Evidence map›Paper›PMID 40715495›Full record

ArticleScientific reports2025

Innovative data augmentation strategy for deep learning on biological datasets with limited gene representations focused on chloroplast genomes.

Mohammad Ali Abbasi-Vineh, Shirin Rouzbahani, Kaveh Kavousi, Masoumeh Emadpour

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In one paragraph

Article in Scientific reports, 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

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3 · Its place in the literature

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3 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Mohammad Ali Abbasi-VinehDepartment of Agricultural Biotechnology, Tarbiat Modares University (TMU), Tehran, 1497713111, Iran.
Shirin RouzbahaniDepartment of Agricultural Biotechnology, Tarbiat Modares University (TMU), Tehran, 1497713111, Iran.
Kaveh KavousiDepartment of Bioinformatics, Laboratory of Complex Biological Systems and Bioinformatics (CBB), Institute of Biochemistry and Biophysics (IBB), University of Tehran, Tehran, Iran. kkavousi@ut.ac.ir.
Masoumeh EmadpourDepartment of Agricultural Biotechnology, Tarbiat Modares University (TMU), Tehran, 1497713111, Iran. m.emadpour@modares.ac.ir.

Funding

Tarbiat Modares University 86132
6 · The paper itself

Abstract

One key barrier to applying deep learning (DL) to omics and other biological datasets is data scarcity, particularly when each gene or protein is represented by a single sequence. This fundamental challenge is mainly relevant in research involving genetically constrained organisms, organelles, specialized cell types, and biological cycles and pathways. This study introduces a novel data augmentation strategy designed to facilitate the application of DL models to omics datasets. This approach generated a high number of overlapping subsequences with controlled overlaps and shared nucleotide features through a sliding window technique. A hybrid model of Convolutional Neural Network (CNN) and Long Short-Term Memory (LSTM) layers was applied across augmented datasets comprising genes and proteins from eight microalgae and higher plant chloroplasts. The data augmentation strategy enabled employing DL methods on these datasets and significantly improved the model performance by avoiding common issues such as overfitting and non-representative sequence variations. The current augmentation process is highly adaptable, providing flexibility across different types of biological data repositories. Furthermore, a complementary k-mer-based data augmentation strategy was introduced for unlabeled datasets, enhancing unsupervised analysis. Overall, these innovative strategies provide robust solutions for optimizing model training potential in the study of datasets with limited data availability.

Indexed as

ChloroplastsComputational BiologyDeep LearningGenome, ChloroplastDatabases, GeneticMicroalgaeNeural Networks, ComputerChloroplast genomeGenomicsMachine learningProteomicsSmall dataTranscriptomics

Identifiers

PMID40715495
PMCPMC12297658

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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.