Evidence map›Paper›PMID 31510705›Full record

ArticleBioinformatics (Oxford, England)2019

Multifaceted protein-protein interaction prediction based on Siamese residual RCNN.

Muhao Chen, Chelsea J-T Ju, Guangyu Zhou, Xuelu Chen, Tianran Zhang, Kai-Wei Chang, Carlo Zaniolo, Wei Wang

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 152 papers.

0numbers the graph read from it
0cells of the map it votes in
152citing 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

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.

3 · Its place in the literature

Who cites it

152 citing papers in PubMed.

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  16. Rapid Proteome-Wide Discovery of Protein-Protein Interactions With ppIRIS.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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92 more citing papers are in PubMed but not listed here.

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

8 authors.

Muhao ChenDepartment of Computer Science, University of California, Los Angeles, Los Angeles, CA, USA.
Chelsea J-T JuDepartment of Computer Science, University of California, Los Angeles, Los Angeles, CA, USA.
Guangyu ZhouDepartment of Computer Science, University of California, Los Angeles, Los Angeles, CA, USA.
Xuelu ChenDepartment of Computer Science, University of California, Los Angeles, Los Angeles, CA, USA.
Tianran ZhangDepartment of Bioengineering, University of California, Los Angeles, Los Angeles, CA, USA.
Kai-Wei ChangDepartment of Computer Science, University of California, Los Angeles, Los Angeles, CA, USA.
Carlo ZanioloDepartment of Computer Science, University of California, Los Angeles, Los Angeles, CA, USA.
Wei WangDepartment of Computer Science, University of California, Los Angeles, Los Angeles, CA, USA.

Funding

TRAININGU54GM114833 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI LINDSEY, MERRY L., PING, PEIPEI · 2014 to 2017
$13.8M
Fast and Robust Methods for Large Scale Genotype Phenotype Association StudyR01GM115833 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI WANG, WEI · 2015 to 2017
$933k
NIGMS NIH HHS R01 GM115833NIGMS NIH HHS U54 GM114833
6 · The paper itself

Abstract

motivationSequence-based protein-protein interaction (PPI) prediction represents a fundamental computational biology problem. To address this problem, extensive research efforts have been made to extract predefined features from the sequences. Based on these features, statistical algorithms are learned to classify the PPIs. However, such explicit features are usually costly to extract, and typically have limited coverage on the PPI information.

resultsWe present an end-to-end framework, PIPR (Protein-Protein Interaction Prediction Based on Siamese Residual RCNN), for PPI predictions using only the protein sequences. PIPR incorporates a deep residual recurrent convolutional neural network in the Siamese architecture, which leverages both robust local features and contextualized information, which are significant for capturing the mutual influence of proteins sequences. PIPR relieves the data pre-processing efforts that are required by other systems, and generalizes well to different application scenarios. Experimental evaluations show that PIPR outperforms various state-of-the-art systems on the binary PPI prediction problem. Moreover, it shows a promising performance on more challenging problems of interaction type prediction and binding affinity estimation, where existing approaches fall short. AVAILABILITY AND IMPLEMENTATION: The implementation is available at https://github.com/muhaochen/seq_ppi.git. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.

Indexed as

Computational BiologyNeural Networks, ComputerAlgorithmsAmino Acid SequenceProtein BindingProteinsProteins

Identifiers

PMID31510705
PMCPMC6681469

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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.