OSCR

SPOmiAlign: a modality-agnostic computational framework for multimodal spatial omics alignment enabled by a feature matching foundation model.

Code ↔ Paper

8 matches between paragraphs of the paper and lines of its authors' code, computed by the harvester (lexical-v1). Click a colored paragraph or line to see its counterpart.

The 8 matches
  1. [1] § Methods › Data preprocessing in SPOmiAlign ↔ SHARP-Track/Convert_CCF_Coords_to_FP_Regions.m, lines 11–47 · score 0.77 · coordinate transformation, Allen CCF, annotation volume, mouse brain, Brain Atlas, spaced
  2. [2] § Methods › Data preprocessing in SPOmiAlign ↔ Tutorial/Tutorial 1 omic-to-image (spatial transcriptomics to CCF)/spatial transcriptomic section (Slide-seq_29) to Allen Brain Atlas.ipynb, lines 44–77 · score 0.64 · Allen Brain Atlas, Slide seq, SSI rendering, UMI, radius, filtered
  3. [3] § Results › SPOmiAlign enables registration of spatial omic sections to the common coordinate framework and anatomical annotation retrieval ↔ Tutorial/Tutorial 1 omic-to-image (spatial transcriptomics to CCF)/spatial transcriptomic section (Slide-seq_29) to Allen Brain Atlas.py, lines 56–75 · score 0.56 · Allen Brain Atlas, Slide seq, spatial transcriptomic, spot, CCF
  4. [4] § Methods › Differential analysis of multiomic data ↔ Flow2Spatial/model/utils.py, lines 216–273 · score 0.55 · AnnData, Scanpy, protein, gene, matrices, intensity
  5. [5] § Results › SPOmiAlign enables registration of spatial omic sections to the common coordinate framework and anatomical annotation retrieval ↔ Tutorial/Tutorial 1 omic-to-image (spatial transcriptomics to CCF)/spatial transcriptomic section (Slide-seq_29) to Allen Brain Atlas.ipynb, lines 1–42 · score 0.55 · Allen Brain Atlas, Slide seq, image alignment, spatial omics, SPOmiAlign
  6. [6] § Methods › Data preprocessing in SPOmiAlign ↔ Tutorial/Tutorial 1 omic-to-image (spatial transcriptomics to CCF)/spatial transcriptomic section (Slide-seq_29) to Allen Brain Atlas.ipynb, lines 44–77 · score 0.54 · spatial transcriptomic, manual rotation, UMI, SSI, radius, seq
  7. [7] § Methods › Data preprocessing in SPOmiAlign ↔ Tutorial/Tutorial 1 omic-to-image (spatial transcriptomics to CCF)/spatial transcriptomic section (Slide-seq_29) to Allen Brain Atlas.py, lines 56–75 · score 0.54 · Allen Brain Atlas, Slide seq, UMI, SSI, radius, spots
  8. [8] § Methods › Data preprocessing in SPOmiAlign ↔ SHARP-Track/Analyze_ROIs.m, lines 81–154 · score 0.52 · reference spaces, ROIs, sagittal, coronal, Allen, pixel

Paper

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The authors' code

Jupyter notebook · 144 lines · 4.8 KB · no license · 3 matches

  1. # %% [markdown]
  2. # # spatial transcriptomic section (Slide-seq_29) to Allen Brain Atlas
  3. #
  4. # This tutorial demonstrates omic-to-image alignment by registering the Slide-seq_29 spatial omics section to the Allen Brain Atlas image reference.
  5. #
  6. # Tutorial 1: spatial omics to CCF (omic-to-image)
  7. # %% [markdown]
  8. # ## 1. Load package and data paths
  9. # %%
  10. from pathlib import Path
  11. import sys
  12. import matplotlib.pyplot as plt
  13. import cv2
  14. try:
  15. START_DIR = Path(__file__).resolve().parent
  16. except NameError:
  17. START_DIR = Path.cwd()
  18. PROJECT_ROOT = next(
  19. candidate for candidate in (START_DIR, *START_DIR.parents)
  20. if (candidate / "SPOmiAlign").is_dir()
  21. )
  22. spomialign_path = PROJECT_ROOT / "SPOmiAlign"
  23. if str(spomialign_path) not in sys.path:
  24. sys.path.insert(0, str(spomialign_path))
  25. from tutorial_utils import (
  26. generate_ssi_visualization,
  27. get_tutorial_paths,
  28. run_omic_to_image_alignment,
  29. read_bgr,
  30. )
  31. DATA_DIR, OUTPUT_ROOT = get_tutorial_paths(PROJECT_ROOT)
  32. SAMPLE_ID = "PUCK29"
  33. SOURCE_OMIC_PATH = "Tutorial 1 spatial omics to CCF (omic-to-image)/Puck_Num_29.h5ad"
  34. TARGET_IMAGE_PATH = "Tutorial 1 spatial omics to CCF (omic-to-image)/CCF_100048576_205.png"
  35. SSI_IMAGE_PATH = None
  36. %matplotlib inline
  37. # %% [markdown]
  38. # ## 2. Parameter settings
  39. #
  40. # | Parameter | Meaning |
  41. # | --- | --- |
  42. # | `SAMPLE_ID` | Output folder name under `output/h5ad_2_img/`. |
  43. # | `SOURCE_OMIC_PATH` | Source spatial omics h5ad path in data. |
  44. # | `TARGET_IMAGE_PATH` | Reference image path in data. |
  45. # | `SSI_IMAGE_PATH` | The path of rendered SSI image. |
  46. # | `manual_rotate` | Clockwise manual rotation applied when rendering the source h5ad into SSI. |
  47. # | `SSI_dpi` | SSI rendering resolution. The default value is 150. |
  48. # | `x_coordinate` / `y_coordinate` | Spot coordinate columns used for SSI rendering. |
  49. # | `SPOT_UMI` | UMI is calculated by default; use this h5ad obs key if available. |
  50. # | `threshold_percentile` | Optional intensity(UMI) percentile filter; `None` keeps all valid spots. |
  51. # | `SPOT` | Spot shape (`square` / `circle`) and visualization radius. |
  52. # | `Alignment_mode` | SPOmiAlign supports three alignment modes: Rigid (`Rigid`), Affine (`Affine`, `Homography`), and Non-Rigid (`bspline`, `affine+bspline`). |
  53. # | `device` | Torch device used by alignment, for example `cuda:0`, `cuda:1`, or `cpu`; `None` keeps automatic selection. |
  54. # %%
  55. SSI_PARAMS = {
  56. "manual_rotate": 180,
  57. "SSI_dpi": 150,
  58. "x_coordinate": "Raw_Slideseq_X",
  59. "y_coordinate": "Raw_Slideseq_Y",
  60. "SPOT_UMI": "nFeature_Spatial",
  61. "threshold_percentile": 80,
  62. "SPOT": {"shape": "circle", "radius": 5},
  63. }
  64. ALIGNMENT_PARAMS = {
  65. "Alignment_mode": "affine+bspline",
  66. "device": "cuda:0",
  67. }
  68. SAMPLE_ID, SOURCE_OMIC_PATH, TARGET_IMAGE_PATH, SSI_IMAGE_PATH, SSI_PARAMS, ALIGNMENT_PARAMS
  69. # %% [markdown]
  70. # ## 3. Generate SSI image
  71. #
  72. # The SSI image is generated from the spatial omics h5ad before alignment. For these Slide-seq examples, spot coordinates are read from `Raw_Slideseq_X` and `Raw_Slideseq_Y`, and spot intensity is read from `nFeature_Spatial`.
  73. # %%
  74. ssi = generate_ssi_visualization(
  75. data_root=DATA_DIR,
  76. output_root=OUTPUT_ROOT,
  77. sample_id=SAMPLE_ID,
  78. source_omic_path=SOURCE_OMIC_PATH,
  79. **SSI_PARAMS,
  80. )
  81. images=[ssi["source_section_visualization"]]
  82. titles=["Generated SSI"]
  83. figsize=(6, 6)
  84. titles = titles or ["" for _ in images]
  85. if figsize is None:
  86. figsize = (5.5 * len(images), 5.5)
  87. fig, axes = plt.subplots(1, len(images), figsize=figsize)
  88. if len(images) == 1:
  89. axes = [axes]
  90. for ax, image_or_path, title in zip(axes, images, titles):
  91. image = read_bgr(image_or_path) if isinstance(image_or_path, (str, Path)) else image_or_path
  92. ax.imshow(cv2.cvtColor(image, cv2.COLOR_BGR2RGB))
  93. ax.set_title(title)
  94. ax.axis("off")
  95. plt.tight_layout()
  96. plt.show()
  97. # %% [markdown]
  98. # ## 4. Run SPOmiAlign
  99. # %%
  100. result = run_omic_to_image_alignment(
  101. data_root=DATA_DIR,
  102. output_root=OUTPUT_ROOT,
  103. sample_id=SAMPLE_ID,
  104. source_omic_path=SOURCE_OMIC_PATH,
  105. target_image_path=TARGET_IMAGE_PATH,
  106. SSI_IMAGE_PATH=SSI_IMAGE_PATH,
  107. **SSI_PARAMS,
  108. **ALIGNMENT_PARAMS,
  109. )
  110. # %% [markdown]
  111. # ## 5. Outputs
  112. # %%
  113. images=[result["source_section_visualization"], result["target_section_visualization"], result["overlay"]]
  114. titles=["Generated SSI", "CCF reference", "Aligned slice overlay"]
  115. figsize=(6, 6)
  116. titles = titles or ["" for _ in images]
  117. if figsize is None:
  118. figsize = (5.5 * len(images), 5.5)
  119. fig, axes = plt.subplots(1, len(images), figsize=figsize)
  120. if len(images) == 1:
  121. axes = [axes]
  122. for ax, image_or_path, title in zip(axes, images, titles):
  123. image = read_bgr(image_or_path) if isinstance(image_or_path, (str, Path)) else image_or_path
  124. ax.imshow(cv2.cvtColor(image, cv2.COLOR_BGR2RGB))
  125. ax.set_title(title)
  126. ax.axis("off")
  127. plt.tight_layout()
  128. plt.show()
  129. print("Save transformed h5ad path to ", result["transformed_h5ad"])

spatial transcriptomic section (Slide-seq_29) to Allen Brain Atlas.ipynb at commit c7f8b7a, no license · at the source

Overview

Authors: Yi Wang1,2, Zihang He3, Yunjie Yan4
ORCID iDs: Yi Wang, Zihang He
  1. Liangzhu Laboratory, Zhejiang University School of Medicine, No. 1369 Wenyi West Road, Yuhang District, Hangzhou, Zhejiang Province 311113, China
  2. Zhejiang Key Laboratory of Multi-Omics in Infection and Immunity, Center for Infectious Disease Research, School of Medicine, Westlake University, No. 18 Shilongshan Street, Zhuantang Subdistrict, Xihu District, Hangzhou, Zhejiang Province 310024, China
  3. Zhejiang University-University of Edinburgh Institute (ZJE), Zhejiang University School of Medicine, Zhejiang University, 718 East Haizhou Road, Haining, 314400, China
  4. Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University, 3 East Qingchun Road, Hangzhou, 310016, China
Journal: Briefings in bioinformatics, volume 27, issue 3, article bbag331
Dates: received 21 February 2026; accepted 24 May 2026; published online 21 June 2026; in print May 2026
Type: Research article · Language: English
License: CC BY
Identifiers: DOI 10.1093/bib/bbag331 · PMID 42323879 · PMCID PMC13283438 · OpenAlex W7165478251
Open access: gold, a free copy (OpenAlex)
Status: code verified
Categories: genetics / omics (modality), mouse (organism), methods / tools (subfield)
Methods: Statistics, Smoothing, state filtering, decompositions, Connectivity, Machine learning, fMRI & imaging, Spectral & time-frequency
Keywords: spatial multimodal alignment, feature matching, foundation model, common coordinate framework, spatial multi-omics integration
MeSH: Computational Biology*, Proteomics*, Software*, Algorithms, Animals, Brain, Metabolomics, Mice, Multiomics, Spatial Transcriptomics (* major topic)
Topic: Single-cell and spatial transcriptomics (Molecular Biology, Biochemistry, Genetics and Molecular Biology), according to OpenAlex
Funding: National Key Research and Development Program of China (2024YFA1306600); Yuhang District Postdoctoral Research Funding Program
Citations: not cited yet (Europe PMC); 47 references in the paper

Abstract

Multimodal spatial omics enables systematic characterization of tissue organization by jointly profiling transcriptomic, proteomic, metabolomic, and other spatially resolved modalities within their spatial context. A central challenge in realizing this potential is achieving robust spatial alignment across modalities and sections. Although numerous alignment methods have been developed, most are designed for single-modality sections or specific modality combinations, with few enabling modality-agnostic alignment. Cross-modal alignment remains difficult due to the absence of shared molecular features, partial spatial overlap, and nonrigid tissue deformations. To address these challenges, we introduce SPOmiAlign, a modality-agnostic framework for spatial multimodal alignment, enabled by a feature-matching foundation model that serves as a general computational primitive for spatial multi-omics alignment. The framework enables accurate cross-modal spatial alignment without manual intervention or modality-specific tuning. Across diverse multimodal benchmarks, SPOmiAlign consistently achieves higher alignment accuracy than existing methods. We further demonstrate its utility through automated registration to a common coordinate framework, enabling standardized anatomical annotation. Finally, applying SPOmiAlign to integrate spatial transcriptomic, proteomic, and metabolomic data in mouse brain facilitates the identification of spatial domains that were difficult to resolve with less accurate registration, highlighting its utility for multi-omic integration and biological interpretation.

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

Repositories

Its files are read in the Code ↔ Paper reader above, with 8 matches between paragraphs and lines of code.

cortex-lab/allenccf

License: none: the authors keep all their rights
State: the link answers, verified on 27 September 2026
Evidence: files inventoried
Commit: e5a57fe7e1c9fb333fec51c29a8471131c233a76, 15 July 2025
Languages: MATLAB (61)
Size: 75 files, 61 scripts
Software Heritage: not archived
Found in: “Data availability”
Holds: README
Not found: license file, CITATION.cff, environment file, tests, continuous integration, documentation
Availability: 1 check, the latest on 27 September 2026: the link answers
  • 27 September 2026: the link answers
62 files

gpenglab/misar-seq

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State: the link answers, verified on 27 September 2026
Evidence: files inventoried
Commit: 6fdceee0aa05e85473bbde84eeafdee5af7f8a9f, 4 September 2026
Languages: R (5), Python (4), Shell (1)
Size: 26 files, 10 scripts
Software Heritage: not checked
Found in: “Data availability”
Holds: README
Not found: license file, CITATION.cff, environment file, tests, continuous integration, documentation
Tools: tidyverse (4 files), Biopython (2 files), clusterProfiler (2 files), igraph (2 files), NumPy (2 files), patchwork (2 files), reticulate (2 files), Seurat (2 files), deepTools (1 file), Matplotlib (1 file), Numba (1 file), OpenCV (1 file), pandas (1 file), Scanpy (1 file), SciPy (1 file)
Availability: 1 check, the latest on 27 September 2026: the link answers
  • 27 September 2026: the link answers
11 files

bioinfo-biols/flow2spatial

License: GPL-3.0
State: the link answers, verified on 27 September 2026
Evidence: files inventoried
Commit: 4ce25791e904dafb677ae93fa052b0acfb75ac91, 16 May 2025
Languages: Python (11)
Size: 36 files, 11 scripts
Software Heritage: not archived
Found in: “Data availability”
Holds: README, license file, environment (setup.py, docs/requirements.txt), documentation
Not found: CITATION.cff, tests, continuous integration
Tools: NumPy (4 files), pandas (4 files), anndata (2 files), Matplotlib (2 files), SciPy (2 files), PyTorch (1 file), scikit-image (1 file)
Availability: 1 check, the latest on 27 September 2026: the link answers
  • 27 September 2026: the link answers
13 files

wangyiyuyang/SPOmiAlign

License: none: the authors keep all their rights
State: the link answers, verified on 27 September 2026
Evidence: files inventoried
Commit: c7f8b7adeddcbd9c67683e6f9edfd40153b2ea5b, 15 May 2026
Languages: Python (70), Jupyter (4), C++ (1), CUDA (1)
Size: 132 files, 76 scripts
Software Heritage: not checked
Found in: “Data availability”
Holds: README, environment (SPOmiAlign/software/Roma/pyproject.toml, SPOmiAlign/software/Roma/requirements.txt, SPOmiAlign/software/Roma/uv.lock, SPOmiAlign/software/fused-local-corr-master/fused-local-corr-master/pyproject.toml, SPOmiAlign/software/fused-local-corr-master/fused-local-corr-master/requirements.txt, SPOmiAlign/software/fused-local-corr-master/fused-local-corr-master/setup.py), tests, documentation, 4 notebooks
Not found: license file, CITATION.cff, continuous integration
Tools: PyTorch (47 files), NumPy (23 files), Pillow (19 files), OpenCV (18 files), Matplotlib (14 files), Scanpy (5 files), pandas (4 files), SciPy (4 files), h5py (2 files), anndata (1 file), scikit-image (1 file), SimpleITK (1 file)
Availability: 1 check, the latest on 27 September 2026: the link answers
  • 27 September 2026: the link answers
77 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:

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

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Data

Datasets cited

Data availability

All datasets used in this study are publicly available. The Slide-seq dataset, a high-throughput sequencing-based spatial transcriptomics technology with near-cellular resolution comprising 101 adult mouse brain coronal sections that span the entire anteroposterior axis, was obtained from an online resource at https://docs.braincelldata.org/downloads/index.html/Slide-seq_Data. The MERFISH dataset, a high-throughput imaging-based spatial transcriptomics technology with single-cell resolution consisting of 25 adult mouse brain sagittal sections, was obtained from the Allen Brain Cell Atlas at https://alleninstitute.github.io/abc_atlas_access/descriptions/Zhuang-ABCA-3.html. The Allen Common Coordinate Framework (CCF) and the corresponding brain region annotations were obtained from the Allen Brain Atlas. Nissl-stained reference images of the adult mouse brain CCF used for alignment are publicly available for coronal views at https://mouse.brain-map.org/experiment/thumbnails/100048576?image_type=atlas and sagittal views at https://mouse.brain-map.org/experiment/thumbnails/100042147?image_type=atlas. Brain region annotations corresponding to the 25 m resolution CCF were downloaded from the file annotation_25.nrrd at https://download.alleninstitute.org/informatics-archive/current-release/mouse_ccf/annotation/ccf_2017/annotation_25.nrrd. The correspondence between the brain region identifiers and the anatomical labels was obtained from structure _tree _safe _2017.csv, available at https://github.com/cortex-lab/allenCCF/blob/master/structure_tree_safe_2017.csv. The MISAR-seq dataset, a spatial multiomic profiling dataset of the mouse brain that jointly measures chromatin accessibility and gene expression, was obtained from a public repository at https://github.com/gpenglab/MISAR-seq/blob/main/Data/Download. The cRCC R114 dataset used in this study, including the spatial transcriptomics and MALDI imaging mass spectrometry-based metabolomics data, was obtained from a public repository at https://zenodo.org/records/14986870. The spatial multiomic mouse brain dataset that integrates MALDI imaging mass spectrometry-based metabolomics, MAGIC-seq spatial transcriptomics, and PLATO spatial proteomics was obtained from a public repository at https://github.com/bioinfo-biols/Flow2Spatial/tree/main/datasets. Source data are provided with this paper. The code for the SPOmiAlign program is available on GitHub at https://github.com/wangyiyuyang/SPOmiAlign. All source code will be released publicly once the manuscript is published.

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

Versions

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Version 1, 27 September 2026: the first record

Recorded: type, language, journal, volume, issue, pages, dates, 3 authors, 5 keywords, 10 MeSH terms, 2 funders, 42 references.

Cite

This paper

Wang, Y., He, Z., & Yan, Y. (2026). SPOmiAlign: a modality-agnostic computational framework for multimodal spatial omics alignment enabled by a feature matching foundation model. Briefings in bioinformatics, 27(3), bbag331. https://doi.org/10.1093/bib/bbag331

BibTeX

@article{wang2026spomialign,
author = {Wang, Yi and He, Zihang and Yan, Yunjie},
title = {{SPOmiAlign: a modality-agnostic computational framework for multimodal spatial omics alignment enabled by a feature matching foundation model}},
journal = {Briefings in bioinformatics},
year = {2026},
month = may,
volume = {27},
number = {3},
pages = {bbag331},
publisher = {Oxford University Press},
issn = {1467-5463},
doi = {10.1093/bib/bbag331},
url = {https://doi.org/10.1093/bib/bbag331},
pmid = {42323879},
pmcid = {PMC13283438}
}

RIS

TY - JOUR
AU - Wang, Yi
AU - He, Zihang
AU - Yan, Yunjie
TI - SPOmiAlign: a modality-agnostic computational framework for multimodal spatial omics alignment enabled by a feature matching foundation model
T2 - Briefings in bioinformatics
J2 - Brief Bioinform
PY - 2026
DA - 2026/05/01
VL - 27
IS - 3
SP - bbag331
SN - 1467-5463
PB - Oxford University Press
DO - 10.1093/bib/bbag331
UR - https://doi.org/10.1093/bib/bbag331
LA - en
ER -

CSL-JSON

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