Evidence map›Paper›PMID 42366621›Full record

ReviewBriefings in bioinformatics2026

Evaluating completeness, coherence, and consistency of genome-scale function annotations.

Rund Tawfiq, Maxat Kulmanov, Robert Hoehndorf

Abstract readReview
In one paragraph

Review in Briefings in bioinformatics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Rund TawfiqBiological and Environmental Sciences & Engineering (BESE) Division, King Abdullah University of Science and Technology, 4700 KAUST, Thuwal 23955, Saudi Arabia.ORCID 0000-0002-7052-573X
Maxat KulmanovKAUST Center of Excellence for Smart Health (KCSH), King Abdullah University of Science and Technology, 4700 KAUST, Thuwal 23955, Saudi Arabia.ORCID 0000-0003-1710-1820
Robert HoehndorfBiological and Environmental Sciences & Engineering (BESE) Division, King Abdullah University of Science and Technology, 4700 KAUST, Thuwal 23955, Saudi Arabia.ORCID 0000-0001-8149-5890

Funding

KAUST Supercomputing LaboratoryKing Abdullah University of Science and Technology (KAUST)-Center of Excellence for Generative AI 5940King Abdullah University of Science and Technology (KAUST)-KAUST Center of Excellence for Smart Health (KCSH) 5932King Abdullah University of Science and Technology (KAUST) Office of Sponsored Research (OSR) REI/1/4938-01-01King Abdullah University of Science and Technology (KAUST) Office of Sponsored Research (OSR) REI/1/5235-01-01King Abdullah University of Science and Technology (KAUST) Office of Sponsored Research (OSR) REI/1/5659-01-01King Abdullah University of Science and Technology (KAUST) Office of Sponsored Research (OSR) URF/1/5041-01-01
6 · The paper itself

Abstract

Protein function annotation traditionally follows a reductionist approach, assigning functions to individual proteins acting in isolation. This treats each annotation as an independent fact, disconnected from the broader biological system. However, proteins operate within integrated networks where their functions depend on genomic context and interacting partners. This needs to be reflected in function annotation and evaluation frameworks. We assess whether annotated protein functions could plausibly coexist within a living organism. To achieve this goal, we formalize three criteria grounded in systems biology principles: completeness (presence of essential functions), coherence (satisfaction of functional dependencies), and consistency (absence of mutually exclusive functions). We applied this framework to manually curated function annotations from six model organisms and computational function predictions from seven methods. While model organism annotations largely satisfied our constraints, computational function prediction methods systematically failed to produce biologically plausible genome-scale annotations. Our review reveals a measurable gap between the per-protein objectives of current annotation methods and the system-level criteria that an annotation set must satisfy to describe a viable organism. Our evaluation framework grounded in systems biology principles provides quantitative metrics for evaluating biological plausibility and establishes a foundation for developing system-aware annotation approaches. Augmenting protein-level annotation with system-level criteria offers a tractable path to improving annotation of the rapidly growing collection of sequenced genomes and metagenomes.

Indexed as

GenomeMolecular Sequence AnnotationProteinsComputational BiologyGenomicsSystems BiologyProteinsfunctional genomicsGene Ontologyprotein functionsystems biology

Identifiers

PMID42366621
PMCPMC13310775

What Socratic holds

Textmetadata
LicenceCC BY
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.