Evidence map›Paper›PMID 31725778›Full record

ArticlePloS one2019

An improved deep learning method for predicting DNA-binding proteins based on contextual features in amino acid sequences.

Siquan Hu, Ruixiong Ma, Haiou Wang

Abstract read
In one paragraph

Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
–field-weighted citation impact
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

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3 · Its place in the literature

Who cites it

19 citing papers in PubMed.

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  16. Deep Learning for SARS COV-2 Genome Sequences.IEEE access : practical innovations, open solutions · 2021
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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

3 authors.

Siquan HuSchool of Computer and Communication Engineering, University of Science and Technology Beijing, Beijing, China.
Ruixiong MaSchool of Computer and Communication Engineering, University of Science and Technology Beijing, Beijing, China.ORCID 0000-0002-1604-840X
Haiou WangSchool of Chemistry and Biological Engineering, University of Science and Technology Beijing, Beijing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As the number of known proteins has expanded, how to accurately identify DNA binding proteins has become a significant biological challenge. At present, various computational methods have been proposed to recognize DNA-binding proteins from only amino acid sequences, such as SVM, DNABP and CNN-RNN. However, these methods do not consider the context in amino acid sequences, which makes it difficult for them to adequately capture sequence features. In this study, a new method that coordinates a bidirectional long-term memory recurrent neural network and a convolutional neural network, called CNN-BiLSTM, is proposed to identify DNA binding proteins. The CNN-BiLSTM model can explore the potential contextual relationships of amino acid sequences and obtain more features than can traditional models. The experimental results show that the CNN-BiLSTM achieves a validation set prediction accuracy of 96.5%-7.8% higher than that of SVM, 9.6% higher than that of DNABP and 3.7% higher than that of CNN-RNN. After testing on 20,000 independent samples provided by UniProt that were not involved in model training, the accuracy of CNN-BiLSTM reached 94.5%-12% higher than that of SVM, 4.9% higher than that of DNABP and 4% higher than that of CNN-RNN. We visualized and compared the model training process of CNN-BiLSTM with that of CNN-RNN and found that the former is capable of better generalization from the training dataset, showing that CNN-BiLSTM has a wider range of adaptations to protein sequences. On the test set, CNN-BiLSTM has better credibility because its predicted scores are closer to the sample labels than are those of CNN-RNN. Therefore, the proposed CNN-BiLSTM is a more powerful method for identifying DNA-binding proteins.

Indexed as

Deep LearningAlgorithmsAmino Acid SequenceDNA-Binding ProteinsMemory, Long-TermNeural Networks, ComputerReproducibility of ResultsDNA-Binding Proteins

Identifiers

PMID31725778
PMCPMC6855455

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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.