Evidence map›Paper›PMID 38965388›Full record

ArticleScientific reports2024

Comprehensive application of AI algorithms with TCR NGS data for glioma diagnosis.

Kaiyue Zhou, Zhengliang Xiao, Qi Liu, Xu Wang, Jiaxin Huo, Xiaoqi Wu, Xiaoxiao Zhao, Xiaohan Feng, Baoyi Fu, Pengfei Xu and 4 more

Abstract read
In one paragraph

Article in Scientific reports, 2024. 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

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

2 citing papers in PubMed.

  1. Article
  2. Review
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

14 authors.

Kaiyue ZhouDepartment of Mathematics, School of Mathematical Sciences, Inner Mongolia University, Hohhot, China.
Zhengliang XiaoDepartment of Mathematics, School of Mathematical Sciences, Inner Mongolia University, Hohhot, China.
Qi LiuDepartment of Mathematics, School of Mathematical Sciences, Inner Mongolia University, Hohhot, China.
Xu WangDepartment of Mathematics, School of Mathematical Sciences, Inner Mongolia University, Hohhot, China.
Jiaxin HuoDepartment of Mathematics, School of Mathematical Sciences, Inner Mongolia University, Hohhot, China.
Xiaoqi WuDepartment of Mathematics, School of Mathematical Sciences, Inner Mongolia University, Hohhot, China.
Xiaoxiao ZhaoDepartment of Mathematics, School of Mathematical Sciences, Inner Mongolia University, Hohhot, China.
Xiaohan FengDepartment of Mathematics, School of Mathematical Sciences, Inner Mongolia University, Hohhot, China.
Baoyi FuDepartment of Mathematics, School of Mathematical Sciences, Inner Mongolia University, Hohhot, China.
Pengfei XuHangzhou ImmuQuad Biotechnologies, LLC, Hangzhou, China.
Yunyun DengHangzhou ImmuQuad Biotechnologies, LLC, Hangzhou, China.
Wenwen XiaoHangzhou ImmuQuad Biotechnologies, LLC, Hangzhou, China.
Tao SunHangzhou ImmuQuad Biotechnologies, LLC, Hangzhou, China. taosun@immuquad.com.
Lin DaDepartment of Mathematics, School of Mathematical Sciences, Inner Mongolia University, Hohhot, China. 111977331@imu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

T-cell receptor (TCR) detection can examine the extent of T-cell immune responses. Therefore, the article analyzed characteristic data of glioma obtained by DNA-based TCR high-throughput sequencing, to predict the disease with fewer biomarkers and higher accuracy. We downloaded data online and obtained six TCR-related diversity indices to establish a multidimensional classification system. By comparing actual presence of the 602 correlated sequences, we obtained two-dimensional and multidimensional datasets. Multiple classification methods were utilized for both datasets with the classification accuracy of multidimensional data slightly less to two-dimensional datasets. This study reduced the TCR β sequences through feature selection methods like RFECV (Recursive Feature Elimination with Cross-Validation). Consequently, using only the presence of these three sequences, the classification AUC value of 96.67% can be achieved. The combination of the three correlated TCR clones obtained at a source data threshold of 0.1 is: CASSLGGNTEAFF_TRBV12_TRBJ1-1, CASSYSDTGELFF_TRBV6_TRBJ2-2, and CASSLTGNTEAFF_TRBV12_TRBJ1-1. At 0.001, the combination is: CASSLGETQYF_TRBV12_TRBJ2-5, CASSLGGNQPQHF_TRBV12_TRBJ1-5, and CASSLSGNTIYF_TRBV12_TRBJ1-3. This method can serve as a potential diagnostic and therapeutic tool, facilitating diagnosis and treatment of glioma and other cancers.

Indexed as

AlgorithmsGliomaHigh-Throughput Nucleotide SequencingReceptors, Antigen, T-CellBrain NeoplasmsHumansReceptors, Antigen, T-CellArtificial intelligence techniquesFeature selection methodsGliomaPrognosisT-cell repertoire (TCR)

Identifiers

PMID38965388
PMCPMC11224284

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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.