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A Community Standard Multispecies Cell Atlas of the Basal Ganglia
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A Community Standard Multispecies Cell Atlas of the Basal Ganglia

The BRAIN Initiative Cell Atlas Network (BICAN), Joseph R. Ecker, Michael Hawrylycz +6 more
April 2026
 ·
bioRxiv
 ·
DOI 
10.64898/2026.04.14.717814
94
%
Reproducible
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It ranks in the top 1% of preprints assessed in Neuroscience this quarter.
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Why this is interesting

By creating the first cross-species multimodal atlas of the basal ganglia—spanning human to mouse with unified ontologies and open tools—this work transforms comparative neuroanatomy from a fragmented endeavor into a scalable, disease-ready reference platform.

QED claims analysis

Summary

The BRAIN Initiative Cell Atlas Network established a foundational, cross-species cell atlas of the mammalian basal ganglia by integrating single-nucleus transcriptomic data from over 17.4 million cells across human, macaque, marmoset, and mouse into a unified taxonomy with standardized nomenclature, anchored to harmonized anatomical reference frameworks and supported by a comprehensive FAIR ecosystem of standardized sequencing pipelines, data infrastructure, and community tools that enables reproducible brain cell type classification and serves as a scalable model for whole-brain atlas generation.

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Main Claim 1 –

Cross-species basal ganglia taxonomy from snRNA-seq in four mammals

Supporting evidence

  • HOMBA and common coordinate frameworks anchor cross-species taxonomy anatomically
  • Taxonomy based on 17.4M multimodally profiled basal ganglia cells
  • Taxonomy validated via multimodal development, disease studies, and genetic tools
Main Claim 2 –

BICAN FAIR ecosystem standardizes pipelines, infrastructure, tools, and metadata

Supporting evidence

  • Standardized workflows and NIMP platform operationalize ecosystem integration
  • BICAN tools enable community visualization, analysis, and cell-type mapping
  • Standardized donor programs ensure high-quality, ethically stewarded biospecimens

Abstract

The NIH BRAIN Initiative Cell Atlas Network (BICAN) aims to generate a standardized, integrated cell atlas of the human, macaque, marmoset, and mouse brain that serves as a foundational community reference for the classification and study of brain cell types. Here we present the first major component of this effort: a cross-species, multimodal atlas of the basal ganglia, a group of subcortical nuclei central to motor control and implicated in a broad range of neurological disorders. Grounded in large-scale single-cell transcriptomic classification and integrated with epigenomic and spatial genomic modalities, this resource is enabled by coordinated cross-species sampling and harmonized analytical frameworks. It provides extensive phenotypic characterization of cell types, incorporates community-informed annotation, and establishes a highly curated, data-driven taxonomy with standardized nomenclature. The atlas is anchored to species-specific anatomical reference frameworks and linked across species through unified structural ontologies, enabling consistent cross-species comparisons. Multiple complementary datasets are mapped to this reference, including multiomic profiles and developmental trajectories aligned to adult cell states. Realization of this resource has required coordinated standards for tissue processing across human and model organisms, harmonization of donor metadata across brain banks, and the development of unified anatomical reference systems. To support these advances, BICAN has established an integrated ecosystem comprising standardized sequencing pipelines, neuroanatomically grounded data infrastructure, scalable visualization and mapping tools, and interoperable metadata standards. Analogous to the standardization achieved in genome science, this ecosystem provides a FAIR (findable, accessible, interoperable, and reusable) framework that enables researchers to map, compare, and interpret diverse datasets against a shared reference and associated knowledge base. The BICAN reference system is now being extended to the whole brain, with principles that are readily generalizable to other organ systems.

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