STRspy2.0: Unlocking the Potential of Long Reads for Forensic DNA Profiling

Forensic human identification relies on length-based differences in short tandem repeats (STRs) across autosomal and Y chromosomes, which require separate reactions and provide limited resolution. While next-generation sequencing offers greater discriminatory power, most platforms are expensive and restricted to traditional lab settings. Nanopore sequencing has the potential to change this with the real-time, portable MinION sequencer. However, forensic-specific tools that generate STR profiles compatible with established length-based databases are lacking. To address this, we developed STRspy2.0, which simultaneously profiles autosomal and Y-STRs using nanopore reads. STRspy2.0 produced accurate profiles for 54 multiplexed control libraries and 41 mock casework samples (blood, swab, bone), achieving overall F1-scores of 100% and 99.75%, respectively. It maintains compatibility with existing forensic databases while providing higher resolution than traditional profiles. Our updated method and comprehensive database, along with the MinION's small size and price, make sequence-based STR profiling more accessible to forensic laboratories and resource-limited settings.

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Publication Details

Journal
International Journal of Molecular Sciences
Published
2026-02-16
DOI
https://doi.org/10.3390/ijms27041889
Primary Topic
Forensic and Genetic Research
Type
article
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article

STRspy2.0: Unlocking the Potential of Long Reads for Forensic DNA Profiling

Courtney Hall, Bupe Kapema, Katherine E. McBroom Henson, Roxanne R. Zascavage et al.
International Journal of Molecular Sciences
Forensic and Genetic Research
article

STRspy2.0: Unlocking the Potential of Long Reads for Forensic DNA Profiling

Courtney Hall, Bupe Kapema, Katherine E. McBroom Henson, Roxanne R. Zascavage, Fritz J. Sedlazeck, Nicole R. Phillips, Rupesh K. Kesharwani
article en

Abstract

Forensic human identification relies on length-based differences in short tandem repeats (STRs) across autosomal and Y chromosomes, which require separate reactions and provide limited resolution. While next-generation sequencing offers greater discriminatory power, most platforms are expensive and restricted to traditional lab settings. Nanopore sequencing has the potential to change this with the real-time, portable MinION sequencer. However, forensic-specific tools that generate STR profiles compatible with established length-based databases are lacking. To address this, we developed STRspy2.0, which simultaneously profiles autosomal and Y-STRs using nanopore reads. STRspy2.0 produced accurate profiles for 54 multiplexed control libraries and 41 mock casework samples (blood, swab, bone), achieving overall F1-scores of 100% and 99.75%, respectively. It maintains compatibility with existing forensic databases while providing higher resolution than traditional profiles. Our updated method and comprehensive database, along with the MinION's small size and price, make sequence-based STR profiling more accessible to forensic laboratories and resource-limited settings.

International Journal of Molecular SciencesVol. 27(4)
University of North Texas (US), Johns Hopkins University (US), University of North Texas Health Science Center (US), Baylor College of Medicine (US), The University of Texas Health Science Center (US), University of Baltimore (US), Rice University (US), The University of Texas Health Science Center at Houston (US)
Reduced inequalities
Openalex Percentile: Top 51%
Forensic and Genetic Research
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STRspy2.0: Unlocking the Potential of Long Reads for Forensic DNA Profiling — Courtney Hall, Bupe Kapema, et al. · International Journal of Molecular Sciences (2026) | TGRS Research Map | TGRS