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Campbell, D. R.

Publications and source records attributed to Campbell, D. R..

3 recordsLinked to original sources

Atacformer: A transformer-based foundation model for analysis and interpretation of ATAC-seq data

IntroductionChromatin accessibility profiling is an important tool for understanding gene regulation and cellular function. While public repositories house nearly 10,000 scATAC-seq experiments, unifying this data for meaningful analysis remains challenging. Existing tools struggle with the scale and complexity of scATAC-seq datasets, limiting tasks like clustering, cell-type annotation, and reference mapping. A promising solution is using foundation models adapted to specific tasks via transfer learning. While transfer learning has been applied to scRNA-seq, its potential for scATAC-seq remains underexplored. MethodsWe introduce Atacformer, a transformer-based foundation model for scATAC-seq data analysis. Unlike other models that only produce cell-level representations, Atacformer generates embeddings for individual cis-regulatory elements. Pre-trained on a large atlas of scATAC-seq experiments, Atacformer learns robust representations of genomic regulatory regions for downstream use. After pretraining, the model is fine-tuned for cell-type prediction and batch correction. We also integrated Atacformer with RNA-seq data to build a Contrastive RNA-ATAC Fine Tuning (CRAFT) model capable of cross-modal alignment and RNA imputation from ATAC data. ResultsAtacformer matches or exceeds leading scATAC-seq clustering tools in adjusted rand index and runtime, with fine-tuned models achieving top performance across datasets. It processes raw fragment files end-to-end 80% faster than existing tools while preserving biological structure. Fine-tuned on bulk BED files, it recovers cell type and assay labels with >80% accuracy. We show how the Atacformer architecture produces contextualized embeddings of individual genomic regions, which we use to identify unannotated, cell-type-specific promoter elements directly from chromatin accessibility data.

bioinformatics↗

Taming the reference genome jungle: the refget sequence collection standard

Reference genomes are foundational to genomics but suffer from widespread ambiguity and incompatibility due to inconsistent naming, undocumented differences, and lack of formal mechanisms for comparison. To address this, we introduce the GA4GH refget Sequence Collections (seqcol) standard. Refget seqcol is a framework for unambiguous representation, retrieval, and comparison of sequence collections such as reference genomes and transcriptomes. The seqcol standard comprises four components: a structured data schema, a canonical encoding algorithm that produces content-based, globally unique identifiers, a retrieval API, and a comparison protocol. This standard enables precise identification of sequence collections, even across decentralized or private systems, and allows compatibility assessments beyond exact identity, such as order-relaxed matches or shared coordinate systems. We applied the refget seqcol standard to 60 human and 36 mouse reference genomes sourced from major providers. Using digest-based comparisons, we quantified levels of similarity across attributes including sequence names, lengths, coordinate systems, and actual sequence content. Our analysis revealed some consistent subsets of sequences or coordinate systems, as well as substantial incompatibility among references and duplicate references under different names. To support adoption of refget seqcol, we provide a Python package implementing the full standard, a web API, and a comparison interface allowing users to assess local references against a curated database. This work offers a scalable, reproducible solution to the reference genome compatibility crisis, enabling improved transparency, reuse, and integration in genomic analyses. Refget seqcol enhances interoperability across tools and datasets, making genomic research more robust and reproducible.

genomics↗

BEDMS: A metadata standardizer for genomic regionattributes

High-throughput sequencing technologies have generated vast omics data annotating genomic regions. A challenge arises in integrating this data because the associated metadata does not follow a uniform schema. This hinders data management, discovery, interoperability, and reusability. Existing tools that address metadata standardization issues are generally limited in scope and targeted toward specific data sets or types and are not generally applicable to custom schemas. To improve standardization of genomic interval metadata, we have developed BEDMS. We developed and evaluated several model architectures and trained models that achieved high performance on held-out training data. With a trained model, BEDMS provides users with predicted standardized metadata attributes that follow a standardized schema. Furthermore, BEDMS provides the ability to train custom models. To demonstrate, we trained BEDMS on three different schemas, allowing users to choose which schema to standardize into. We also deployed BEDMS on PEPhub, which provides a graphical user interface to allow users to standardize metadata without requiring any local training or software at all. In conclusion, BEDMS offers a practical one-stop solution for metadata management and standardization for genomic interval data.

genomics↗