ArticleBioinformatics (Oxford, England)2013
Poly(A) motif prediction using spectral latent features from human DNA sequences.
Article in Bioinformatics (Oxford, England), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.
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Who cites it
20 citing papers in PubMed.
- PolyA-GLM: A comprehensive framework forComputational and structural biotechnology journal · 2026Article
- Known sequence features explain half of all human gene ends.NAR genomics and bioinformatics · 2023Article
- Accurate transcriptome-wide identification and quantification of alternative polyadenylation from RNA-seq data with APAIQ.Genome research · 2023Article
- A Survey on Methods for Predicting Polyadenylation Sites from DNA Sequences, Bulk RNA-seq, and Single-cell RNA-seq.Genomics, proteomics & bioinformatics · 2023Review
- Motif and conserved module analysis in DNA (promoters, enhancers) and RNA (lncRNA, mRNA) using AlModules.Scientific reports · 2022Article
- DeeReCT-APA: Prediction of Alternative Polyadenylation Site Usage Through Deep Learning.Genomics, proteomics & bioinformatics · 2022Article
- From shallow to deep: some lessons learned from application of machine learning for recognition of functional genomic elements in human genome.Human genomics · 2022Review
- Splice2Deep: An ensemble of deep convolutional neural networks for improved splice site prediction in genomic DNA.Gene: X · 2020Article
- Poly(A)-DG: A deep-learning-based domain generalization method to identify cross-species Poly(A) signal without prior knowledge from target species.PLoS computational biology · 2020Article
- C-RNNCrispr: Prediction of CRISPR/Cas9 sgRNA activity using convolutional and recurrent neural networks.Computational and structural biotechnology journal · 2020Article
- DeeReCT-PolyA: a robust and generic deep learning method for PAS identification.Bioinformatics (Oxford, England) · 2019Article
- DeepGSR: an optimized deep-learning structure for the recognition of genomic signals and regions.Bioinformatics (Oxford, England) · 2019Article
- A Novel Hybrid CNN-SVR for CRISPR/Cas9 Guide RNA Activity Prediction.Frontiers in genetics · 2019Article
- Inference of the human polyadenylation code.Bioinformatics (Oxford, England) · 2018Article
- Omni-PolyA: a method and tool for accurate recognition of Poly(A) signals in human genomic DNA.BMC genomics · 2017Article
- Poly(A) code analyses reveal key determinants for tissue-specific mRNA alternative polyadenylation.RNA (New York, N.Y.) · 2016Article
- Spectacle: fast chromatin state annotation using spectral learning.Genome biology · 2015Article
- Modeling DNA affinity landscape through two-round support vector regression with weighted degree kernels.BMC systems biology · 2014Article
- Article
- The Advances in Deep Learning Modeling of Polyadenylation Codes.Wiley interdisciplinary reviews. RNAReview
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5 authors.
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No grant is acknowledged in the PubMed record.
Abstract
motivationPolyadenylation is the addition of a poly(A) tail to an RNA molecule. Identifying DNA sequence motifs that signal the addition of poly(A) tails is essential to improved genome annotation and better understanding of the regulatory mechanisms and stability of mRNA. Existing poly(A) motif predictors demonstrate that information extracted from the surrounding nucleotide sequences of candidate poly(A) motifs can differentiate true motifs from the false ones to a great extent. A variety of sophisticated features has been explored, including sequential, structural, statistical, thermodynamic and evolutionary properties. However, most of these methods involve extensive manual feature engineering, which can be time-consuming and can require in-depth domain knowledge.
resultsWe propose a novel machine-learning method for poly(A) motif prediction by marrying generative learning (hidden Markov models) and discriminative learning (support vector machines). Generative learning provides a rich palette on which the uncertainty and diversity of sequence information can be handled, while discriminative learning allows the performance of the classification task to be directly optimized. Here, we used hidden Markov models for fitting the DNA sequence dynamics, and developed an efficient spectral algorithm for extracting latent variable information from these models. These spectral latent features were then fed into support vector machines to fine-tune the classification performance. We evaluated our proposed method on a comprehensive human poly(A) dataset that consists of 14 740 samples from 12 of the most abundant variants of human poly(A) motifs. Compared with one of the previous state-of-the-art methods in the literature (the random forest model with expert-crafted features), our method reduces the average error rate, false-negative rate and false-positive rate by 26, 15 and 35%, respectively. Meanwhile, our method makes ~30% fewer error predictions relative to the other string kernels. Furthermore, our method can be used to visualize the importance of oligomers and positions in predicting poly(A) motifs, from which we can observe a number of characteristics in the surrounding regions of true and false motifs that have not been reported before. AVAILABILITY: http://sfb.kaust.edu.sa/Pages/Software.aspx. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
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