Evidence map›Paper›PMID 31552241›Full record

ArticleFrontiers in bioengineering and biotechnology2019

A Random Forest Sub-Golgi Protein Classifier Optimized via Dipeptide and Amino Acid Composition Features.

Zhibin Lv, Shunshan Jin, Hui Ding, Quan Zou

Abstract read
In one paragraph

Article in Frontiers in bioengineering and biotechnology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing 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

The trial behind it

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3 · Its place in the literature

Who cites it

45 citing papers in PubMed.

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  8. Identify Bitter Peptides by Using Deep Representation Learning Features.International journal of molecular sciences · 2022
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  16. Prediction of Metal Ion Binding Sites of Transmembrane Proteins.Computational and mathematical methods in medicine · 2021
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  20. Identification of cyclin protein using gradient boost decision tree algorithm.Computational and structural biotechnology journal · 2021
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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

4 authors.

Zhibin LvInstitute of Fundamental and Frontier Sciences, University of Electronic Science and Technology of China, Chengdu, China.
Shunshan JinDepartment of Neurology, Heilongjiang Province Land Reclamation Headquarters General Hospital, Harbin, China.
Hui DingCenter for Informational Biology, University of Electronic Science and Technology of China, Chengdu, China.
Quan ZouInstitute of Fundamental and Frontier Sciences, University of Electronic Science and Technology of China, Chengdu, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To gain insight into the malfunction of the Golgi apparatus and its relationship to various genetic and neurodegenerative diseases, the identification of sub-Golgi proteins, both cis-Golgi and trans-Golgi proteins, is of great significance. In this study, a state-of-art random forests sub-Golgi protein classifier, rfGPT, was developed. The rfGPT used 2-gap dipeptide and split amino acid composition for the feature vectors and was combined with the synthetic minority over-sampling technique (SMOTE) and an analysis of variance (ANOVA) feature selection method. The rfGPT was trained on a sub-Golgi protein sequence data set (137 sequences), with sequence identity less than 25%. For the optimal rfGPT classifier with 93 features, the accuracy (ACC) was 90.5%; the Matthews correlation coefficient (MCC) was 0.811; the sensitivity (Sn) was 92.6%; and the specificity (Sp) was 88.4%. The independent testing scores for the rfGPT were ACC = 90.6%; MCC = 0.696; Sn = 96.1%; and Sp = 69.2%. Although the independent testing accuracy was 4.4% lower than that for the best reported sub-Golgi classifier trained on a data set with 40% sequence identity (304 sequences), the rfGPT is currently the top sub-Golgi protein predictor utilizing feature vectors without any position-specific scoring matrix and its derivative features. Therefore, the rfGPT is a more practical tool, because no sequence alignment is required with tens of millions of protein sequences. To date, the rfGPT is the Golgi classifier with the best independent testing scores, optimized by training on smaller benchmark data sets. Feature importance analysis proves that the non-polar and aliphatic residues composition, the (aromatic residues) + (non-polar, aliphatic residues) dipeptide and aromatic residues composition between NH2-termial and COOH-terminal of protein sequences are the three top biological features for distinguishing the sub-Golgi proteins.

Indexed as

ANOVA feature selectionk-gap dipeptiderandom forestssplit amino acid compositionsub-Golgi protein classifiersynthetic minority over-sampling

Identifiers

PMID31552241
PMCPMC6737778

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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.