Evidence map›Paper›PMID 40662828›Full record

ArticleBioinformatics (Oxford, England)2025

Generating synthetic genotypes using diffusion models.

Philip Kenneweg, Raghuram Dandinasivara, Xiao Luo, Barbara Hammer, Alexander Schönhuth

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. 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

5 authors.

Philip KennewegAG Machine Learning, Bielefeld University, Bielefeld, NRW 33615, Germany.
Raghuram DandinasivaraAG Genome Data Science, Bielefeld University, Bielefeld, NRW 33615, Germany.
Xiao LuoCollege of Biology, Hunan University, Hunan, Hunan Province 410082, China.ORCID 0000-0002-3914-359X
Barbara HammerAG Machine Learning, Bielefeld University, Bielefeld, NRW 33615, Germany.
Alexander SchönhuthAG Genome Data Science, Bielefeld University, Bielefeld, NRW 33615, Germany.ORCID 0000-0003-3529-0856

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

summaryIn this paper, we introduce the first diffusion model designed to generate complete synthetic human genotypes, which, by standard protocols, one can straightforwardly expand into full-length, DNA-level genomes. The synthetic genotypes mimic real human genotypes without just reproducing known genotypes, in terms of approved metrics. When training biomedically relevant classifiers with synthetic genotypes, accuracy is near-identical to the accuracy achieved when training classifiers with real data. We further demonstrate that augmenting small amounts of real with synthetically generated genotypes drastically improves performance rates. This addresses a significant challenge in translational human genetics: real human genotypes, although emerging in large volumes from genome wide association studies, are sensitive private data, which limits their public availability. Therefore, the integration of additional, insensitive data when striving for rapid sharing of biomedical knowledge of public interest appears imperative. AVAILABILITY AND IMPLEMENTATION: All non proprietary data and the code to replicate the experiments is available on Github.

Indexed as

GenotypeModels, GeneticAlgorithmsGenome, HumanGenome-Wide Association StudyHumans

Identifiers

PMID40662828
PMCPMC12261458

What OpenQuestion holds

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Registered trials

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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.