Evidence map›Paper›PMID 40166296›Full record

ArticlebioRxiv : the preprint server for biology2025

Domain-specific embeddings uncover latent genetics knowledge.

S S Ho, R E Mills

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. 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

2 authors.

S S HoDepartment of Human Genetics, University of Michigan, Ann Arbor, MI, USA.ORCID 0000-0002-6685-774X
R E MillsDepartment of Human Genetics, University of Michigan, Ann Arbor, MI, USA.ORCID 0000-0003-3425-6998

Funding

PREDOCTORAL TRAINING IN GENETICST32GM007544 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MORAN, JOHN V. · 1985 to 2022
$11.3M
NIGMS NIH HHS T32 GM007544
6 · The paper itself

Abstract

The inundating rate of scientific publishing means every researcher will miss new discoveries from overwhelming saturation. To address this limitation, we employ natural language processing to overcome human limitations in reading, curation, and knowledge synthesis, with domain-specific applications to genetics and genomics. We construct a corpus of 3.5 million normalized genetics and genomics abstracts and implement both semantic and network-based embedding models. Our methods not only capture broad biological concepts and relationships but also predict complex phenomena such as gene expression. Through a rigorous temporal validation framework, we demonstrate that our embeddings successfully predict gene-disease associations, cancer driver genes, and experimentally-verified protein interactions years before their formal documentation in literature. Additionally, our embeddings successfully predict experimentally verified gene-gene interactions absent from the literature. These findings demonstrate that substantial undiscovered knowledge exists within the collective scientific literature and that computational approaches can accelerate biological discovery by identifying hidden connections across the fragmented landscape of scientific publishing.

Identifiers

PMID40166296
PMCPMC11957060

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.