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Zandavi, S. M.

Publications and source records attributed to Zandavi, S. M..

2 recordsLinked to original sources

Omics Imagification: Transforming High-throughput Molecular Representation of a Cell into an Image

Different omics profiles, depending on the underlying technology, encompass measurements of several hundred to several thousand molecules in a biological sample or a cell. This study develops upon the concept of "omics imagification" as a process of transforming a vector representing these numerical measurements into an image with a one-to-one relationship with the corresponding sample. The proposed imagification process transforms a high-dimensional vector of molecular measurements into a two-dimensional RGB image to enable holistic molecular representation of a biological sample and to improve the classification of different biological phenotypes using automated image recognition methods in computer vision. A transformed image represents 2D coordinates of molecules in a neighbour-embedded space representing molecular abundance and gene intensity. The proposed method was applied to a single-cell RNA sequencing (scRNA-seq) data to "imagify" gene expression profiles of individual cells. Our results show that a simple convolutional neural network trained on single-cell transcriptomics images accurately classifies diverse cell types outperforming the best-performing scRNA-seq classifiers such as support vector machine and random forest.

bioinformatics↗

Disentangling single-cell omics representation with a power spectral density-based feature extraction

Emerging single-cell technologies provide high-resolution measurements of distinct cellular modalities opening new avenues for generating detailed cellular atlases of many and diverse tissues. The high dimensionality, sparsity, and inaccuracy of single cell sequencing measurements, however, can obscure discriminatory information, mask cellular subtype variations and complicate downstream analyses which can limit our understanding of cell function and tissue heterogeneity. Here, we present a novel pre-processing method (scPSD) inspired by power spectral density analysis that enhances the accuracy for cell subtype separation from large-scale single-cell omics data. We comprehensively benchmarked our method on a wide range of single-cell RNA-sequencing datasets and showed that scPSD pre-processing, while being fast and scalable, significantly reduces data complexity, enhances cell-type separation, and enables rare cell identification. Additionally, we applied scPSD to transcriptomics and chromatin accessibility cell atlases and demonstrated its capacity to discriminate over 100 cell types across the whole organism and across different modalities of single-cell omics data.

bioinformatics↗