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Rifat, J. I. M.

Publications and source records attributed to Rifat, J. I. M..

2 recordsLinked to original sources

MultiGEOmics: Graph-Based Integration of Multi-Omics via Biological Information Flows

Multi-omics datasets capture complementary aspects of biological systems and are central to modern machine learning applications in biology and medicine. Existing graph-based integration methods typically construct separate graphs for each omics type and focus primarily on intra-omic relationships. As a result, they often overlook cross-omics regulatory signals--bidirectional interactions across omics layers--that are critical for modeling complex cellular processes. A second major challenge is missing or incomplete omics data; many current approaches degrade substantially in performance or exclude patients lacking one or more omics modalities. To address these limitations, we introduce MultiGEOmics, an intermediate-level graph integration framework that explicitly incorporates regulatory signals across omics types during graph representation learning and models biologically inspired omics-specific and cross-omics dependencies. MultiGEOmics learns robust cross-omics embeddings that remain reliable even when some modalities are partially missing. We evaluated MultiGEOmics across eleven datasets spanning cancer and Alzheimers disease, under zero, moderate, and high missing-rate scenarios. MultiGEOmics consistently maintains strong predictive performance across all missing-data conditions while offering interpretability by identifying the most influential omics types and features for each prediction task. The source code and the documentation of MultiGEOmics are available at https://github.com/bozdaglab/MultiGEOmics.

bioinformatics↗

scAURA: Alignment- and Uniformity-based Graph DebiasedContrastive Representation Architecture for Self-SupervisedClustering of Single-Cell Transcriptomics

Single-cell RNA sequencing (scRNA-seq) allows transcriptomic profiling at single-cell resolution, providing valuable insights into cellular diversity across tissues, developmental stages, and diseases. However, accurately identifying cell types remains challenging due to the high dimensionality, sparsity, and noise inherent in scRNA-seq data. To address these challenges in cell type identification in scRNA-seq data, we introduce scAURA (single cell Alignment- and Uniformity-based Graph Debiased Contrastive Representation Architecture), a unified framework that integrates graph debiased contrastive learning with self-supervised clustering. We evaluated scAURA on 18 real single-cell datasets collected from six sequencing platforms spanning diverse tissue and cell types in human and mouse. scAURA outperformed all state-of-the-art (SOTA) methods in nine and eight datasets in Adjusted Rand Index (ARI) and Normalized Mutual Information (NMI), respectively. On average, scAURA obtained average ranks of 2.28 (ARI) and 2.39 (NMI) across all 13 SOTA methods, demonstrating its consistent superiority across datasets. scAURA also exhibited strong robustness to dropout noise by maintaining stable clustering performance even under increasing sparsity levels. Furthermore, in an external single-cell Alzheimers disease dataset, scAURA accurately clustered different cell types, identified novel cell type-specific marker genes, and inferred their potential transcriptional regulators. The source code and datasets are available at https://github.com/bozdaglab/scAURA. ContactSerdar.Bozdag@unt.edu

bioinformatics↗