Evidence map›Paper›PMID 42624859›Full record

ArticleScientific reports2026

MARLOWE: taxonomic characterization of unknown samples for forensics using de novo peptide identification.

Sarah C Jenson, Fanny Chu, Gelio Alves, Aleksey Y Ogurtsov, Anthony S Barente, Dustin L Crockett, Natalie C Lamar, Eric D Merkley, Yi-Kuo Yu, Kristin H Jarman

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In one paragraph

Article in Scientific reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Sarah C Jenson *Chemical and Biological Signatures Group, Pacific Northwest National Laboratory, Richland, WA, 99352, USA.
Fanny Chu *Chemical and Biological Signatures Group, Pacific Northwest National Laboratory, Richland, WA, 99352, USA. fanny.chu@pnnl.gov.
Gelio AlvesDivision of Intramural Research, National Library of Medicine, National Institutes of Health, Bethesda, MD, 20854, USA.
Aleksey Y OgurtsovDivision of Intramural Research, National Library of Medicine, National Institutes of Health, Bethesda, MD, 20854, USA.
Anthony S BarenteChemical and Biological Signatures Group, Pacific Northwest National Laboratory, Richland, WA, 99352, USA.
Dustin L CrockettApplied Decisions Systems and Analytics, Group, Pacific Northwest National Laboratory, Richland, WA, 99352, USA.
Natalie C LamarApplied Statistics and Computational Modeling Group, Pacific Northwest National Laboratory, Richland, WA, 99352, USA.
Eric D MerkleyChemical and Biological Signatures Group, Pacific Northwest National Laboratory, Richland, WA, 99352, USA.
Yi-Kuo YuDivision of Intramural Research, National Library of Medicine, National Institutes of Health, Bethesda, MD, 20854, USA.
Kristin H JarmanChemical and Biological Signatures Group, Pacific Northwest National Laboratory, Richland, WA, 99352, USA.

Funding

U.S. Department of Homeland Security HSHQPM16X00216
6 · The paper itself

Abstract

We present a computational tool, MARLOWE, for source organism characterization of unknown, forensic biological samples. The intent of MARLOWE is to address a gap in applying proteomics data analysis to forensic applications. MARLOWE produces a list of potential source organisms given confident peptide tags derived from de novo peptide sequencing and a statistical approach to assign peptides to organisms in a probabilistic manner, based on a broad sequence database. Except for the constraints of this underlying broad sequence database, the algorithm assumes no a priori knowledge of potential sources, and the probabilistic way peptides are taxonomically assigned and then scored enables results to be unbiased (within the constraints of the sequence database). In a proof-of-concept study, we examined MARLOWE's performance on two datasets, the Biodiversity dataset and the Bacillus cereus superspecies dataset. Not only did MARLOWE demonstrate successful characterization to true contributors in single source and binary mixtures in the Biodiversity dataset, but also provided sufficient specificity to distinguish species within a bacterial superspecies group. We also compared MARLOWE's results to those of MiCId, a leading microbial identification/characterization tool based on proteomics database search. Comparison of the two tools using 225 mass spectrometry data files yielded comparable performance, with slightly higher accuracy and specificity for MiCId. At the species level, MARLOWE achieved a specificity of 91.4% at 5% FDR. These results suggest that MARLOWE is suitable for candidate- or lead-generation identification of single-organism and binary samples that can generate forensic leads and aid in selecting appropriate follow-on analyses in a forensic context.

Indexed as

Computational BiologyForensic SciencesPeptidesProteomicsSoftwareAlgorithmsBacillus cereusBiodiversityPeptidesDe novo sequence tagsForensic proteomicsMass spectrometryMetaproteomicsStrong peptides

Identifiers

PMID42624859
PMCPMC13494011

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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.