Evidence map›Paper›PMID 39568388›Full record

ReviewBriefings in functional genomics2025

Less is more: relative rank is more informative than absolute abundance for compositional NGS data.

Xubin Zheng, Nana Jin, Qiong Wu, Ning Zhang, Haonan Wu, Yuanhao Wang, Rui Luo, Tao Liu, Wanfu Ding, Qingshan Geng and 1 more

Abstract readReview
In one paragraph

Review in Briefings in functional genomics, 2025. 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. 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

11 authors.

Xubin ZhengGuangdong Provincial Clinical Research Center for Geriatrics, Shenzhen Clinical Research Center for Geriatrics, Shenzhen People's Hospital, Luohu District, Shenzhen 518020, China.ORCID 0000-0003-2322-857X
Nana JinGuangdong Provincial Clinical Research Center for Geriatrics, Shenzhen Clinical Research Center for Geriatrics, Shenzhen People's Hospital, Luohu District, Shenzhen 518020, China.
Qiong WuSchool of Basic Medicine, North Sichuan Medical College, Nanchong 637000, Sichuan, China.
Ning ZhangGuangdong Provincial Clinical Research Center for Geriatrics, Shenzhen Clinical Research Center for Geriatrics, Shenzhen People's Hospital, Luohu District, Shenzhen 518020, China.
Haonan WuGuangdong Provincial Clinical Research Center for Geriatrics, Shenzhen Clinical Research Center for Geriatrics, Shenzhen People's Hospital, Luohu District, Shenzhen 518020, China.
Yuanhao WangGuangdong Provincial Clinical Research Center for Geriatrics, Shenzhen Clinical Research Center for Geriatrics, Shenzhen People's Hospital, Luohu District, Shenzhen 518020, China.
Rui LuoDepartment of Systems Engineering, City University of Hong Kong, Kowloon, Hong Kong SAR.
Tao LiuInternational Digital Economy Academy (IDEA), Futian District, Shenzhen 518020, China.
Wanfu DingGuangdong Provincial Clinical Research Center for Geriatrics, Shenzhen Clinical Research Center for Geriatrics, Shenzhen People's Hospital, Luohu District, Shenzhen 518020, China.
Qingshan GengGuangdong Provincial Clinical Research Center for Geriatrics, Shenzhen Clinical Research Center for Geriatrics, Shenzhen People's Hospital, Luohu District, Shenzhen 518020, China.
Lixin ChengGuangdong Provincial Clinical Research Center for Geriatrics, Shenzhen Clinical Research Center for Geriatrics, Shenzhen People's Hospital, Luohu District, Shenzhen 518020, China.ORCID 0000-0002-9427-383X

Funding

National Natural Science Foundation of China 32370711Shenzhen Medical Research Funds A2303033Shenzhen Science and Technology Program RKX20220705152810024
6 · The paper itself

Abstract

High-throughput gene expression data have been extensively generated and utilized in biological mechanism investigations, biomarker detection, disease diagnosis and prognosis. These applications encompass not only bulk transcriptome, but also single cell RNA-seq data. However, extracting reliable biological information from transcriptome data remains challenging due to the constrains of Compositional Data Analysis. Current data preprocessing methods, including dataset normalization and batch effect correction, are insufficient to address these issues and improve data quality for downstream analysis. Alternatively, qualification methods focusing on the relative order of gene expression (ROGER) are more informative than the quantification methods that rely on gene expression abundance. The Pairwise Analysis of Gene expression method is an enhancement of ROGER, designed for data integration in either sample space or feature space. In this review, we summarize the methods applied to transcriptome data analysis and discuss their potentials in predicting clinical outcomes.

Indexed as

Gene Expression ProfilingHigh-Throughput Nucleotide SequencingTranscriptomeComputational BiologyHumanscompositional data analysisdata integrationpairwise analysisrelative expressiontranscriptome

Identifiers

PMID39568388
PMCPMC11735744

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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.