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Sefer, E.

Publications and source records attributed to Sefer, E..

2 recordsLinked to original sources

Temporal Expression Prediction by Integrating Genome Dynamics via Spatio-temporal GNNs

Temporal gene expression is being analyzed via high-throughput profiling of molecular data over time. The expression values of genes are impacted by their previous expression values as well as the expression of interacting genes over time. Hi-C provides us with a broad genome-wide perspective on the interacting dynamics of genes. In this paper, we propose neural network-based spatio-temporal graph approaches STEPmr and STEPmi to predict changes in mRNA and miRNA expression over time, respectively. Both approaches can integrate a diverse set of Hi-C datasets and features obtained from Hi-C when predicting temporal expression patterns. Our methods can predict mRNA and miRNA expression with 77% and 93% correlation and ith mean squared errors of 0.21 and 0.01, explaining 59.1% and 88% of the variance, respectively. Important characteristics of the genes with the highest performances in both datasets are that they are structural signaling genes or transcriptional regulators involved in fundamental processes such as homeostasis, development, and RNA processing. Additionally, they are not limited to a specific cell type, but rather show constant expression throughout different tissues. In contrast, the lowest-performed genes generally behave in context-dependent expression patterns, where they include condition-specific biological functions instead of vital biological activities. These findings suggest a model of gene regulation and its predictability that is impacted by interacting gene dynamics. Our code and datasets are publicly available at https://github.com/seferlab/temporalhic.

bioinformatics↗

GAT-HiC: Efficient Reconstruction of 3D Chromosome Structure via Residual Graph Attention Neural Networks

Hi-C is an experimental technique to measure the genome-wide topological dynamics and three-dimensional (3D) shape of chromosomes indirectly via counting the number of interactions between distinct sets of loci. One can estimate the 3D shape of a chromosome over these indirect interaction datasets. Here, we come up with graph attention and residual network-based GAT-HiC to predict three-dimensional chromosome structure from Hi-C interactions. GAT-HiC is distinct from the existing 3D chromosome shape prediction approaches in a way that it can generalize to data that is different than train data. So, we can train GAT-HiC on one type of Hi-C interaction matrix and infer on a completely dissimilar interaction matrix. GAT-HiC combines the unsupervised vertex embedding method Node2vec with an attention-based graph neural network when predicting each genomic locis three-dimensional coordinates from Hi-C interaction matrix. We test the performance of our method across multiple Hi-C interaction datasets, where a trained model can be generalized across distinct cell populations, distinct restriction enzymes, and distinct Hi-C resolutions over human and mouse. GAT-HiC can reconstruct accurately in all these scenarios. Our method outperforms the existing approaches in terms of the accuracy of three-dimensional chromosome shape inference over interaction datasets. Code and datasets can be found at https://github.com/beyzoskaya/GAT-HiC.

bioinformatics↗