Evidence map›Paper›PMID 40563247›Full record

ArticleBioinformatics (Oxford, England)2025

SetBERT: the deep learning platform for contextualized embeddings and explainable predictions from high-throughput sequencing.

David W Ludwig, Christopher Guptil, Nicholas R Alexander, Kateryna Zhalnina, Edi M-L Wipf, Albina Khasanova, Nicholas A Barber, Wesley Swingley, Donald M Walker, Joshua L Phillips

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
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

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

2 citing papers in PubMed.

  1. Article
  2. Article
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

10 authors.

David W LudwigDepartment of Computer Science, Middle Tennessee State University, Murfreesboro, TN 37132, United States.ORCID 0009-0001-5851-7964
Christopher GuptilDepartment of Mathematics and Computer Science, Miami University, Oxford, OH 45056, United States.
Nicholas R AlexanderDepartment of Biology, Middle Tennessee State University, Murfreesboro, TN 37132, United States.ORCID 0009-0004-7271-5520
Kateryna ZhalninaEnvironmental Genomics and Systems Biology, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, United States.ORCID 0000-0002-1893-1888
Edi M-L WipfEnvironmental Genomics and Systems Biology, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, United States.ORCID 0000-0002-1025-9310
Albina KhasanovaEnvironmental Genomics and Systems Biology, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, United States.ORCID 0000-0001-6652-012X
Nicholas A BarberDepartment of Biology, San Diego State University, San Diego, CA 92182, United States.ORCID 0000-0003-1653-0009
Wesley SwingleyDepartment of Biological Sciences, Northern Illinois University, DeKalb, IL 60115, United States.ORCID 0000-0001-7734-5179
Donald M WalkerDepartment of Biology, Middle Tennessee State University, Murfreesboro, TN 37132, United States.ORCID 0000-0003-3119-8809
Joshua L PhillipsDepartment of Computer Science, Middle Tennessee State University, Murfreesboro, TN 37132, United States.ORCID 0000-0002-4619-6083

Funding

National Science FoundationNational Science Foundation #1933925National Science Foundation #1937232National Science Foundation #1937255
6 · The paper itself

Abstract

motivationHigh-throughput sequencing (HTS) is a modern sequencing technology used to profile microbiomes by sequencing thousands of short genomic fragments from the microorganisms within a given sample. This technology presents a unique opportunity for artificial intelligence to comprehend the underlying functional relationships of microbial communities. However, due to the unstructured nature of HTS data, nearly all computational models are limited to processing DNA sequences individually. This limitation causes them to miss out on key interactions between microorganisms, significantly hindering our understanding of how these interactions influence the microbial communities as a whole. Furthermore, most computational methods rely on post-processing of samples which could inadvertently introduce unintentional protocol-specific bias.

resultsAddressing these concerns, we present SetBERT, a robust pre-training methodology for creating generalized deep learning models for processing HTS data to produce contextualized embeddings and be fine-tuned for downstream tasks with explainable predictions. By leveraging sequence interactions, we show that SetBERT significantly outperforms other models in taxonomic classification with genus-level classification accuracy of 95%. Furthermore, we demonstrate that SetBERT is able to accurately explain its predictions autonomously by confirming the biological-relevance of taxa identified by the model. AVAILABILITY AND IMPLEMENTATION: All source code is available at https://github.com/DLii-Research/setbert. SetBERT may be used through the q2-deepdna QIIME 2 plugin whose source code is available at https://github.com/DLii-Research/q2-deepdna.

Indexed as

Deep LearningHigh-Throughput Nucleotide SequencingMicrobiotaSequence Analysis, DNASoftwareAlgorithmsComputational Biology

Identifiers

PMID40563247
PMCPMC12245400

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.