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Synthetic lumen rounding directs neural progenitor division mode

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  1. [1] § Methods › Image analysis › Organoid 2D analysis ↔ Thickness-masks-measurements/Thickness-measurements-updated.py.R, lines 46–108 · score 0.57 · MajorAxis, largest, thickness, Fiji, circularity, masks

Paper

Loaded from Europe PMC by your browser, not stored by OSCR: doi.org · Europe PMC

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The authors' code

R · 152 lines · 4.5 KB · no license · 1 match

  1. #!/usr/bin/env python3
  2. # -*- coding: utf-8 -*-
  3. """
  4. Created on Fri Mar 20 16:00:42 2026
  5. @author: marchenk
  6. """
  7. import math
  8. import numpy as np
  9. import tifffile as tif
  10. from skimage.measure import label, regionprops
  11. from skimage.morphology import remove_small_objects
  12. from scipy.ndimage import binary_fill_holes
  13. import os
  14. import pandas as pd
  15. from skimage.measure import regionprops_table
  16. def analyze_thickness_tiff(
  17. tiff_path,
  18. min_object_size=50,
  19. connectivity=2
  20. ):
  21. img = tif.imread(tiff_path).astype(float)
  22. mask = img > 0
  23. mask = remove_small_objects(mask, min_size=min_object_size)
  24. labeled = label(mask, connectivity=connectivity)
  25. measurements = []
  26. for region in regionprops(labeled, intensity_image=img):
  27. # -----------------------------
  28. # Thickness statistics
  29. # -----------------------------
  30. thickness = region.intensity_image[region.intensity_image > 0]
  31. if thickness.size == 0:
  32. continue
  33. mean_thickness = thickness.mean()
  34. std_thickness = thickness.std()
  35. cv_thickness = std_thickness / mean_thickness if mean_thickness > 0 else np.nan
  36. # -----------------------------
  37. # Area, perimeter & Roundness (FIJI MATCHING)
  38. # -----------------------------
  39. # 1. Area: The actual pixels of the ring (as you defined in Fiji)
  40. area = region.area
  41. # 2. Perimeter: Use standard perimeter (better Fiji match than Crofton)
  42. perimeter = region.perimeter_crofton
  43. # 3. Major Axis: To match Fiji, we find the axis of the FILLED shape
  44. # region.image is the ring; region.filled_image is the ring + lumen
  45. filled_label = label(region.filled_image.astype(int))
  46. filled_props = regionprops(filled_label)
  47. if filled_props:
  48. # We take the major axis of the solid version of this object
  49. fiji_major_axis = filled_props[0].major_axis_length
  50. else:
  51. fiji_major_axis = region.major_axis_length
  52. # Fiji Roundness: 4 * Area / (pi * (MajorAxis of filled shape)^2)
  53. circularity = (4 * area) / (np.pi * (fiji_major_axis**2)) if fiji_major_axis > 0 else np.nan
  54. # -----------------------------
  55. # Lumen (hole) perimeter
  56. # -----------------------------
  57. object_mask = region.image # binary mask in bounding box
  58. filled = binary_fill_holes(object_mask)
  59. holes = filled & (~object_mask)
  60. lumen_perimeter = np.nan
  61. if holes.any():
  62. hole_labels = label(holes, connectivity=connectivity)
  63. hole_regions = regionprops(hole_labels)
  64. if hole_regions:
  65. # Select largest hole = lumen
  66. lumen = max(hole_regions, key=lambda r: r.area)
  67. # Using standard perimeter for lumen too for consistency
  68. lumen_perimeter = lumen.perimeter
  69. measurements.append({
  70. "mean_thickness": mean_thickness,
  71. "std_thickness": std_thickness,
  72. "cv_thickness": cv_thickness,
  73. "area_pixels": area,
  74. "perimeter_pixels": perimeter,
  75. "circularity": circularity,
  76. "lumen_perimeter": lumen_perimeter
  77. })
  78. return measurements
  79. def process_folder(
  80. input_folder,
  81. output_folder,
  82. output_csv_name="thickness_measurements.csv",
  83. min_object_size=50,
  84. connectivity=2
  85. ):
  86. all_results = []
  87. # Filter for tiff files
  88. files = [f for f in os.listdir(input_folder) if f.lower().endswith((".tif", ".tiff"))]
  89. if not files:
  90. print(f"No TIFF files found in {input_folder}")
  91. return pd.DataFrame()
  92. for file_name in files:
  93. file_path = os.path.join(input_folder, file_name)
  94. object_measurements = analyze_thickness_tiff(
  95. file_path,
  96. min_object_size=min_object_size,
  97. connectivity=connectivity
  98. )
  99. for idx, obj in enumerate(object_measurements, start=1):
  100. all_results.append({
  101. "file_name": file_name,
  102. "object_id": idx,
  103. **obj
  104. })
  105. os.makedirs(output_folder, exist_ok=True)
  106. df = pd.DataFrame(all_results)
  107. output_path = os.path.join(output_folder, output_csv_name)
  108. df.to_csv(output_path, index=False)
  109. return df
  110. # --- Execution ---
  111. input_folder = r"" # Set your input path
  112. output_folder = r"" # Set your output path
  113. df = process_folder(
  114. input_folder=input_folder,
  115. output_folder=output_folder,
  116. output_csv_name="thickness_results.csv",
  117. )
  118. if not df.empty:
  119. print(df.head())

Thickness-measurements-updated.py.R at commit 20c58ed, no license · at the source

Overview

  1. Cluster of Excellence Physics of Life, TU Dresden, Dresden, Germany
  2. European Molecular Biology Laboratory, EMBL Barcelona, C/ Dr. Aiguader, 88, PRBB Building, 08003, Barcelona, Spain
  3. Department of Computational and Systems Biology, School of Medicine, University of Pittsburgh, Pittsburgh, PA, USA
  4. Max Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany
Dates: published online 1 April 2026
Type: Preprint
License: CC BY
Identifiers: DOI 10.64898/2026.03.30.715222 · OpenAlex W7147174344
Open access: green, a free copy (OpenAlex)
Status: code verified
Categories: developmental (subfield)
Methods: Statistics, Evoked potentials
Topic: Planarian Biology and Electrostimulation (Molecular Biology, Biochemistry, Genetics and Molecular Biology), according to OpenAlex
Citations: cited by 1 paper (Europe PMC); 49 references in the paper

Abstract

Although function often follows form, the causal role of tissue geometry is difficult to disentangle in complex embryonic development. Brain organoids generated using diverse protocols and species display striking morphological variability, particularly in lumen shape; however, whether and how lumen geometry influences neural development remains unclear. Here, we manipulate lumen sphericity in human cerebral organoids by acutely inducing apical constriction and reveal its impact on the division orientation of apical progenitors. Rapid protein stabilization or optogenetic reconstitution of the apical constriction regulator Shroom3 induces pronounced lumen rounding accompanied by a reduction in apical surface area. In organoids with rounded lumens, apical progenitor divisions shift toward horizontal cleavage planes compared with control organoids, consistent with geometric constraints from the reduced apical surface. Accordingly, rounded-lumen organoids exhibit increased cell delamination and an earlier emergence of basal progenitors in the abventricular region. These findings identify lumen geometry as an instructive regulator of progenitor division mode and lineage progression during early brain development.

Reproduced under the paper's license (CC BY), from the paper cited above.

Repository

Its files are read in the Code ↔ Paper reader above, with 1 match between paragraphs and lines of code.

mebisuya/BrainOrganoidShape

License: none: the authors keep all their rights
State: the link answers, verified on 28 September 2026
Evidence: files inventoried
Commit: 20c58ed341040a7d110ce214901f9cbf4de4f928, 22 March 2026
Languages: R (4), Jupyter (3)
Size: 16 files, 7 scripts
Software Heritage: not archived
Found in: “Data and materials availability”
Holds: environment (Angle-fusion-tif-main/env.yml), 3 notebooks
Not found: README, license file, CITATION.cff, tests, continuous integration, documentation
Tools: NumPy (3 files), scikit-image (3 files), Matplotlib (2 files), SciPy (2 files), OpenCV (1 file), pandas (1 file), PyTorch (1 file), scikit-learn (1 file), seaborn (1 file), tifffile (1 file)
Availability: 1 check, the latest on 28 September 2026: the link answers
  • 28 September 2026: the link answers
7 files

The paper's code and data availability statement is in the Data section.

Tracing map

Proposed by the machine: these links were found in the paper and verified at the source, without human review. The map will receive a Zenodo DOI once one of the paper's authors has validated it with their ORCID.

What the map holds:

  • 1 repository of the authors' code, each at its verified commit, with its license and how the link was found in the paper;
  • 7 scripts, each with its path and the digest of its content;
  • 1 match between paragraphs of the paper and lines of the code (method lexical-v1);
  • neither the text of the paper nor the code itself.

Its JSON (tracing-map.json) is deposited on Zenodo with its DOI once the map is validated.

Data

No dataset and no data link were found in the paper.

Data and materials availability

The custom scripts used are available from Github [https://github.com/mebisuya/BrainOrganoidShape].

Reproduced under the paper's license (CC BY), from the paper cited above.

Versions

The history of this record: each version stored by the harvester or made by a correction of its authors or of the maintainers of its code, and what changed in its facts. The texts of the paper (its abstract, its availability statements) are not part of it; versions that changed only those are not listed.

Version 2, 28 September 2026

  • Authors: added Marina Marchenko (0000-0002-0473-9430); Guillermo Martínez Ara (0000-0002-7480-5595); removed Marina Marchenko; Guillermo Martínez Ara

Version 1, 28 September 2026: the first record

Recorded: type, journal, dates, 5 authors, 47 references.

Cite

This paper

Marchenko, M., Martínez Ara, G., Pulikkal, J., Ishihara, K., & Ebisuya, M. (2026). Synthetic lumen rounding directs neural progenitor division mode. bioRxiv (preprint). https://doi.org/10.64898/2026.03.30.715222

BibTeX

@article{marchenko2026synthetic,
author = {Marchenko, Marina and Martínez Ara, Guillermo and Pulikkal, Juslina and Ishihara, Keisuke and Ebisuya, Miki},
title = {{Synthetic lumen rounding directs neural progenitor division mode}},
journal = {bioRxiv (preprint)},
year = {2026},
month = apr,
publisher = {bioRxiv},
issn = {2692-8205},
doi = {10.64898/2026.03.30.715222},
url = {https://doi.org/10.64898/2026.03.30.715222}
}

RIS

TY - JOUR
AU - Marchenko, Marina
AU - Martínez Ara, Guillermo
AU - Pulikkal, Juslina
AU - Ishihara, Keisuke
AU - Ebisuya, Miki
TI - Synthetic lumen rounding directs neural progenitor division mode
T2 - bioRxiv (preprint)
J2 - bioRxiv
PY - 2026
DA - 2026/04/01
SN - 2692-8205
PB - bioRxiv
DO - 10.64898/2026.03.30.715222
UR - https://doi.org/10.64898/2026.03.30.715222
ER -

CSL-JSON

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"id": "10.64898/2026.03.30.715222",
"type": "article",
"title": "Synthetic lumen rounding directs neural progenitor division mode",
"container-title": "bioRxiv (preprint)",
"author": [
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"family": "Marchenko",
"given": "Marina"
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"family": "Martínez Ara",
"given": "Guillermo"
},
{
"family": "Pulikkal",
"given": "Juslina"
},
{
"family": "Ishihara",
"given": "Keisuke"
},
{
"family": "Ebisuya",
"given": "Miki"
}
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"container-title-short": "bioRxiv",
"DOI": "10.64898/2026.03.30.715222",
"ISSN": "2692-8205",
"publisher": "bioRxiv",
"URL": "https://doi.org/10.64898/2026.03.30.715222",
"issued": {
"date-parts": [
[
2026,
4,
1
]
]
}
}

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