Evidence map›Paper›PMID 42713011›Full record

ArticleNAR genomics and bioinformatics2026

LAMBDA: a prophage detection benchmark for genomic language models.

LeAnn M Lindsey, Nicole L Pershing, Keith Dufault-Thompson, Ho-Jin Gwak, Anisa Habib, Aaron Schindler, Arjun Rakheja, June L Round, W Zac Stephens, Anne J Blaschke and 2 more

Abstract read
In one paragraph

Article in NAR genomics and bioinformatics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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

5 · Who and what money

Authors and funding

12 authors.

LeAnn M LindseyNational Library of Medicine, National Institutes of Health, Bethesda, MD, 20892, United States.
Nicole L PershingDepartment of Pediatrics, School of Medicine, University of Utah, Salt Lake City, UT, 84132, United States.ORCID https://orcid.org/0000-0002-5399-5668
Keith Dufault-ThompsonNational Library of Medicine, National Institutes of Health, Bethesda, MD, 20892, United States.ORCID https://orcid.org/0000-0002-0991-2255
Ho-Jin GwakNational Library of Medicine, National Institutes of Health, Bethesda, MD, 20892, United States.ORCID https://orcid.org/0000-0001-7765-0827
Anisa HabibDepartment of Computer Science, Kahlert School of Computing, University of Utah, Salt Lake City, UT, 84112, United States.
Aaron SchindlerDepartment of Computer Science, Kahlert School of Computing, University of Utah, Salt Lake City, UT, 84112, United States.
Arjun RakhejaNational Library of Medicine, National Institutes of Health, Bethesda, MD, 20892, United States.
June L RoundDepartment of Pathology, School of Medicine, University of Utah, Salt Lake City, UT, 84132, United States.
W Zac StephensDepartment of Pathology, School of Medicine, University of Utah, Salt Lake City, UT, 84132, United States.ORCID https://orcid.org/0000-0002-8072-9023
Anne J BlaschkeDepartment of Pediatrics, School of Medicine, University of Utah, Salt Lake City, UT, 84132, United States.
Hari SundarDepartment of Computer Science, Tufts University, Medford, MA, 02155, United States.
Xiaofang JiangNational Library of Medicine, National Institutes of Health, Bethesda, MD, 20892, United States.ORCID https://orcid.org/0000-0002-0955-8284

Funding

Antibody targeting of the viromeU01AT012990 · NCCIH · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI June Louise Round, Zac Stephens · 2024 to 2026
$5.2M
CTSA K12 Program at University of Utah: Early Career Faculty Development ProgramK12TR004413 · NCATS · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI MAUREEN A MURTAUGH, Corrine Ione Voils · 2023 to 2026
$3.9M
NCATS NIH HHS K12 TR004413NCCIH NIH HHS U01 AT012990
6 · The paper itself

Abstract

Transformer-based genomic sequence models represent an emerging frontier in computational biology. Yet, their embeddings have not yet shown the same level of predictive power as natural and protein language models, highlighting a gap between current implementations and theoretical promise. Existing benchmarks for DNA language models primarily focus on classifying regulatory elements in eukaryotic genomes, leaving open the fundamental question of whether these models learn sequence-level features across whole genomes. We introduce LAMBDA, a benchmark designed to rigorously evaluate genome language model embeddings through phage-bacteria sequence discrimination across four categories of increasing complexity: probing tasks, fine-tuning assessments, diagnostic tests, and genome-wide prophage detection. Our comprehensive analysis of current genomic language models provides insight into the importance of training data selection relative to model size, the need for domain-specific training, and the capabilities and limitations of genomic language models for detecting prophage sequences. This benchmark represents a challenging genomic annotation task in the bacterial domain and addresses a key computational problem with direct relevance to microbiology and medicine.

Indexed as

Bacteriophage lambdaGenomicsModels, GeneticProphagesBenchmarkingComputational BiologyGenome, BacterialLarge Language Models

Identifiers

PMID42713011
PMCPMC13551034

What OpenQuestion holds

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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.