Evidence map›Paper›PMID 31245182›Full record

ArticlePeerJ2019

An integration of deep learning with feature embedding for protein-protein interaction prediction.

Yu Yao, Xiuquan Du, Yanyu Diao, Huaixu Zhu

Abstract read
In one paragraph

Article in PeerJ, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing 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

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

49 citing papers in PubMed.

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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

4 authors.

Yu Yao *The School of Computer Science and Technology, Anhui University, Hefei, Anhui, China.
Xiuquan Du *The School of Computer Science and Technology, Anhui University, Hefei, Anhui, China.
Yanyu DiaoThe School of Computer Science and Technology, Anhui University, Hefei, Anhui, China.
Huaixu ZhuThe School of Computer Science and Technology, Anhui University, Hefei, Anhui, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Protein-protein interactions are closely relevant to protein function and drug discovery. Hence, accurately identifying protein-protein interactions will help us to understand the underlying molecular mechanisms and significantly facilitate the drug discovery. However, the majority of existing computational methods for protein-protein interactions prediction are focused on the feature extraction and combination of features and there have been limited gains from the state-of-the-art models. In this work, a new residue representation method named Res2vec is designed for protein sequence representation. Residue representations obtained by Res2vec describe more precisely residue-residue interactions from raw sequence and supply more effective inputs for the downstream deep learning model. Combining effective feature embedding with powerful deep learning techniques, our method provides a general computational pipeline to infer protein-protein interactions, even when protein structure knowledge is entirely unknown. The proposed method DeepFE-PPI is evaluated on the S. Cerevisiae and human datasets. The experimental results show that DeepFE-PPI achieves 94.78% (accuracy), 92.99% (recall), 96.45% (precision), 89.62% (Matthew's correlation coefficient, MCC) and 98.71% (accuracy), 98.54% (recall), 98.77% (precision), 97.43% (MCC), respectively. In addition, we also evaluate the performance of DeepFE-PPI on five independent species datasets and all the results are superior to the existing methods. The comparisons show that DeepFE-PPI is capable of predicting protein-protein interactions by a novel residue representation method and a deep learning classification framework in an acceptable level of accuracy. The codes along with instructions to reproduce this work are available from https://github.com/xal2019/DeepFE-PPI.

Indexed as

Deep learningFeature embeddingMachine learningprotein–protein interaction

Identifiers

PMID31245182
PMCPMC6585896

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.