Evidence map›Paper›PMID 34646831›Full record

ArticleFrontiers in cell and developmental biology2021

Large Scale Identification of Osteosarcoma Pathogenic Genes by Multiple Extreme Learning Machine.

Zhipeng Zhao, Jijun Shi, Guang Zhao, Yanjun Gao, Zhigang Jiang, Fusheng Yuan

Abstract read
In one paragraph

Article in Frontiers in cell and developmental biology, 2021. 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

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2 · The registry

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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

6 authors.

Zhipeng ZhaoDepartment of Basic Medical Sciences, Taizhou University, Taizhou, China.
Jijun ShiDepartment of Orthopedics, Songyuan Central Hospital, Songyuan, China.
Guang ZhaoDepartment of Orthopedics, The Fourth Affiliated Hospital of China Medical University, Shenyang, China.
Yanjun GaoDepartment of Orthopedics, The Fourth Affiliated Hospital of China Medical University, Shenyang, China.
Zhigang JiangDepartment of Hand Surgery, Changchun Central Hospital, Changchun, China.
Fusheng YuanDepartment of Orthopedics, The Fourth Affiliated Hospital of China Medical University, Shenyang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

At present, the main treatment methods of osteosarcoma are chemotherapy and surgery. Its 5-year survival rate has not been significantly improved in the past decades. Osteosarcoma has extremely complex multigenomic heterogeneity and lacks universally applicable signal blocking targets. Osteosarcoma is often found in adolescents or children under the age of 20, so it is very important to explore its genetic pathogenic factors. We used known osteosarcoma-related genes and computer algorithms to find more osteosarcoma pathogenic genes, laying the foundation for the treatment of osteosarcoma immune microenvironment-related treatments, so as to carry out further explorations on these genes. It is a traditional method to identify osteosarcoma related genes by collecting clinical samples, measuring gene expressions by RNA-seq technology and comparing differentially expressed gene. The high cost and time consumption make it difficult to carry out research on a large scale. In this paper, we developed a novel method "RELM" which fuses multiple extreme learning machines (ELM) to identify osteosarcoma pathogenic genes. The AUC and AUPR of RELM are 0.91 and 0.88, respectively, in 10-cross validation, which illustrates the reliability of RELM.

Indexed as

fuses multiple extreme learning machineIndex Term-osteosarcomalarge scale identificationmachine learningpathogenic genes

Identifiers

PMID34646831
PMCPMC8502917

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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.