Evidence map›Paper›PMID 35286461›Full record

ArticleAmino acids2022

ATGPred-FL: sequence-based prediction of autophagy proteins with feature representation learning.

Shihu Jiao, Zheng Chen, Lichao Zhang, Xun Zhou, Lei Shi

Abstract read
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In one paragraph

Article in Amino acids, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.7field-weighted citation impact, top 34% of its field
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

6 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Autophagy and machine learning: Unanswered questions.Biochimica et biophysica acta. Molecular basis of disease · 2024
    Review
  5. Article
  6. Article
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

5 authors at 4 institutions in 1 country.

Shihu Jiao *Yangtze Delta Region Institute (Quzhou), University of Electronic Science and Technology of China, Quzhou, China.ORCID http://orcid.org/0000-0001-7428-4876
Zheng Chen *School of Applied Chemistry and Biological Technology, Shenzhen Polytechnic, 7098 Liuxian Street, Shenzhen, 518055, China.
Lichao ZhangSchool of Intelligent Manufacturing and Equipment, Shenzhen Institute of Information Technology, Shenzhen, 518172, China.
Xun ZhouBeidahuang Industry Group General Hospital, Harbin, 150001, China. xunzhoucyy@163.com.
Lei ShiDepartment of Spine Surgery, Changzheng Hospital, Naval Medical University, No 415, Fengyang Road, Huangpu District, Shanghai, 210000, China. slspine@163.com.
University of Electronic Science and Technology of China · CNHebei General Hospital · CNShanghai Changzheng Hospital · CNShenzhen Institute of Information Technology · CN

Funding

National Natural Science Foundation of China 62101353National Natural Science Foundation of China No.62002244Special Science Foundation of Quzhou 2020D003
6 · The paper itself

Abstract

Autophagy plays an important role in biological evolution and is regulated by many autophagy proteins. Accurate identification of autophagy proteins is crucially important to reveal their biological functions. Due to the expense and labor cost of experimental methods, it is urgent to develop automated, accurate and reliable sequence-based computational tools to enable the identification of novel autophagy proteins among numerous proteins and peptides. For this purpose, a new predictor named ATGPred-FL was proposed for the efficient identification of autophagy proteins. We investigated various sequence-based feature descriptors and adopted the feature learning method to generate corresponding, more informative probability features. Then, a two-step feature selection strategy based on accuracy was utilized to remove irrelevant and redundant features, leading to the most discriminative 14-dimensional feature set. The final predictor was built using a support vector machine classifier, which performed favorably on both the training and testing sets with accuracy values of 94.40% and 90.50%, respectively. ATGPred-FL is the first ATG machine learning predictor based on protein primary sequences. We envision that ATGPred-FL will be an effective and useful tool for autophagy protein identification, and it is available for free at http://lab.malab.cn/~acy/ATGPred-FL , the source code and datasets are accessible at https://github.com/jiaoshihu/ATGPred .

Indexed as

Computational BiologyProteinsAlgorithmsAutophagyMachine LearningSoftwareSupport Vector MachineProteinsAutophagy proteinComputational predictionFeature representation learning schemeFeature selectionSupport vector machine

Identifiers

PMID35286461
OpenAlexW4220800455

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.