Evidence map›Paper›PMID 41604548›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2026

CLinNET: An Interpretable and Uncertainty-Aware Deep Learning Framework for Multi-Modal Clinical Genomics.

Ivan Bakhshayeshi, Mohammad Mahdi Hosseini, Ahmadreza Argha, Roxana Zahedi, Nigel H Lovell, Hamid Alinejad-Rokny

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2026. 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. Review
  2. Article
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

6 authors.

Ivan BakhshayeshiUNSW BioMedical Machine Learning Lab (BML), School of Biomedical Engineering, UNSW Sydney, Sydney, NSW, 2052, Australia.
Mohammad Mahdi HosseiniRemote Internship in UNSW BioMedical Machine Learning Lab, School of Biomedical Engineering, UNSW Sydney, Sydney, NSW, 2052, Australia.
Ahmadreza ArghaSchool of Biomedical Engineering, UNSW Sydney, Sydney, NSW, 2052, Australia.
Roxana ZahediUNSW BioMedical Machine Learning Lab (BML), School of Biomedical Engineering, UNSW Sydney, Sydney, NSW, 2052, Australia.
Nigel H LovellSchool of Biomedical Engineering, UNSW Sydney, Sydney, NSW, 2052, Australia.
Hamid Alinejad-RoknyUNSW BioMedical Machine Learning Lab (BML), School of Biomedical Engineering, UNSW Sydney, Sydney, NSW, 2052, Australia.

Funding

University of New South Wales P23453233
6 · The paper itself

Abstract

Identifying molecular drivers and diagnostic genes for neurocognitive disorders (NDs) remains a major challenge due to the prevalence of variants of uncertain significance (VUS) and limitations in current diagnostic platforms. While artificial intelligence (AI) offers potential solutions, existing models often lack interpretability and fail to address uncertainty, limiting clinical utility. CLinNET, a multi-modal deep neural network with a dual-branch design integrating sequencing data, gene expression, biological pathways, and gene ontology (GO) is introduced to enhance gene curation and VUS interpretation. CLinNET employs a biologically informed architecture, confidence-based uncertainty quantification, and layer-wise SHapley Additive exPlanations (SHAP) for robust interpretability. Its sparse networks, enriched with pathway and GO data, prioritize tissue-expressed genes to improve prediction accuracy and biological relevance. Trained on ND datasets, CLinNET outperformed existing methods with an F1-score of 76.4%, accuracy of 77.2%, and area under the precision-recall curve (AUC-PR) of 84%. Incorporating uncertainty filtering further improved precision to 87% while retaining 73% of predictions as high-confidence. CLinNET identified significantly more ND-associated genes than random permutations, with minimal overlap with cardiovascular-associated genes, confirming specificity. Among the top decile of ranked genes, 78 were linked to NDs (p-value = 1.2e-11), and 372 to rare diseases involving nervous system abnormalities, highlighting their diagnostic potential. CLinNET's validation in prostate cancer datasets underscores its adaptability, positioning it as a robust tool for individualized medicine.

Indexed as

Deep LearningGenomicsHumansUncertaintycopy number variantsdeep learninggene curationinterpretabilityneurocognitive disordersuncertainty quantification

Identifiers

PMID41604548
PMCPMC12948272

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.