Evidence map›Paper›PMID 29658777›Full record

ArticleJournal of computational biology : a journal of computational molecular cell biology2018

Simple Comparative Analyses of Differentially Expressed Gene Lists May Overestimate Gene Overlap.

Chelsea M Lawhorn, Rachel Schomaker, Jonathan T Rowell, Olav Rueppell

Abstract readComparative Study
In one paragraph

Article in Journal of computational biology : a journal of computational molecular cell biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 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

4 authors.

Chelsea M Lawhorn1 Department of Mathematics, Winthrop University , Rock Hill, South Carolina.
Rachel Schomaker2 Department of Biology, Florida Southern College , Lakeland, Florida.
Jonathan T Rowell3 Department of Mathematics and Statistics, University of North Carolina at Greensboro , Greensboro, North Carolina.
Olav Rueppell4 Department of Biology, University of North Carolina at Greensboro , Greensboro, North Carolina.

Funding

Genomic Analyses of Intraspecific Patterns of Extreme Recombination in Honey BeesR15GM102753 · NIGMS · UNIVERSITY OF NORTH CAROLINA GREENSBORO · PI RUEPPELL, OLAV · 2012 to 2012
$287k
NIGMS NIH HHS R15 GM102753
6 · The paper itself

Abstract

Comparing the overlap between sets of differentially expressed genes (DEGs) within or between transcriptome studies is regularly used to infer similarities between biological processes. Significant overlap between two sets of DEGs is usually determined by a simple test. The number of potentially overlapping genes is compared to the number of genes that actually occur in both lists, treating every gene as equal. However, gene expression is controlled by transcription factors that bind to a variable number of transcription factor binding sites, leading to variation among genes in general variability of their expression. Neglecting this variability could therefore lead to inflated estimates of significant overlap between DEG lists. With computer simulations, we demonstrate that such biases arise from variation in the control of gene expression. Significant overlap commonly arises between two lists of DEGs that are randomly generated, assuming that the control of gene expression is variable among genes but consistent between corresponding experiments. More overlap is observed when transcription factors are specific to their binding sites and when the number of genes is considerably higher than the number of different transcription factors. In contrast, overlap between two DEG lists is always lower than expected when the genetic architecture of expression is independent between the two experiments. Thus, the current methods for determining significant overlap between DEGs are potentially confounding biologically meaningful overlap with overlap that arises due to variability in control of expression among genes, and more sophisticated approaches are needed.

Indexed as

Gene Expression RegulationGenetic VariationTranscriptomeComputer SimulationGene Expression ProfilingHumansTranscription FactorsTranscription Factorsdifferentially expressed genesgene regulationgenetic architecturetranscription factor binding sitestranscriptome

Identifiers

PMID29658777
PMCPMC5998827

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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.