# Modular strategies for spatial mapping of diverse cell type data of the mouse brain

**Authors:** Nicholas J. Tustison, Min Chen, Fae N. Kronman, Jeffrey T. Duda, Clare Gamlin, Mia G. Tustison, Michael Kunst, Rachel Dalley, Staci Sorenson, Quanxin Wang, Lydia Ng, Yongsoo Kim, James C. Gee

PMC · DOI: 10.21203/rs.3.rs-6289741/v1 · Research Square · 2025-04-09

## TL;DR

This paper presents modular strategies for mapping diverse mouse brain cell type data into common spatial frameworks, enabling joint analysis across different data types.

## Contribution

The work introduces novel open-source mapping strategies tailored to specific data types and publicly available through ANTSX.

## Key findings

- Velocity flow-based approaches enable continuous mapping of developmental trajectories into the DevCCF.
- An automated framework leverages public resources to determine structural morphology without specialized software.
- Modular strategies are adaptable to unique data challenges without requiring new software development.

## Abstract

Large-scale, international collaborative efforts by members of the BRAIN Initiative Cell Census Network (BICCN) consortium are aggregating the most comprehensive reference database to date for diverse cell type profiling of the mouse brain, which encompasses over 40 different multi-modal profiling techniques from more than 30 research groups. One central challenge for this integrative effort has been the need to map these unique datasets into common reference spaces such that the spatial, structural, and functional information from different cell types can be jointly analyzed. However, significant variation in the acquisition, tissue processing, and imaging techniques across data types makes mapping such diverse data a multifarious problem. Different data types exhibit unique tissue distortion and signal characteristics that precludes a single mapping strategy from being generally applicable across all cell type data. Tailored mapping approaches are often needed to address the unique barriers present in each modality. This work highlights modular atlas mapping strategies developed across separate BICCN studies using the Advanced Normalization Tools Ecosystem (ANTsX) to map spatial transcriptomic (MERFISH) and high-resolution morphology (fMOST) mouse brain data into the Allen Common Coordinate Framework (AllenCCFv3), and developmental (MRI and LSFM) data into the Developmental Common Coordinate Framework (DevCCF). We discuss common mapping strategies that can be shared across modalities and driven by specific challenges from each data type. These mapping strategies include novel open-source contributions that are made publicly available through ANTSX. These include 1) a velocity flow-based approach for continuously mapping developmental trajectories such as that characterizing the DevCCF and 2) an automated framework for determining structural morphology solely through the leveraging of publicly resources. Finally, we provide general guidance to aid investigators to tailor these strategies to address unique data challenges without the need to develop additional specialized software.

## Linked entities

- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Species:** Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12036443/full.md

## References

89 references — full list in the complete paper: https://tomesphere.com/paper/PMC12036443/full.md

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Source: https://tomesphere.com/paper/PMC12036443