Evidence map›Paper›PMID 32655275›Full record

ArticleEvolutionary bioinformatics online2020

Using Random Forest Model Combined With Gabor Feature to Predict Protein-Protein Interaction From Protein Sequence.

Xin-Ke Zhan, Zhu-Hong You, Li-Ping Li, Yang Li, Zheng Wang, Jie Pan

Abstract read
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Article in Evolutionary bioinformatics online, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

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3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

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4 · The record

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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

6 authors.

Xin-Ke ZhanSchool of Information Engineering, Xijing University, Xi'an, China.
Zhu-Hong YouSchool of Information Engineering, Xijing University, Xi'an, China.
Li-Ping LiSchool of Information Engineering, Xijing University, Xi'an, China.
Yang LiSchool of Information Engineering, Xijing University, Xi'an, China.
Zheng WangSchool of Information Engineering, Xijing University, Xi'an, China.
Jie PanSchool of Information Engineering, Xijing University, Xi'an, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Protein-protein interactions (PPIs) play a crucial role in the life cycles of living cells. Thus, it is important to understand the underlying mechanisms of PPIs. Although many high-throughput technologies have generated large amounts of PPI data in different organisms, the experiments for detecting PPIs are still costly and time-consuming. Therefore, novel computational methods are urgently needed for predicting PPIs. For this reason, developing a new computational method for predicting PPIs is drawing more and more attention. In this study, we proposed a novel computational method based on texture feature of protein sequence for predicting PPIs. Especially, the Gabor feature is used to extract texture feature and protein evolutionary information from Position-Specific Scoring Matrix, which is generated by Position-Specific Iterated Basic Local Alignment Search Tool. Then, random forest-based classifiers are used to infer the protein interactions. When performed on PPI data sets of

Indexed as

Gabor featuresprotein-protein interactionsProtein sequencerandom forest

Identifiers

PMID32655275
PMCPMC7328357

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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.