Evidence map›Paper›PMID 37216599›Full record

ArticleNucleic acids research2023

NORMSEQ: a tool for evaluation, selection and visualization of RNA-Seq normalization methods.

Chantal Scheepbouwer, Michael Hackenberg, Monique A J van Eijndhoven, Alan Gerber, Michiel Pegtel, Cristina Gómez-Martín

Abstract read
In one paragraph

Article in Nucleic acids research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. The circadian isoform landscape of mouse livers.NAR genomics and bioinformatics · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Article
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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

6 authors.

Chantal ScheepbouwerDepartment of Neurosurgery, Cancer Center Amsterdam, Amsterdam University Medical Center (UMC) location Vrije Universiteit Amsterdam, Amsterdam 1081HV, The Netherlands.ORCID 0000-0003-4243-0095
Michael HackenbergGenetics Genetics Department, Faculty of Science, Universidad de Granada, Campus de Fuentenueva s/n, 18071, Granada, Spain.ORCID 0000-0003-2248-3114
Monique A J van EijndhovenDepartment of Pathology, Cancer Center Amsterdam, Amsterdam UMC location Vrije Universiteit Amsterdam, Amsterdam 1081HV, The Netherlands.
Alan GerberDepartment of Neurosurgery, Cancer Center Amsterdam, Amsterdam University Medical Center (UMC) location Vrije Universiteit Amsterdam, Amsterdam 1081HV, The Netherlands.ORCID 0000-0003-3909-3606
Michiel PegtelDepartment of Pathology, Cancer Center Amsterdam, Amsterdam UMC location Vrije Universiteit Amsterdam, Amsterdam 1081HV, The Netherlands.ORCID 0000-0002-7357-4406
Cristina Gómez-MartínDepartment of Pathology, Cancer Center Amsterdam, Amsterdam UMC location Vrije Universiteit Amsterdam, Amsterdam 1081HV, The Netherlands.ORCID 0000-0003-0866-4103

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

RNA-sequencing has become one of the most used high-throughput approaches to gain knowledge about the expression of all different RNA subpopulations. However, technical artifacts, either introduced during library preparation and/or data analysis, can influence the detected RNA expression levels. A critical step, especially in large and low input datasets or studies, is data normalization, which aims at eliminating the variability in data that is not related to biology. Many normalization methods have been developed, each of them relying on different assumptions, making the selection of the appropriate normalization strategy key to preserve biological information. To address this, we developed NormSeq, a free web-server tool to systematically assess the performance of normalization methods in a given dataset. A key feature of NormSeq is the implementation of information gain to guide the selection of the best normalization method, which is crucial to eliminate or at least reduce non-biological variability. Altogether, NormSeq provides an easy-to-use platform to explore different aspects of gene expression data with a special focus on data normalization to help researchers, even without bioinformatics expertise, to obtain reliable biological inference from their data. NormSeq is freely available at: https://arn.ugr.es/normSeq.

Indexed as

Gene Expression ProfilingRNA-SeqSoftwareGene LibraryRNASequence Analysis, RNARNA

Identifiers

PMID37216599
PMCPMC10320083

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.