Evidence map›Paper›PMID 35588743›Full record

ArticleCurrent biology : CB2022

Mixing genome annotation methods in a comparative analysis inflates the apparent number of lineage-specific genes.

Caroline M Weisman, Andrew W Murray, Sean R Eddy

Abstract read
In one paragraph

Article in Current biology : CB, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing 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

60 citing papers in PubMed.

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  13. Genomic, Proteomic, and Biochemical Study ofJournal of agricultural and food chemistry · 2025
    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

3 authors.

Caroline M WeismanLewis-Sigler Institute for Integrative Genomics, Carl Icahn Laboratory, Princeton University, South Drive, Princeton, NJ 08540, USA. Electronic address: cweisman@princeton.edu.
Andrew W MurrayDepartment of Molecular & Cellular Biology, Harvard University, Divinity Avenue, Cambridge, MA 02138, USA.
Sean R EddyDepartment of Molecular & Cellular Biology, Harvard University, Divinity Avenue, Cambridge, MA 02138, USA; Howard Hughes Medical Institute, Jones Bridge Road, Chevy Chase, MD 20815, USA; John A. Paulson School of Engineering and Applied Sciences, Harvard University, Oxford Street, Cambridge, MA 02138, USA.

Funding

FEEDBACK CONTROL OF THE CELL CYCLER01GM043987 · NIGMS · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI MURRAY, ANDREW W · 1990 to 2023
$6.4M
HMMER and Infernal: Finding distant homologs of sequences and RNA structuresR01HG009116 · NHGRI · HARVARD UNIVERSITY · PI EDDY, SEAN R · 2016 to 2025
$4.3M
NHGRI NIH HHS R01 HG009116NIGMS NIH HHS R01 GM043987
6 · The paper itself

Abstract

Comparisons of genomes of different species are used to identify lineage-specific genes, those genes that appear unique to one species or clade. Lineage-specific genes are often thought to represent genetic novelty that underlies unique adaptations. Identification of these genes depends not only on genome sequences, but also on inferred gene annotations. Comparative analyses typically use available genomes that have been annotated using different methods, increasing the risk that orthologous DNA sequences may be erroneously annotated as a gene in one species but not another, appearing lineage specific as a result. To evaluate the impact of such "annotation heterogeneity," we identified four clades of species with sequenced genomes with more than one publicly available gene annotation, allowing us to compare the number of lineage-specific genes inferred when differing annotation methods are used to those resulting when annotation method is uniform across the clade. In these case studies, annotation heterogeneity increases the apparent number of lineage-specific genes by up to 15-fold, suggesting that annotation heterogeneity is a substantial source of potential artifact.

Indexed as

GenomeBase SequenceMolecular Sequence Annotationgenome annotationlineage-specific genesnovel genesorphan genestaxonomically restricted genes

Identifiers

PMID35588743
PMCPMC9346927

What Socratic holds

Textmetadata
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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 Socratic graph.