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---
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license:
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---
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license: mit
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tags:
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- neuroscience
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- genomics
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- dna
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- sequence-modeling
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- basal-ganglia
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- spinal-cord
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- astrocyte
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- regulatory-genomics
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pretty_name: DNA Sequence Modeling for BG Cell Atlas Package
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---
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# DNA Sequence Modeling for the Basal Ganglia Cell Atlas Package
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This repository contains DNA-sequence modeling resources associated with the basal ganglia (BG) cell atlas package. It serves as a centralized entry point for sequence-based regulatory analyses across multiple companion studies.
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## What this repository is
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This repository is a landing page and resource hub for DNA-sequence modeling analyses associated with the basal ganglia cell atlas package.
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## What this repository is not
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This repository is not intended to duplicate the full analysis pipelines of the companion studies. Instead, it provides a centralized entry point for sequence-modeling-related resources, outputs, and links.
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## Overview
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Across these studies, sequence-based modeling is used to investigate cis-regulatory logic underlying cell type specialization. These analyses complement multiomic profiling (snRNA-seq, snATAC-seq, spatial transcriptomics, methylation, and chromatin conformation) by providing a sequence-level perspective on candidate enhancers and regulatory programs.
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## Associated studies
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### 1. Basal ganglia consensus taxonomy
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**Johansen, Fu et al., 2025**
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This study establishes a consensus basal ganglia taxonomy by integrating HMBA single-nucleus RNA-seq data from human, macaque, marmoset, and previously published mouse datasets. The resulting framework provides a standardized naming system for basal ganglia cell types, enabling cross-species comparison, community-wide adoption, and downstream tool development.
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### 2. Cross-species spinal cord atlas
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**Schmitz, Johansen et al., 2026**
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This study presents a unified cross-species atlas integrating single-nucleus multiomic profiling and spatial transcriptomics across human, macaque, and mouse. In addition to defining a conserved cell type hierarchy, it links molecular identities to anatomical organization and cis-regulatory programs, including sequence-based modeling of enhancer logic.
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### 3. Human BG astrocyte subgroup study
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**Fu et al., 2026**
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This study identifies three major astrocyte subgroups in the human basal ganglia and characterizes their spatial, molecular, and regulatory specialization. Sequence-based modeling is used to evaluate subgroup-associated regulatory elements and candidate enhancer programs.
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## Repository contents
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Depending on the final organization, this repository include:
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- model configuration files
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- input sequence sets (candidate regulatory regions)
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- cell type-enriched regions
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- model predictions and scoring outputs
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- motif and enhancer-level summaries
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- example loci used in the manuscript
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## Conceptual workflow
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1. Define candidate regulatory regions from multiomic data
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2. Extract DNA sequences for modeling
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3. Train or apply sequence-based models
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4. Score sequences for regulatory activity
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5. Interpret subgroup- or cell type-specific regulatory patterns
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## Links
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- Basal ganglia consensus taxonomy paper: [add link]
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- Spinal cord consensus atlas paper: [add link]
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- Basal ganglia astrocyte study: [add link]
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- Multiomic track viewer (SCMDAP): [add link]
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- Project GitHub repository: [add link]
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## Citation
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Please cite the relevant companion manuscripts when using these resources.
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@article{BG_PACKAGE,
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title = {Cross-species consensus atlas of the primate basal ganglia},
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author = {Johansen, Nelson and Fu, Yuanyuan and others},
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journal = {bioRxiv},
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year = {2025}
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}
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@article{BG_PACKAGE,
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title = {A consensus spinal cord cell type atlas across mouse, macaque, and human},
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author = {Schmitz, Matthew and Johansen, Nelson and others},
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journal = {bioRxiv},
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year = {2026}
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}
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@article{BG_PACKAGE,
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title = {Circuit-dependent specialization of human basal ganglia astrocytes},
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author = {Fu, Yuanyuan and others},
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journal = {bioRxiv},
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year = {2025}
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}
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