ArticleScientific reports2025
Innovative data augmentation strategy for deep learning on biological datasets with limited gene representations focused on chloroplast genomes.
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.
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.
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.
Who cites it
3 citing papers in PubMed.
- Balanced DNA interpolation improves learning of genetic distance-informed embeddings in plants.PLoS computational biology · 2026Article
- Using transfer learning approaches to predict RNA-Seq gene expression data for cancer classification.Frontiers in artificial intelligence · 2026Article
- Deep learning-based investigation of chloroplast translation regulatory sequences.Frontiers in plant science · 2025Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
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
Identifiers
What OpenQuestion holds
Registered trials
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.