Numerous web-based tools have been developed to support large-scale genomics research, whereas challenges remain due to their limited functionality. Therefore, we developed VarXOmics, an end-to-end, versatile web server for querying variants and genes, streamlining germline variant analysis, prioritizing variants with multi-omics insights, and providing interactive visualizations. The utility of VarXOmics was demonstrated by analyzing multiple small variants of the whole genome sequencing data from a breast cancer patient. It prioritized BRCA2 c.3751dup as the most likely pathogenic variant, and highlighted disease associations with cell cycle regulation, DNA repair pathways, and type 2 diabetes through multi-omics evidence, gene set enrichment, and network analysis. Overall, VarXOmics serves as a practical genomics platform for researchers and clinicians. It shows potential in identifying pathogenic variants and causal genes, uncovering the molecular mechanisms of disease pathogenesis, providing valuable references for clinical decision-making and therapeutic strategies, thus advancing precision medicine. VarXOmics is publicly available at https://www.phenomeportal.org/varxomics.
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Xinmeng Liao
Science for Life Laboratory
Xiya Song
Science for Life Laboratory
E. Green
Science for Life Laboratory
Journal of Molecular Biology
KTH Royal Institute of Technology
Science for Life Laboratory
Atatürk University
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Liao et al. (Thu,) studied this question.
synapsesocial.com/papers/69a75f2ec6e9836116a2a5dc — DOI: https://doi.org/10.1016/j.jmb.2026.169667
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