Evidence map›Paper›PMID 36977685›Full record

ArticleScientific reports2023

Applying T-classifier, binary classifiers, upon high-throughput TCR sequencing output to identify cytomegalovirus exposure history.

Kaiyue Zhou, Jiaxin Huo, Caixia Gao, Xu Wang, Pengfei Xu, Jiahuan Hou, Wenying Guo, Tao Sun, Lin Da

Open access · goldFull text read
In one paragraph

Article in Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

5 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. CMV-specific clonal expansion of Th1, GZMKbioRxiv : the preprint server for biology · 2025
    Article
  3. Translational cancer research · 2025
    Article
  4. Article
  5. 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

9 authors at 1 institution in 1 country.

Kaiyue Zhou *Department of Mathematics, School of Mathematical Sciences, Inner Mongolia University, Hohhot, China.
Jiaxin Huo *Department of Mathematics, School of Mathematical Sciences, Inner Mongolia University, Hohhot, China.
Caixia GaoDepartment of Mathematics, School of Mathematical Sciences, Inner Mongolia University, Hohhot, China.
Xu WangDepartment of Mathematics, School of Mathematical Sciences, Inner Mongolia University, Hohhot, China.
Pengfei XuHangzhou ImmuQuad Biotechnologies, Hangzhou, China.
Jiahuan HouHangzhou ImmuQuad Biotechnologies, Hangzhou, China.
Wenying GuoHangzhou ImmuQuad Biotechnologies, Hangzhou, China.
Tao SunHangzhou ImmuQuad Biotechnologies, Hangzhou, China. taosun@immuquad.com.
Lin DaDepartment of Mathematics, School of Mathematical Sciences, Inner Mongolia University, Hohhot, China. 111977331@imu.edu.cn.
Inner Mongolia University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

With the continuous development of information technology and the running speed of computers, the development of informatization has led to the generation of increasingly more medical data. Solving unmet needs such as employing the constantly developing artificial intelligence technology to medical data and providing support for the medical industry is a hot research topic. Cytomegalovirus (CMV) is a kind of virus that exists widely in nature with strict species specificity, and the infection rate among Chinese adults is more than 95%. Therefore, the detection of CMV is of great importance since the vast majority of infected patients are in a state of invisible infection after the infection, except for a few patients with clinical symptoms. In this study, we present a new method to detect CMV infection status by analyzing high-throughput sequencing results of T cell receptor beta chains (TCRβ). Based on the high-throughput sequencing data of 640 subjects from cohort 1, Fisher's exact test was performed to evaluate the relationship between TCRβ sequences and CMV status. Furthermore, the number of subjects with these correlated sequences to different degrees in cohort 1 and cohort 2 were measured to build binary classifier models to identify whether the subject was CMV positive or negative. We select four binary classification algorithms: logistic regression (LR), support vector machine (SVM), random forest (RF), and linear discriminant analysis (LDA) for side-by-side comparison. According to the performance of different algorithms corresponding to different thresholds, four optimal binary classification algorithm models are obtained. The logistic regression algorithm performs best when Fisher's exact test threshold is 10

Indexed as

Artificial IntelligenceCytomegalovirus InfectionsAdultAlgorithmsCytomegalovirusHigh-Throughput Nucleotide SequencingHumansReceptors, Antigen, T-CellReceptors, Antigen, T-Cell

Identifiers

PMID36977685
PMCPMC10043529
OpenAlexW4361205833

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Registered trials

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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.