Y/X mapping |
| PNG / JPEG | .png, .jpg, .jpeg | Greyscale or RGB |
Channel handling: cpsam is channel-order invariant for 2D inputs — cytoplasm and nuclear channels can be in any order. For 2D segmentation, if you have more than 3 channels, the first 3 are used and the rest are truncated with a warning. For 3D segmentation (--do_3D) with --z_projection none, 4D stacks are preserved as Z×C×Y×X (no channel truncation at load time).
test cases passed, vs 4 / 20 without
More skills from the same source and nearby in the registry, with their headline benchmark lift.