Evidence map›Paper›PMID 33796851›Full record

ArticleNAR genomics and bioinformatics2021

Jonckheere-Terpstra-Kendall-based non-parametric analysis of temporal differential gene expression.

Hitoshi Iuchi, Michiaki Hamada

Abstract read
In one paragraph

Article in NAR genomics and bioinformatics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Hitoshi IuchiComputational Bio Big-Data Open Innovation Laboratory, National Institute of Advanced Industrial Science and Technology, Okubo, Shinjuku-ku, Tokyo 169-8555, Japan.ORCID https://orcid.org/0000-0002-2278-3443
Michiaki HamadaComputational Bio Big-Data Open Innovation Laboratory, National Institute of Advanced Industrial Science and Technology, Okubo, Shinjuku-ku, Tokyo 169-8555, Japan.ORCID https://orcid.org/0000-0001-9466-1034

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Time-course experiments using parallel sequencers have the potential to uncover gradual changes in cells over time that cannot be observed in a two-point comparison. An essential step in time-series data analysis is the identification of temporal differentially expressed genes (TEGs) under two conditions (e.g. control versus case). Model-based approaches, which are typical TEG detection methods, often set one parameter (e.g. degree or degree of freedom) for one dataset. This approach risks modeling of linearly increasing genes with higher-order functions, or fitting of cyclic gene expression with linear functions, thereby leading to false positives/negatives. Here, we present a Jonckheere-Terpstra-Kendall (JTK)-based non-parametric algorithm for TEG detection. Benchmarks, using simulation data, show that the JTK-based approach outperforms existing methods, especially in long time-series experiments. Additionally, application of JTK in the analysis of time-series RNA-seq data from seven tissue types, across developmental stages in mouse and rat, suggested that the wave pattern contributes to the TEG identification of JTK, not the difference in expression levels. This result suggests that JTK is a suitable algorithm when focusing on expression patterns over time rather than expression levels, such as comparisons between different species. These results show that JTK is an excellent candidate for TEG detection.

Identifiers

PMID33796851
PMCPMC7991226

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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.