Evidence map›Paper›PMID 39344923›Full record

ArticleGenetic epidemiology2025

Enhancing Gene Expression Predictions Using Deep Learning and Functional Annotations.

Pratik Ramprasad, Jingchen Ren, Wei Pan

Abstract read
In one paragraph

Article in Genetic epidemiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Review
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.

Pratik RamprasadDivision of Biostatistics and Health Data Science, University of Minnesota, Minneapolis, Minnesota, USA.ORCID http://orcid.org/0009-0007-1477-6490
Jingchen RenDivision of Biostatistics and Health Data Science, University of Minnesota, Minneapolis, Minnesota, USA.
Wei PanDivision of Biostatistics and Health Data Science, University of Minnesota, Minneapolis, Minnesota, USA.ORCID https://orcid.org/0000-0002-1159-0582

Funding

Causal and integrative deep learning for Alzheimer's disease geneticsU01AG073079 · NIA · UNIVERSITY OF MINNESOTA · PI PAN, WEI · 2021 to 2025
$3.5M
Deep Learning with Neuroimaging Genetic Data for Alzheimer's DiseaseR01AG069895 · NIA · UNIVERSITY OF MINNESOTA · PI PAN, WEI, SHEN, XIAOTONG TOM · 2020 to 2024
$3.4M
Discovering causal genes, brain regions and other risk factors for Alzheimer's DiseaseR01AG065636 · NIA · UNIVERSITY OF MINNESOTA · PI PAN, WEI · 2020 to 2024
$3.1M
Integrating Alzheimer's disease GWAS with proteomic and metabolomic QTL dataRF1AG067924 · NIA · UNIVERSITY OF MINNESOTA · PI PAN, WEI · 2020 to 2020
$1.9M
Integrating Alzheimer's disease GWAS with proteomic and metabolomic QTL dataR01AG067924 · NIA · UNIVERSITY OF MINNESOTA · PI PAN, WEI · 2024 to 2024
$465k
NIA NIH HHS R01 AG065636NIA NIH HHS R01 AG067924NIA NIH HHS R01 AG069895NIA NIH HHS RF1 AG067924NIA NIH HHS U01 AG073079This research was supported by NIH grants U01 AG073079, R01 AG065636, R01 AG069895, and RF1 AG067924, and by the Minnesota Supercomputing Institute at the University of Minnesota. The Genotype-Tissue Expression (GTEx) Project was supported by the Common Fund of the Office of the Director of the National Institutes of Health, and by NCI, NHGRI, NHLBI, NIDA, NIMH, and NINDS; the GTEx data were obtained from dbGaP Project #26511.
6 · The paper itself

Abstract

Transcriptome-wide association studies (TWAS) aim to uncover genotype-phenotype relationships through a two-stage procedure: predicting gene expression from genotypes using an expression quantitative trait locus (eQTL) data set, then testing the predicted expression for trait associations. Accurate gene expression prediction in stage 1 is crucial, as it directly impacts the power to identify associations in stage 2. Currently, the first stage of such studies is primarily conducted using linear models like elastic net regression, which fail to capture the nonlinear relationships inherent in biological systems. Deep learning methods have the potential to model such nonlinear effects, but have yet to demonstrably outperform linear methods at this task. To address this gap, we propose a new deep learning architecture to predict gene expression from genotypic variation across individuals. Our method utilizes a learnable input scaling layer in conjunction with a convolutional encoder to capture nonlinear effects and higher-order interactions without compromising on interpretability. We further augment this approach to allow for parameter sharing across multiple networks, enabling us to utilize prior information for individual variants in the form of functional annotations. Evaluations on real-world genomic data show that our method consistently outperforms elastic net regression across a large set of heritable genes. Furthermore, our model statistically significantly improved predictive performance by leveraging functional annotations, whereas elastic net regression failed to show equivalent gains when using the same information, suggesting that our method can capture nonlinear functional information beyond the capability of linear models.

Indexed as

Deep LearningQuantitative Trait LociGene ExpressionGenome-Wide Association StudyGenotypeHumansModels, GeneticPhenotypePolymorphism, Single NucleotideTranscriptomeconvolutional neural networkseQTLsfunctional annotationsgene expression predictionTWAS

Identifiers

PMID39344923
PMCPMC11656135

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.