Translational bioinformatics and machine learning framework for biomarker discovery, disease prediction, and patient profiling for precision medicine
Zeeshan Ahmed, Prithvi Govindareddy, William DeGroat…·Saman Zeeshan
Author
Rutgers, The State University of New JerseyORCID 0000-0002-7839-6864Unclaimed ORCID profile · follow to get notified of new preprints
Mutual co-authors in cluster
8 papers
Recent·Most cited
Zeeshan Ahmed, Prithvi Govindareddy, William DeGroat…·Saman Zeeshan
This paper introduces MPRabc, an MPRA-informed model that improves enhancer-gene interaction prediction across cell types.
Rishabh Narayanan, Elizabeth Peker, William DeGroat…·Zeeshan Ahmed
This paper introduces 3D IntelliGenes, a tool for visualizing AI/ML results on multi-omics data to discover biomarkers and predict diseases through 3D clustering and feature analysis.
Rishabh Narayanan, William DeGroat, Elizabeth Peker…·Zeeshan Ahmed
VAREANT is a bioinformatics tool that simplifies variant data preprocessing, annotation, and AI/ML preparation for genomic analysis.
William DeGroat, Habiba Abdelhalim, Elizabeth Peker…·Zeeshan Ahmed
The paper develops a multimodal AI/ML framework to identify biomarkers and predict cardiovascular disease using multi-omics data, finding a 27-component signature with high predictive accuracy.
William DeGroat, Fumitaka Inoue, Tal Ashuach…·Anat Kreimer
The paper constructs enhancer-promoter interaction networks during neural differentiation and identifies their temporal dynamics and disease-associated variant enrichment using computational and experimental methods.
William DeGroat, Habiba Abdelhalim, Kush Patel…·Zeeshan Ahmed
This study identifies 18 significant transcriptomic biomarkers for cardiovascular disease with 96% accuracy using a combination of statistical tests and machine learning classifiers.
Zeeshan Ahmed, Saman Zeeshan, Nicholas Persaud…·Bruce T. Liang
The paper integrates gene expression, genetic variants, and clinical data from high-risk Heart Failure patients to identify differentially expressed genes and functionally relevant mutations associated with CVD.