Evidence map›Paper›PMID 35783287›Full record

ArticleFrontiers in genetics2022

Gm-PLoc: A Subcellular Localization Model of Multi-Label Protein Based on GAN and DeepFM.

Liwen Wu, Song Gao, Shaowen Yao, Feng Wu, Jie Li, Yunyun Dong, Yunqi Zhang

Abstract read
In one paragraph

Article in Frontiers in genetics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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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3 · Its place in the literature

Who cites it

2 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

7 authors.

Liwen WuEngineering Research Center of Cyberspace, Yunnan University, Kunming, China.
Song GaoEngineering Research Center of Cyberspace, Yunnan University, Kunming, China.
Shaowen YaoEngineering Research Center of Cyberspace, Yunnan University, Kunming, China.
Feng WuEngineering Research Center of Cyberspace, Yunnan University, Kunming, China.
Jie LiEngineering Research Center of Cyberspace, Yunnan University, Kunming, China.
Yunyun DongEngineering Research Center of Cyberspace, Yunnan University, Kunming, China.
Yunqi ZhangEngineering Research Center of Cyberspace, Yunnan University, Kunming, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Identifying the subcellular localization of a given protein is an essential part of biological and medical research, since the protein must be localized in the correct organelle to ensure physiological function. Conventional biological experiments for protein subcellular localization have some limitations, such as high cost and low efficiency, thus massive computational methods are proposed to solve these problems. However, some of these methods need to be improved further for protein subcellular localization with class imbalance problem. We propose a new model, generating minority samples for protein subcellular localization (Gm-PLoc), to predict the subcellular localization of multi-label proteins. This model includes three steps: using the position specific scoring matrix to extract distinguishable features of proteins; synthesizing samples of the minority category to balance the distribution of categories based on the revised generative adversarial networks; training a classifier with the rebalanced dataset to predict the subcellular localization of multi-label proteins. One benchmark dataset is selected to evaluate the performance of the presented model, and the experimental results demonstrate that Gm-PLoc performs well for the multi-label protein subcellular localization.

Indexed as

class imbalance learningdeep learninggenerative adversarial networksmulti-label classificationprotein subcellular localization

Identifiers

PMID35783287
PMCPMC9240597

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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.