Evidence map›Paper›PMID 39913380›Full record

ArticleBioinformatics (Oxford, England)2025

Embed-Search-Align: DNA sequence alignment using Transformer models.

Pavan Holur, K C Enevoldsen, Shreyas Rajesh, Lajoyce Mboning, Thalia Georgiou, Louis-S Bouchard, Matteo Pellegrini, Vwani Roychowdhury

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 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
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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

8 authors.

Pavan HolurDepartment of Electrical and Computer Engineering, UCLA, Los Angeles, California, 90024, United States.ORCID 0000-0002-8495-9416
K C EnevoldsenCenter for Humanities Computing, Aarhus University, Aarhus, 8000, Denmark.
Shreyas RajeshDepartment of Electrical and Computer Engineering, UCLA, Los Angeles, California, 90024, United States.
Lajoyce MboningDepartment of Chemistry and Biochemistry, UCLA, Los Angeles, California, 90024, United States.
Thalia GeorgiouDepartment of Biochemistry, Biophysics, and Structural Biology (MBIDP), UCLA, Los Angeles, California, 90024, United States.
Louis-S BouchardDepartment of Chemistry and Biochemistry, UCLA, Los Angeles, California, 90024, United States.
Matteo PellegriniDepartment of Molecular, Cell, and Developmental Biology, UCLA, Los Angeles, California, 90024, United States.
Vwani RoychowdhuryDepartment of Electrical and Computer Engineering, UCLA, Los Angeles, California, 90024, United States.

Funding

Training Grant in Genomic Analysis and InterpretationT32HG002536 · NHGRI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Valerie A Arboleda, Harold Pimentel · 2002 to 2026
$8.6M
NHGRI NIH HHS T32 HG002536
6 · The paper itself

Abstract

motivationDNA sequence alignment, an important genomic task, involves assigning short DNA reads to the most probable locations on an extensive reference genome. Conventional methods tackle this challenge in two steps: genome indexing followed by efficient search to locate likely positions for given reads. Building on the success of Large Language Models in encoding text into embeddings, where the distance metric captures semantic similarity, recent efforts have encoded DNA sequences into vectors using Transformers and have shown promising results in tasks involving classification of short DNA sequences. Performance at sequence classification tasks does not, however, guarantee sequence alignment, where it is necessary to conduct a genome-wide search to align every read successfully, a significantly longer-range task by comparison.

resultsWe bridge this gap by developing a "Embed-Search-Align" (ESA) framework, where a novel Reference-Free DNA Embedding (RDE) Transformer model generates vector embeddings of reads and fragments of the reference in a shared vector space; read-fragment distance metric is then used as a surrogate for sequence similarity. ESA introduces: (i) Contrastive loss for self-supervised training of DNA sequence representations, facilitating rich reference-free, sequence-level embeddings, and (ii) a DNA vector store to enable search across fragments on a global scale. RDE is 99% accurate when aligning 250-length reads onto a human reference genome of 3 gigabases (single-haploid), rivaling conventional algorithmic sequence alignment methods such as Bowtie and BWA-Mem. RDE far exceeds the performance of six recent DNA-Transformer model baselines such as Nucleotide Transformer, Hyena-DNA, and shows task transfer across chromosomes and species. AVAILABILITY AND IMPLEMENTATION: Please see https://anonymous.4open.science/r/dna2vec-7E4E/readme.md.

Indexed as

Sequence AlignmentSequence Analysis, DNAAlgorithmsBase SequenceDNAGenomicsHumansSoftwareDNA

Identifiers

PMID39913380
PMCPMC11919449

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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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.