Quality control pipeline for MACSima / MACSiQView cell segmentation
Python package for evaluating and comparing cell segmentation results from the MACSima cyclic immunofluorescence platform, using manual ROI references from Fiji/ImageJ.
pip install macsima-qcOr from source (development mode):
git clone https://github.com/mathisbouvet/macsima-qc
cd macsima-qc
pip install -e .MACSiQView segmentation (.csv)
│
run_qc_pipeline() ← Isolation Forest + Mann-Whitney
│
┌───────┴────────────────────────┐
│ segmentation_test_annotated.csv │ ← OK / KO labels per cell
│ macsiq_param_suggestions.csv │ ← MACSiQView adjustment suggestions
└─────────────────────────────────┘
── Optional ──────────────────────────────────────────────
Fiji ROIs (.zip) ──► generate_masks() ──► run_comparison() ← KS distances + KDE
No reference file needed. Just point to your MACSiQView segmentation CSV:
from macsima_qc import run_qc_pipeline
df_annotated, df_suggestions = run_qc_pipeline(
test_path="Segmentation_test.csv",
contamination=0.10,
output_dir="figures/",
)If you want to use your own manually validated segmentation as reference:
from macsima_qc import run_qc_pipeline
df_annotated, df_suggestions = run_qc_pipeline(
test_path="Segmentation_test.csv",
ref_path="my_reference.csv",
contamination=0.10,
)After segmentation in MACSiQView, navigate to the Feature Table tab and select the following 14 morphological parameters for export. Only morphological descriptors are used, fluorescence intensities are excluded.
| Parameter | Description |
|---|---|
Cell Bbox X Size |
Bounding box width |
Cell Bbox Y Size |
Bounding box height |
Cell Shape Circle Like |
Circularity index |
Cell Shape Ellipse Like |
Ellipse similarity |
Cell Shape Elongation |
Elongation ratio |
Cell Shape Square Like |
Square similarity |
Cell Shape Triangle Like |
Triangle similarity |
Cell Size |
Cell area |
Nucleus Size |
Nucleus area |
Nucleus Roundness |
Nucleus roundness |
Nucleus Convexity |
Nucleus convexity |
Cell Convexity |
Cell convexity |
Quality Cell In-Focus |
Focus quality score |
Quality Nuclear Segmentation |
Nuclear segmentation quality |
These 14 features are mandatory. The pipeline will raise an error if any are missing from the exported CSV.
- In MACSiQView, open the Feature Table panel
- Select the 14 parameters listed above
- Export as
.csv - This exported file is your
test_pathinput forrun_qc_pipeline()
The package ships with a built-in reference segmentation derived from a manually validated MACSima acquisition (DAPI channel, human embryonic tissue). It contains 4,641 cells described by the same 14 morphological features listed above, exported using the exact same MACSiQView protocol.
If your tissue type differs significantly from human embryonic tissue (e.g. non-embryonic tissue, very different cell density or morphology), consider providing your own reference via
ref_path.
Before fixing the contamination parameter, the model sensitivity is analyzed across a range of values (0.01 → 0.20). The Isolation Forest is then trained exclusively on the reference data. Each test cell receives a label (Segmentation_OK: 1 or -1) and a continuous anomaly score.
The Mann-Whitney U test then compares OK vs KO distributions for each feature. When a statistically significant difference is found (p < 0.01), the direction of deviation is translated into an operational MACSiQView adjustment suggestion, exported to macsiq_param_suggestions.csv.
| File | Description |
|---|---|
mask_1–4.tif |
ROI masks for MACSiQView import |
figures/ks_average_distances.png |
KS distance barplot per segmentation |
figures/kde_comparative_distributions.png |
KDE distribution comparison |
figures/contamination_sensitivity.png |
Isolation Forest sensitivity curve |
figures/anomaly_scores_distribution.png |
Anomaly score histogram |
segmentation_test_annotated.csv |
Cells annotated OK/KO + anomaly score |
macsiq_param_suggestions.csv |
MACSiQView parameter adjustment suggestions |
Anomaly score distribution from the Isolation Forest — cells below the decision threshold are flagged as Segmentation_KO.
For the full step-by-step protocol, see the 01_segmentation_qc.
A reference DAPI image is extracted from the MACSima system and exported in .tif format for processing in Fiji. Regions of interest (ROI) are manually drawn to serve as the basis for segmentation masks.
- DAPI Image : exported in
tiffformat via MACSima - RoiSet : created and exported from Fiji in
zipformat
Once the ROIs are defined, four types of masks are generated and imported into MACSiQView as segmentation inputs:
| File | Description |
|---|---|
mask_1.tif |
ROIs with random colors, black background |
mask_2.tif |
ROIs with cyclic RGB colors (R/G/B), black background |
mask_3.tif |
ROIs in cumulative grayscale |
mask_4.tif |
ROIs in cumulative grayscale + black contours |
from macsima_qc import run_comparison
distances = run_comparison(
manual_path = "Segmentation_manuelle.csv",
auto_paths = [
"Mask_3_Single_Cell.csv",
"Mask_3_Tissue.csv",
"Mask_4_Import_mask.csv",
"Mask_4_Single_Cell.csv",
"Mask_4_Tissue.csv",
],
auto_names = [
"Mask 3 - Single Cell",
"Mask 3 - Tissue",
"Mask 4 - Import Mask",
"Mask 4 - Single Cell",
"Mask 4 - Tissue",
],
output_dir = "figures/",
)This produces a barplot of average KS distances and KDE distribution curves for the main morphological parameters, identifying the automatic segmentation closest to the manual reference.
Lower KS distance = closer match to the manual reference. Here, Mask 4 – Single Cell performs best across most morphological parameters.
- Python ≥ 3.9
- numpy, opencv-python, matplotlib, scikit-image, read-roi
- pandas, scikit-learn, scipy, seaborn
If you use this package in a publication, please cite:
Bouvet M. (2026)
MIT




