Evidence map›Paper›PMID 41028272›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2026

Bioinformatics Analysis of Transcriptomic Data (Bulk and scRNA-Seq) for Immuno-Oncology.

Mai Hanh Nguyen, Nguyen Quoc Khanh Le

Abstract read
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In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

2 authors.

Mai Hanh NguyenInternational Ph.D. Program in Cell Therapy and Regenerative Medicine, College of Medicine, Taipei Medical University, Taipei, Taiwan.
Nguyen Quoc Khanh LeAIBioMed Research Group, Taipei Medical University, Taipei, Taiwan. khanhlee@tmu.edu.tw.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bioinformatics plays a pivotal role in immunology by enabling the analysis of large-scale datasets generated from high-throughput technologies, such as next-generation sequencing (NGS), single-cell RNA sequencing (scRNA-seq), and mass cytometry. These methods provide deep insights into immune system dynamics, helping to decode immune cell heterogeneity, gene expression patterns, and immune receptor repertoires. Key bioinformatics approaches include transcriptomic analysis to identify immune-related gene signatures, single-cell sequencing tools for profiling immune cell states, immune repertoire analysis to understand T-cell and B-cell diversity, and multiomics integration to uncover regulatory networks. By leveraging these methods, researchers can better understand immune responses in health and disease, identify therapeutic targets, and develop precision immunotherapies. This chapter will offer a comprehensive guide to the essential bioinformatics tools and techniques used in immunological research, facilitating effective data analysis and interpretation.

Indexed as

Computational BiologyGene Expression ProfilingNeoplasmsRNA-SeqSingle-Cell AnalysisTranscriptomeHigh-Throughput Nucleotide SequencingHumansSequence Analysis, RNASingle-Cell Gene Expression AnalysisBioinformaticsImmunologyImmunotherapyOncologyTranscriptomic

Identifiers

What OpenQuestion holds

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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.