ArticleBMC bioinformatics2015
Probabilistic topic modeling for the analysis and classification of genomic sequences.
Article in BMC bioinformatics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.
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Who cites it
11 citing papers in PubMed.
- Estimating Genome-Wide Phylogenies Using Probabilistic Topic Modeling.Systematic biology · 2025Article
- What Do We Gain When Tolerating Loss? The Information Bottleneck Wrings Out Recombination.Molecular biology and evolution · 2025Article
- A Markov chain-based feature extraction method for classification and identification of cancerous DNA sequences.BioImpacts : BI · 2021Article
- Latent Dirichlet allocation model for world trade analysis.PloS one · 2021Article
- Convolutional neural networks improve fungal classification.Scientific reports · 2020Article
- Whole-GenomeGenes · 2020Article
- A Multi-Label Supervised Topic Model Conditioned on Arbitrary Features for Gene Function Prediction.Genes · 2019Article
- Article
- Superstatistical model of bacterial DNA architecture.Scientific reports · 2017Article
- Understanding Genotype-Phenotype Effects in Cancer via Network Approaches.PLoS computational biology · 2016Review
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4 authors.
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Abstract
backgroundStudies on genomic sequences for classification and taxonomic identification have a leading role in the biomedical field and in the analysis of biodiversity. These studies are focusing on the so-called barcode genes, representing a well defined region of the whole genome. Recently, alignment-free techniques are gaining more importance because they are able to overcome the drawbacks of sequence alignment techniques. In this paper a new alignment-free method for DNA sequences clustering and classification is proposed. The method is based on k-mers representation and text mining techniques.
methodsThe presented method is based on Probabilistic Topic Modeling, a statistical technique originally proposed for text documents. Probabilistic topic models are able to find in a document corpus the topics (recurrent themes) characterizing classes of documents. This technique, applied on DNA sequences representing the documents, exploits the frequency of fixed-length k-mers and builds a generative model for a training group of sequences. This generative model, obtained through the Latent Dirichlet Allocation (LDA) algorithm, is then used to classify a large set of genomic sequences. RESULTS AND
conclusionsWe performed classification of over 7000 16S DNA barcode sequences taken from Ribosomal Database Project (RDP) repository, training probabilistic topic models. The proposed method is compared to the RDP tool and Support Vector Machine (SVM) classification algorithm in a extensive set of trials using both complete sequences and short sequence snippets (from 400 bp to 25 bp). Our method reaches very similar results to RDP classifier and SVM for complete sequences. The most interesting results are obtained when short sequence snippets are considered. In these conditions the proposed method outperforms RDP and SVM with ultra short sequences and it exhibits a smooth decrease of performance, at every taxonomic level, when the sequence length is decreased.
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