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Biology subjects

Gora, S.

Publications and source records attributed to Gora, S..

2 recordsLinked to original sources

A Robust and Interpretable Feature Engineering Approach for Low-Data Biological Classification

Accurate biological classification often faces challenges from high-dimensional data and limited samples, leading to model overfitting and poor interpretability. This study introduces Directional Flow Embedding (DFE), a novel feature engineering and embedding method designed to overcome these issues. DFE transforms raw biological data into three concise and biologically interpretable features: Directional Flow Score (DFS), Heterogeneity Index (HI), and Local Density Estimate (LDE). It achieves this by robustly determining a global direction vector from class means, enabling the projection of samples onto this principal axis, quantifying their deviation, and incorporating local density information. Evaluated on real-world TCGA-BRCA and TCGA-LUAD RNA-sequencing datasets, DFE consistently demonstrated superior performance. It significantly outperformed traditional methods and strong non-linear models. Ablation studies confirmed the synergistic contribution of all three DFE features, while sensitivity analysis revealed its robustness. DFEs inherent interpretability, strong generalizability, and computational efficiency make it a valuable tool for robust and transparent biological classification, thereby advancing critical applications in biomedical research and clinical decision-making.

bioinformatics↗

A novel interaction between Gβγ and RNA polymerase II regulates cardiac fibrosis.

G{beta}{gamma} subunits are involved in many different signalling processes in various compartments of the cell, including the nucleus. To gain insight into the functions of nuclear G{beta}{gamma}, we investigated the functional role of G{beta}{gamma} signalling in regulation of GPCR-mediated gene expression in primary rat neonatal cardiac fibroblasts. Following activation of the angiotensin II type I receptor in these cells, G{beta}{gamma} dimers interact with RNA polymerase II (RNAPII). Our findings suggest that G{beta}1 recruitment to RNAPII negatively regulates the fibrotic transcriptional response, which can be overcome by strong fibrotic stimuli. The interaction between G{beta}{gamma} subunits and RNAPII expands the role for G{beta}{gamma} signalling in cardiac fibrosis. The G{beta}{gamma}-RNAPII interaction was regulated by signaling pathways in HEK 293 cells that diverged from those operating in cardiac fibroblasts. Thus, the interaction may be a conserved feature of transcriptional regulation although such regulation may be cell-specific.

biochemistry↗