Evidence map›Paper›PMID 39624165›Full record

ReviewComputational and structural biotechnology journal2024

Review and revamp of compositional data transformation: A new framework combining proportion conversion and contrast transformation.

Yiqian Zhang, Jonas Schluter, Lijun Zhang, Xuan Cao, Robert R Jenq, Hao Feng, Jonathan Haines, Liangliang Zhang

Abstract readReview
In one paragraph

Review in Computational and structural biotechnology journal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Frontiers in microbiology · 2026
    Article
  5. Article
  6. 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

8 authors.

Yiqian ZhangDepartment of Population and Quantitative Health Sciences, Case Western Reserve University, 2109 Adelbert Rd, Cleveland, 44106, OH, USA.
Jonas SchluterInstitute for Systems Genetics, Department of Microbiology, New York University Grossman School of Medicine, 435 East 30th Street, New York, 10016, NY, USA.
Lijun ZhangDepartment of Population and Quantitative Health Sciences, Case Western Reserve University, 2109 Adelbert Rd, Cleveland, 44106, OH, USA.
Xuan CaoDivision of Statistics and Data Science, Department of Mathematical Sciences, University of Cincinnati, 2815 Commons Way, Cincinnati, 45219, OH, USA.
Robert R JenqDepartment of Hematology & Hematopoietic Cell Transplantation, City of Hope, 1500 East Duarte Road, Duarte, 91010, CA, USA.
Hao FengDepartment of Population and Quantitative Health Sciences, Case Western Reserve University, 2109 Adelbert Rd, Cleveland, 44106, OH, USA.
Jonathan HainesDepartment of Population and Quantitative Health Sciences, Case Western Reserve University, 2109 Adelbert Rd, Cleveland, 44106, OH, USA.
Liangliang ZhangDepartment of Population and Quantitative Health Sciences, Case Western Reserve University, 2109 Adelbert Rd, Cleveland, 44106, OH, USA.

Funding

Translational and Therapeutics CoreP30AG072959 · NIA · CLEVELAND CLINIC LERNER COM-CWRU · PI Mark J Lowe · 2021 to 2026
$23.9M
NIA NIH HHS P30 AG072959
6 · The paper itself

Abstract

Due to the development of next-generation sequencing technology and an increased appreciation of their role in modulating host immunity and their potential as therapeutic agents, the human microbiome has emerged as a key area of interest in various biological investigations of human health and disease. However, microbiome data present a number of statistical challenges not addressed by existing methods, such as the varying sequencing depth, the compositionality, and zero inflation. Solutions like scaling and transformation methods help to mitigate heterogeneity and release constraints, but often introduce biases and yield inconsistent results on the same data. To address these issues, we conduct a systematic review of compositional data transformation, with a particular focus on the connection and distinction of existing techniques. Additionally, we create a new framework that enables the development of new transformations by combining proportion conversion with contrast transformations. This framework includes well-known methods such as Additive Log Ratio (ALR) and Centered Log Ratio (CLR) as special cases. Using this framework, we develop two novel transformations-Centered Arcsine Contrast (CAC) and Additive Arcsine Contrast (AAC)-which show enhanced performance in scenarios with high zero-inflation. Moreover, our findings suggest that ALR and CLR transformations are more effective when zero values are less prevalent. This comprehensive review and the innovative framework provide microbiome researchers with a significant direction to enhance data transformation procedures and improve analytical outcomes.

Indexed as

Compositional data analysisContrast transformationConversionMicrobiomeRelative abundanceZero inflation

Identifiers

PMID39624165
PMCPMC11609487

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.