Evidence map›Paper›PMID 41752025›Full record

ArticleInternational journal of molecular sciences2026

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

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

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Courtney L HallDepartment of Biomedical Engineering, Johns Hopkins University, 3400 N Charles St., Baltimore, MD 21201, USA.
Rupesh K KesharwaniDepartment of Neurology, The University of Texas Health Science Center at Houston, 7000 Fannin St., Houston, TX 77030, USA.ORCID 0000-0002-4678-5419
Katherine E McBroom HensonDepartment of Microbiology, Immunology & Genetics, University of North Texas Health Science Center, 3500 Camp Bowie Blvd., Fort Worth, TX 76107, USA.ORCID 0009-0009-4554-534X
Bupe KapemaDepartment of Microbiology, Immunology & Genetics, University of North Texas Health Science Center, 3500 Camp Bowie Blvd., Fort Worth, TX 76107, USA.
Nicole R PhillipsDepartment of Microbiology, Immunology & Genetics, University of North Texas Health Science Center, 3500 Camp Bowie Blvd., Fort Worth, TX 76107, USA.
Fritz J SedlazeckDepartment of Neurology, The University of Texas Health Science Center at Houston, 7000 Fannin St., Houston, TX 77030, USA.
Roxanne R ZascavageDepartment of Microbiology, Immunology & Genetics, University of North Texas Health Science Center, 3500 Camp Bowie Blvd., Fort Worth, TX 76107, USA.ORCID 0000-0002-2878-0737

Funding

National Institute of Justice 15PNIJ-22-GG-04414-MUMUNational Institute of Justice 2018-DU-BX-0179
6 · The paper itself

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.

Indexed as

DNA FingerprintingForensic GeneticsMicrosatellite RepeatsNanopore SequencingSequence Analysis, DNASoftwareChromosomes, Human, YHigh-Throughput Nucleotide SequencingHumansbioinformaticsDNA sequencinghuman identificationnanopore sequencingshort tandem repeatsSTRspy

Identifiers

PMID41752025
PMCPMC12940929

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.