Evidence map›Paper›PMID 28484283›Full record

ArticleScientific reports2017

Predicting influenza antigenicity from Hemagglutintin sequence data based on a joint random forest method.

Yuhua Yao, Xianhong Li, Bo Liao, Li Huang, Pingan He, Fayou Wang, Jiasheng Yang, Hailiang Sun, Yulong Zhao, Jialiang Yang

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

42 citing papers in PubMed, 71 citations in OpenAlex.

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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

10 authors at 7 institutions in 3 countries.

Yuhua YaoSchool of Mathematics and Statistics, Hainan Normal University, Haikou, 570100, P. R. China.
Xianhong LiCollege of Life Sciences, Zhejiang Sci-Tech University, Hangzhou, 310018, P. R. China.
Bo LiaoCollege of Information Science and Engineering, Hunan University, Changsha, 410082, P. R. China.
Li HuangCollege of Sciences, Zhejiang Sci-Tech University, Hangzhou, 310018, P. R. China.
Pingan HeCollege of Sciences, Zhejiang Sci-Tech University, Hangzhou, 310018, P. R. China.
Fayou WangSchool of Mathematics and Information Science, Henan Polytechnic University, Henan, 454000, P. R. China.
Jiasheng YangDepartment of Civil and Environmental Engineering, National Universality of Singapore, Singapore, 119077, Singapore.
Hailiang SunCollege of Veterinary Medicine, Huanan Agricultural University, Guangzhou, 510000, P. R. China.
Yulong ZhaoDepartment of Mathematics, City University of Hong Kong, Hong Kong, P. R. China. zhaoyulong@gmail.com.
Jialiang YangSchool of Mathematics and Statistics, Hainan Normal University, Haikou, 570100, P. R. China. jialiang.yang@mssm.edu.
Zhejiang Sci-Tech University · CNCity University of Hong Kong · HKHainan Normal University · CNHenan Polytechnic University · CNHunan University · CNIcahn School of Medicine at Mount Sinai · USSouth China Agricultural University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Timely identification of emerging antigenic variants is critical to influenza vaccine design. The accuracy of a sequence-based antigenic prediction method relies on the choice of amino acids substitution matrices. In this study, we first compared a comprehensive 95 substitution matrices reflecting various amino acids properties in predicting the antigenicity of influenza viruses by a random forest model. We then proposed a novel algorithm called joint random forest regression (JRFR) to jointly consider top substitution matrices. We applied JRFR to human H3N2 seasonal influenza data from 1968 to 2003. A 10-fold cross-validation shows that JRFR outperforms other popular methods in predicting antigenic variants. In addition, our results suggest that structure features are most relevant to influenza antigenicity. By restricting the analysis to data involving two adjacent antigenic clusters, we inferred a few key amino acids mutation driving the 11 historical antigenic drift events, pointing to experimentally validated mutations. Finally, we constructed an antigenic cartography of all H3N2 viruses with hemagglutinin (the glycoprotein on the surface of the influenza virus responsible for its binding to host cells) sequence available from NCBI flu database, and showed an overall correspondence and local inconsistency between genetic and antigenic evolution of H3N2 influenza viruses.

Indexed as

AlgorithmsAmino Acid SequenceAmino Acid SubstitutionAntigens, ViralEvolution, MolecularHemagglutinin Glycoproteins, Influenza VirusHumansInfluenza A Virus, H3N2 SubtypeMutationAntigens, ViralHemagglutinin Glycoproteins, Influenza Virus

Identifiers

PMID28484283
PMCPMC5431489
OpenAlexW2610635081

What OpenQuestion holds

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LicenceCC BY
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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 OpenQuestion graph.