Evidence map›Paper›PMID 33914130›Full record

ArticleMolecular genetics and genomics : MGG2021

Predicting gene phenotype by multi-label multi-class model based on essential functional features.

Lei Chen, Zhandong Li, Tao Zeng, Yu-Hang Zhang, Hao Li, Tao Huang, Yu-Dong Cai

Abstract read
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In one paragraph

Article in Molecular genetics and genomics : MGG, 2021. 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

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

7 citing papers in PubMed.

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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

7 authors.

Lei Chen *School of Life Sciences, Shanghai University, Shanghai, 200444, People's Republic of China.
Zhandong Li *College of Food Engineering, Jilin Engineering Normal University, Changchun, 130052, People's Republic of China.
Tao ZengCAS Key Laboratory of Computational Biology, Bio-Med Big Data Center, Shanghai Institute of Nutrition and Health, University of Chinese Academy of Sciences, Chinese Academy of Sciences, Shanghai, 200031, People's Republic of China.
Yu-Hang ZhangChanning Division of Network Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Hao LiCollege of Food Engineering, Jilin Engineering Normal University, Changchun, 130052, People's Republic of China.
Tao HuangKey Laboratory of Tissue Microenvironment and Tumor, Shanghai Institute of Nutrition and Health, Chinese Academy of Sciences, Shanghai, 200031, People's Republic of China. tohuangtao@126.com.
Yu-Dong CaiSchool of Life Sciences, Shanghai University, Shanghai, 200444, People's Republic of China. cai_yud@126.com.ORCID http://orcid.org/0000-0001-5664-7979

Funding

Fund of the Key Laboratory of Tissue Microenvironment and Tumor of Chinese Academy of Sciences 202002National Key R&D Program of China 2017YFC1201200National Key R&D Program of China 2018YFC0910403National Natural Science Foundation of China 31701151Shanghai Municipal Science and Technology Major Project 2017SHZDZX01Shanghai Sailing Program 16YF1413800Strategic Priority Research Program of Chinese Academy of Sciences XDB38050200Youth Innovation Promotion Association of the Chinese Academy of Sciences 2016245
6 · The paper itself

Abstract

Phenotype is one of the most significant concepts in genetics, which is used to describe all the characteristics of a research object that can be observed. Considering that phenotype reflects the integrated features of genotype and environment factors, it is hard to define phenotype characteristics, even difficult to predict unknown phenotypes. Restricted by current biological techniques, it is still quite expensive and time-consuming to obtain sufficient structural information of large-scale phenotype-associated genes/proteins. Various bioinformatics methods have been presented to solve such problem, and researchers have confirmed the efficacy and prediction accuracy of functional network-based prediction. But general functional descriptions have highly complicated inner structures for phenotype prediction. To further address this issue and improve the efficacy of phenotype prediction on more than ten kinds of phenotypes, we first extract functional enrichment features from GO and KEGG, and then use node2vec to learn functional embedding features of genes from a gene-gene network. All these features are analyzed by some feature selection methods (Boruta, minimum redundancy maximum relevance) to generate a feature list. Such list is fed into the incremental feature selection, incorporating some multi-label classifiers built by RAkEL and some classic base classifiers, to build an optimum multi-label multi-class classification model for phenotype prediction. According to recent researches, our method has indeed identified many literature-supported genes/proteins and their associated phenotypes, and even some candidate genes with re-assigned new phenotypes, which provide a new computational tool for the accurate and effective phenotypic prediction.

Indexed as

AlgorithmsComputational BiologyDatasets as TopicGene Regulatory NetworksGenetic Association StudiesMetabolic Networks and PathwaysPhenotypeProteinsSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsStructure-Activity RelationshipProteinsSaccharomyces cerevisiae ProteinsFeature selectionFunctional enrichmentMulti-label classificationNetwork embeddingPhenotypeRAkEL

Identifiers

What Socratic holds

Textmetadata
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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 Socratic graph.