Evidence map›Paper›PMID 42629596›Full record

ReviewBMC genomics2026

Integrating deep learning and pangenomics to recover missing heritability from wild structural variations.

Yiquan Wang, Minnuo Cai, Yahui Ma, Aurélien Tellier, Kai Wei

Abstract readReview
In one paragraph

Review in BMC genomics, 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

5 authors.

Yiquan Wang *Xinjiang Key Laboratory of Biological Resources and Genetic Engineering, College of Life Science and Technology, Xinjiang University, Urumqi, Xinjiang, China.
Minnuo Cai *Xinjiang Key Laboratory of Biological Resources and Genetic Engineering, College of Life Science and Technology, Xinjiang University, Urumqi, Xinjiang, China.
Yahui MaXinjiang Key Laboratory of Biological Resources and Genetic Engineering, College of Life Science and Technology, Xinjiang University, Urumqi, Xinjiang, China.
Aurélien TellierPopulation Genetics, Department of Life Science Systems, School of Life Sciences, Technical University of Munich, Freising, Germany. aurelien.tellier@tum.de.
Kai WeiXinjiang Key Laboratory of Biological Resources and Genetic Engineering, College of Life Science and Technology, Xinjiang University, Urumqi, Xinjiang, China. kaiwei@xju.edu.cn.

Funding

Key Research and Development Project of Xinjiang Autonomous Region 2025B02008-1National Natural Science Foundation of China 32500528Natural Science Foundation of Xinjiang Uygur Autonomous Region 2024D01C216
6 · The paper itself

Abstract

Crop domestication has induced a severe genetic bottleneck that reduces the adaptive diversity present in modern cultivars. Standard intra-population genomic prediction models reliant on linear reference genomes and SNPs fail to capture the full spectrum of phenotypic variance hidden in wild relatives. Realizing this potential requires broadening the predictive paradigm from selection within narrow breeding populations toward evolutionary-scale inference across the entire wild-to-cultivated continuum. This missing heritability is largely sequestered within complex structural variations such as presence-absence and copy number variants. These variations drive environmental adaptations but remain obscured by reference bias. To recover these unmapped structural variations the field is evolving from linear coordinates to high-dimensional genomic data representations. We review this transition by contrasting explicit graph topologies that map reticulate evolution with implicit encodings like K-mers that capture sequence composition independent of alignment. Processing these complex and high-dimensional features necessitates advanced computational tools. We synthesize emerging deep learning frameworks and highlight how Graph Neural Networks resolve inheritance paths in topological data while Transformer-based foundation models extract functional syntax from sequence context. These architectures effectively integrate structural variations to resolve non-additive effects such as epistasis missed by traditional models. Computing these hidden structural variations facilitates the precise utilization of wild germplasm. We demonstrate how AI-driven strategies enable zero-shot prediction for uncharacterized wild alleles and optimize genotype-by-environment interactions. Ultimately these approaches pave the way for accelerated de novo domestication of climate-resilient crops.

Indexed as

Deep LearningGenetic VariationGenomicsCrops, AgriculturalGenome, PlantGraph Neural NetworksDeep learningGenomic predictionMissing heritabilityPangenomicsStructural variationWild germplasm

Identifiers

PMID42629596
PMCPMC13499299

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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.