An outlier approach: advancing diagnosis of neurological diseases through integrating proteomics into multi-omics guided exome reanalysis

Neurodevelopmental disorders (NDDs) often have unknown genetic causes. Current efforts in identifying disease-related genetic variants using exome or genome sequencing still lead to an excessive number of variants of uncertain significance (VUS). There is an increasing interest in transcriptomics and, more recently, proteomics for variant detection and interpretation. In this study, we integrated quantitative liquid chromatography-mass spectrometry proteomics, RNA sequencing, and exome reanalysis to resolve VUS and detect novel causal variants in 34 patients with undiagnosed NDDs, using the software PROTRIDER and DROP to detect protein outliers and RNA outliers, respectively. We obtained a diagnosis in 11 cases (32%) resulting from the increased amount of information provided by the two additional levels of omics (n = 5) and the updated literature evidence (n = 6). Our experience suggests the potential of this outlier-detection multi-omics workflow for improving diagnostic yield in NDDs and other rare disorders.

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Publication Details

Journal
npj Genomic Medicine
Published
2025-05-03
DOI
https://doi.org/10.1038/s41525-025-00493-5
Citations
7
Primary Topic
Genomics and Rare Diseases
Type
article
Field-Weighted Citation Impact
12.72

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article

An outlier approach: advancing diagnosis of neurological diseases through integrating proteomics into multi-omics guided exome reanalysis

Julien Gagneur, Cheng‐Yoong Pang, H. Leung, Brian Hon‐Yin Chung et al.
7 citations
npj Genomic Medicine
Genomics and Rare Diseases
12.72
article

An outlier approach: advancing diagnosis of neurological diseases through integrating proteomics into multi-omics guided exome reanalysis

Julien Gagneur, Cheng‐Yoong Pang, H. Leung, Brian Hon‐Yin Chung, Christopher Chun Yu Mak, Anna Ka‐Yee Kwong, Martin Man Chun Chui, Ines F. Scheller, Vicente A. Yépez, Sheila Suet-Na Wong, Cheuk‐Wing Fung
article en
7 citations

Abstract

Neurodevelopmental disorders (NDDs) often have unknown genetic causes. Current efforts in identifying disease-related genetic variants using exome or genome sequencing still lead to an excessive number of variants of uncertain significance (VUS). There is an increasing interest in transcriptomics and, more recently, proteomics for variant detection and interpretation. In this study, we integrated quantitative liquid chromatography-mass spectrometry proteomics, RNA sequencing, and exome reanalysis to resolve VUS and detect novel causal variants in 34 patients with undiagnosed NDDs, using the software PROTRIDER and DROP to detect protein outliers and RNA outliers, respectively. We obtained a diagnosis in 11 cases (32%) resulting from the increased amount of information provided by the two additional levels of omics (n = 5) and the updated literature evidence (n = 6). Our experience suggests the potential of this outlier-detection multi-omics workflow for improving diagnostic yield in NDDs and other rare disorders.

npj Genomic MedicineVol. 10(1)
Chinese University of Hong Kong (HK), Technical University of Munich (DE), University of Hong Kong (HK)
European Commission, Sugar Research and Development Corporation, University of Hong Kong, HORIZON EUROPE Framework Programme, Health and Medical Research Fund
Openalex Percentile: Top 1%
Genomics and Rare Diseases
12.72
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