Evidence map›Paper›PMID 40837840›Full record

ArticleNAR genomics and bioinformatics2025

Explicit Scale Simulation for analysis of RNA-sequencing count data with ALDEx2.

Gregory B Gloor, Michelle Pistner Nixon, Justin D Silverman

Abstract read
In one paragraph

Article in NAR genomics and bioinformatics, 2025. 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.

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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

3 authors.

Gregory B GloorDepartment of Biochemistry, University of Western Ontario, London ON, N6A 5C1, Canada.ORCID https://orcid.org/0000-0001-5803-3380
Michelle Pistner NixonDepartment of Population Health Sciences, Geisinger, Danville, PA 17822, United States.
Justin D SilvermanCollege of Information Sciences and Technology, Pennsylvania State University, University Park, PA 16802, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In high-throughput sequencing (HTS) studies, sample-to-sample variation in sequencing depth is driven by technical factors, and not by variation in the scale (size) of the biological system. Typically a statistical normalization removes unwanted technical variation in the data or the parameters of the model to enable differential abundance analyses. We recently showed that all normalizations make implicit assumptions about the unmeasured system scale and that errors in these assumptions can dramatically increase false positive and false negative rates. We demonstrated that these errors can be mitigated by accounting for uncertainty using a

Indexed as

Gene Expression ProfilingSequence Analysis, RNASoftwareComputer SimulationHigh-Throughput Nucleotide SequencingHumansTranscriptome

Identifiers

PMID40837840
PMCPMC12362245

What OpenQuestion holds

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LicenceCC BY
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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.