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      SCANNER: a web platform for annotation, visualization and sharing of single cell RNA-seq data

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          Abstract

          In recent years, efficient scRNA-seq methods have been developed, enabling the transcriptome profiling of single cells massively in parallel. Meanwhile, its high dimensionality and complexity bring challenges to the data analysis and require extensive collaborations between biologists and bioinformaticians and/or biostatisticians. The communication between these two units demands a platform for easy data sharing and exploration. Here we developed Single-Cell Transcriptomics Annotated Viewer (SCANNER), as a public web resource for the scientific community, for sharing and analyzing scRNA-seq data in a collaborative manner. It is easy-to-use without requiring special software or extensive coding skills. Moreover, it equipped a real-time database for secure data management and enables an efficient investigation of the activation of gene sets on a single-cell basis. Currently, SCANNER hosts a database of 19 types of cancers and COVID-19, as well as healthy samples from lungs of smokers and non-smokers, human brain cells and peripheral blood mononuclear cells (PBMC). The database will be frequently updated with datasets from new studies. Using SCANNER, we identified a larger proportion of cancer-associated fibroblasts cells and more active fibroblast growth-related genes in melanoma tissues in female patients compared to male patients. Moreover, we found ACE2 is mainly expressed in lung pneumocytes, secretory cells and ciliated cells and differentially expressed in lungs of smokers and never smokers.

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          Most cited references16

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          WGCNA: an R package for weighted correlation network analysis

          Background Correlation networks are increasingly being used in bioinformatics applications. For example, weighted gene co-expression network analysis is a systems biology method for describing the correlation patterns among genes across microarray samples. Weighted correlation network analysis (WGCNA) can be used for finding clusters (modules) of highly correlated genes, for summarizing such clusters using the module eigengene or an intramodular hub gene, for relating modules to one another and to external sample traits (using eigengene network methodology), and for calculating module membership measures. Correlation networks facilitate network based gene screening methods that can be used to identify candidate biomarkers or therapeutic targets. These methods have been successfully applied in various biological contexts, e.g. cancer, mouse genetics, yeast genetics, and analysis of brain imaging data. While parts of the correlation network methodology have been described in separate publications, there is a need to provide a user-friendly, comprehensive, and consistent software implementation and an accompanying tutorial. Results The WGCNA R software package is a comprehensive collection of R functions for performing various aspects of weighted correlation network analysis. The package includes functions for network construction, module detection, gene selection, calculations of topological properties, data simulation, visualization, and interfacing with external software. Along with the R package we also present R software tutorials. While the methods development was motivated by gene expression data, the underlying data mining approach can be applied to a variety of different settings. Conclusion The WGCNA package provides R functions for weighted correlation network analysis, e.g. co-expression network analysis of gene expression data. The R package along with its source code and additional material are freely available at .
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            SCANPY : large-scale single-cell gene expression data analysis

            Scanpy is a scalable toolkit for analyzing single-cell gene expression data. It includes methods for preprocessing, visualization, clustering, pseudotime and trajectory inference, differential expression testing, and simulation of gene regulatory networks. Its Python-based implementation efficiently deals with data sets of more than one million cells (https://github.com/theislab/Scanpy). Along with Scanpy, we present AnnData, a generic class for handling annotated data matrices (https://github.com/theislab/anndata).
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              Dissecting the multicellular ecosystem of metastatic melanoma by single-cell RNA-seq.

              To explore the distinct genotypic and phenotypic states of melanoma tumors, we applied single-cell RNA sequencing (RNA-seq) to 4645 single cells isolated from 19 patients, profiling malignant, immune, stromal, and endothelial cells. Malignant cells within the same tumor displayed transcriptional heterogeneity associated with the cell cycle, spatial context, and a drug-resistance program. In particular, all tumors harbored malignant cells from two distinct transcriptional cell states, such that tumors characterized by high levels of the MITF transcription factor also contained cells with low MITF and elevated levels of the AXL kinase. Single-cell analyses suggested distinct tumor microenvironmental patterns, including cell-to-cell interactions. Analysis of tumor-infiltrating T cells revealed exhaustion programs, their connection to T cell activation and clonal expansion, and their variability across patients. Overall, we begin to unravel the cellular ecosystem of tumors and how single-cell genomics offers insights with implications for both targeted and immune therapies.
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                Author and article information

                Contributors
                Journal
                Database (Oxford)
                Database (Oxford)
                databa
                Database: The Journal of Biological Databases and Curation
                Oxford University Press (UK )
                1758-0463
                2022
                17 January 2022
                17 January 2022
                : 2022
                : baab086
                Affiliations
                departmentDepartment of Environmental Health Sciences, Arnold School of Public health, University of South Carolina , Columbia, SC 29208, USA
                departmentDepartment of Epidemiology and Biostatistics, Arnold School of Public Health, University of South Carolina , Columbia, SC 29208, USA
                departmentSan Diego Supercomputer Center, University of California San Diego , La Jolla, CA 92093, USA
                departmentResearch Computing Group, University of South Carolina , Columbia, SC 29208, USA
                departmentDepartment of Epidemiology and Biostatistics, Arnold School of Public Health, University of South Carolina , Columbia, SC 29208, USA
                Author notes
                *Correspondence may also be addressed to Guoshuai Cai. Tel: +803-777-4120; Fax: +803-777-3391; Email: GCAI@ 123456mailbox.sc.edu and Feifei Xiao. Tel: +803-777-8936; Fax: +803-777-2524; Email: xiaof@ 123456mailbox.sc.edu
                Author information
                https://orcid.org/0000-0002-1597-4719
                Article
                baab086
                10.1093/database/baab086
                9246089
                35134150
                56bf05ab-8cea-42fd-8692-9dc730113c8a
                © The Author(s) 2022. Published by Oxford University Press.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 10 August 2021
                : 01 November 2021
                : 27 December 2021
                : 20 December 2021
                : 17 January 2022
                Page count
                Pages: 4
                Funding
                Funded by: UofSC Big Data Health Science Center;
                Award ID: Pilot Study
                Funded by: NSF XSEDE Startup Allocation;
                Award ID: MCB190139
                Categories
                Original Article
                AcademicSubjects/SCI00960

                Bioinformatics & Computational biology
                Bioinformatics & Computational biology

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