Evidence map›Paper›PMID 42898793›Full record

ArticleNAR genomics and bioinformatics2026

DNA augmentations for semi-supervised learning in genomic sequence classification.

Hyunwoo Yoo, Gail L Rosen

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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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

2 authors.

Hyunwoo YooDepartment of Electrical and Computer Engineering, Drexel University, 3141 Chestnut St, Philadelphia, PA 19104, United States.ORCID https://orcid.org/0000-0003-3862-4006
Gail L RosenDepartment of Electrical and Computer Engineering, Drexel University, 3141 Chestnut St, Philadelphia, PA 19104, United States.ORCID https://orcid.org/0000-0003-1763-5750

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Semi-supervised learning (SSL) is a natural fit for genomics, where unlabeled sequences are abundant but high-quality labels are scarce due to costly curation. However, most SSL pipelines rely on generic perturbations that are not tailored to biological constraints, and it remains unclear which augmentation designs yield reliable gains for DNA sequence classification. In this application note, we present an empirical study of genome-aware weak-strong augmentation recipes for pseudo-label-based SSL, focusing on FixMatch and FlexMatch with a GROVER DNA language model backbone. Across two classification benchmarks-antimicrobial resistance (AMR) drug-class prediction from AMR gene sequences and multi-class oncovirus family classification from simulated 150 bp tumor-like reads-we systematically evaluate 25 weak/strong augmentation pairs constructed from biologically motivated operators, including reverse-complement, codon-level back-translation, mild masking/substitution (NN), high-rate substitution, and length-preserving insertion-deletion (indel). We find consistent trends: (i) moderate, sequence-preserving perturbations yield the best accuracy-stability trade-off, (ii) excessive masking or aggressive mutation increases variance and degrades performance, and (iii) short-segment masking (NN) for weak augmentation followed by an indel rate (around 5%) for strong augmentation emerge as a robust strategy to learn from unlabeled genomic data. We release implementations and recommended defaults to facilitate reproducible SSL for genomic sequence modeling under limited-label regimes.

Indexed as

DNAGenomicsSequence Analysis, DNASupervised Machine LearningAlgorithmsHumansDNA

Identifiers

PMID42898793
PMCPMC13678202

What OpenQuestion holds

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Registered trials

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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.