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Updated: Feb 28, 2026

Ultra-long Read Sequencing for Whole Genomic DNA Analysis
Published on: March 15, 2019
STRspy2.0: Unlocking the Potential of Long Reads for Forensic DNA Profiling
Courtney L Hall1, Rupesh K Kesharwani2,3, Katherine E McBroom Henson4
1Department of Biomedical Engineering, Johns Hopkins University, 3400 N Charles St., Baltimore, MD 21201, USA.
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.

