SUMMARY: vSPACE is a web-based application presenting a spatial representation of scRNAseq data obtained from human articular cartilage by emulating the concept of spatial transcriptomics technology, but virtually. This virtual 2D plot presentation of human articular cartage cells generates several zonal distribution patterns, for one or multiple genes at a time, revealing patterns that scientists can appreciate as imputed spatial distribution patterns along the zonal axis. AVAILABILITY AND IMPLEMENTATION: vSPACE is implemented in Python Dash as a web-based toolbox designed for data visualization of zonal gene expression patterns in articular cartilage chondrocytes. This tool is freely accessible at: https://vspace.cse.uconn.edu/The source code and extra materials for this service can be downloaded from: https://github.com/zhacheny/vSPACE.

Identifying target genes of a transcription factor is crucial in biomedical research. Thanks to ChIP-seq technology, scientists can estimate potential genome-wide target genes of a transcription factor. However, finding the consistently behaving Up/Down targets of a transcription factor in a given biological context is difficult because it requires analysis of a large number of studies under the same or comparable context. We present a transcription target prediction method, called Cohort-based TF target prediction system (cTAP). This method assumes that the pathway involving the transcription factor of interest is featured with multiple functional groups of marker genes pertaining to the concerned biological process. It uses the notion of gene-presence and gene-absence in addition to log2 ratios of gene expression values for the prediction. Target prediction is made by applying multiple machine-learning models that learn the patterns of genepresence and gene-absence from log2 ratio and four types of Z scores from the normalized cohort's gene expression data. The learned patterns are then associated with the putative targets of the concerned transcription factor to elicit genes exhibiting Up/Down gene regulation patterns “consistently” within the cohort. Totally 11 publicly available GEO data sets related to osteoclastogenesis are used in our experiment. The learned models using gene-presence and gene-absence produce target genes different from using only log2 ratios such as CASP1, BID, and IRF5. Our literature survey reveals that all these predicted targets have known roles in bone remodeling, specifically related to immune and osteoclasts, suggesting confidence in our method and potential merit for a wet-lab experiment for validation.