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Calogero, R.

Publications and source records attributed to Calogero, R..

3 recordsLinked to original sources

Stardust: improving spatial transcriptomics data analysis through space aware modularity optimization based clustering.

BackgroundSpatial transcriptomics (ST) combines stained tissue images with spatially resolved high-throughput RNA sequencing. The spatial transcriptomic analysis includes challenging tasks like clustering, where a partition among data points (spots) is defined by means of a similarity measure. Improving clustering results is a key factor as clustering affects subsequent downstream analysis. State-of-the-art approaches group data by taking into account transcriptional similarity and some by exploiting spatial information as well. However, it is not yet clear how much the spatial information combined with transcriptomics improves the clustering result. ResultsWe propose a new clustering method, Stardust, that easily exploits the combination of space and transcriptomic information in the clustering procedure through a manual or fully automatic tuning of algorithm parameters. Moreover, a parameter-free version of the method is also provided where the spatial contribution depends dynamically on the expression distances distribution in the space. We evaluated the proposed methods results by analysing ST datasets available on the 10x Genomics website and comparing clustering performances with state-of-the-art approaches by measuring the spots stability in the clusters and their biological coherence. Stability is defined by the tendency of each point to remain clustered with the same neighbours when perturbations are applied. ConclusionsStardust is an easy-to-use methodology allowing to define how much spatial information should influence clustering on different tissues and achieving more stable results than state-of-the-art approaches.

bioinformatics↗

Sparsely-Connected Autoencoder (SCA) for single cell RNAseq data mining

Single-cell RNA sequencing (scRNAseq) is an essential tool to investigate cellular heterogeneity. Although scRNAseq has some technical challenges, it would be of great interest being able to disclose biological information out of cell subpopulations, which can be defined by cluster analysis of scRNAseq data. In this manuscript, we evaluated the efficacy of sparsely-connected autoencoder (SCA) as tool for the functional mining of single cells clusters. We show that SCA can be uses as tool to uncover hidden features associated to scRNAseq data. Our approach is strengthened by two metrics, QCF and QCM, which respectively allow to evaluate the ability of SCA to reconstruct a cells cluster and to evaluate the overall quality of the neural network model. Our data indicate that SCA encoded spaces, derived by different experimentally validated data (TFs targets, miRNAs targets, Kinases targets, and cancer-related immune signatures), can be used to grasp single cell cluster-specific functional features. In our implementation, SCA efficacy comes from its ability to reconstruct only specific clusters, thus indicating only those clusters where the SCA encoding space is a key element for cells aggregation. SCA analysis is implemented as module in rCASC framework and it is supported by a GUI to simplify it usage for biologists and medical personnel.

bioinformatics↗

rCASC: reproducible Classification Analysis of Single Cell sequencing data

SummarySingle-cell RNA sequencing has emerged as an essential tool to investigate cellular heterogeneity, and highlighting cell sub-population specific signatures. Nowadays, dedicated and user-friendly bioinformatics workflows are required to exploit the deconvolution of single-cells transcriptome. Furthermore, there is a growing need of bioinformatics workflows granting both functional, i.e. saving information about data and analysis parameters, and computation reproducibility, i.e. storing the real image of the computation environment. Here, we present rCASC a modular RNAseq analysis workflow allowing data analysis from counts generation to cell sub-population signatures identification, granting both functional and computation reproducibility.\n\nAvailability and ImplementationrCASC is part of the reproducible bioinfomatics project. rCASC is a docker based application controlled by a R package available at https://github.com/kendomaniac/rCASC.\n\nSupplementary informationSupplementary data are available at rCASC github

bioinformatics↗