GeoTyper:从原始scRNA-Seq数据到细胞类型识别的自动化管道

C. Wolfe, Yayi Feng, David Chen, E. Purcell, Anne M. Talkington, Sepideh Dolatshahi, Heman Shakeri
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摘要

肿瘤微环境的细胞组成可以直接影响癌症的进展和治疗的效果。了解癌细胞附近的免疫细胞活动,即人体的自然防御机制,对于开发有益的治疗方法至关重要。单细胞RNA测序(scRNA-seq)能够在单个细胞的基础上检查基因表达,提供关于癌症引起的细胞功能紊乱和肿瘤微环境中细胞-细胞通讯的重要信息。这种新技术产生大量的数据,需要适当的处理。有各种工具可以促进这一处理,但需要组织标准化工作流程,从数据整理到可视化、细胞类型识别和细胞活动变化分析,无论是从恶性细胞的角度还是从消除它们的免疫基质细胞的角度。我们的目标是开发一个标准化的管道(GeoTyper, https://github.com/celineyayifeng/GeoTyper),该管道集成了多个scRNA-seq工具,用于处理从NCBI GEO提取的原始序列数据,结果可视化,统计分析和细胞类型鉴定。该管道利用现有的工具,如10X Genomics, Alevin和Seurat的Cellranger,来聚集细胞并根据基因表达谱识别细胞类型。我们成功地在几个公开可用的scRNA-seq数据集上测试和验证了该管道,产生了对应于不同细胞类型的集群。通过确定多种癌症肿瘤微环境中的细胞类型及其各自的频率,该工作流程将有助于量化与细胞-细胞通讯相关的基因表达变化,并确定可能的治疗靶点。
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GeoTyper: Automated Pipeline from Raw scRNA-Seq Data to Cell Type Identification
The cellular composition of the tumor microenvironment can directly impact cancer progression and the efficacy of therapeutics. Understanding immune cell activity, the body's natural defense mechanism, in the vicinity of cancerous cells is essential for developing beneficial treatments. Single cell RNA sequencing (scRNA-seq) enables the examination of gene expression on an individual cell basis, providing crucial information regarding both the disturbances in cell functioning caused by cancer and cell-cell communication in the tumor microenvironment. This novel technique generates large amounts of data, which require proper processing. Various tools exist to facilitate this processing but need to be organized to standardize the workflow from data wrangling to visualization, cell type identification, and analysis of changes in cellular activity, both from the standpoint of malignant cells and immune stromal cells that eliminate them. We aimed to develop a standardized pipeline (GeoTyper, https://github.com/celineyayifeng/GeoTyper) that integrates multiple scRNA-seq tools for processing raw sequence data extracted from NCBI GEO, visualization of results, statistical analysis, and cell type identification. This pipeline leverages existing tools, such as Cellranger from 10X Genomics, Alevin, and Seurat, to cluster cells and identify cell types based on gene expression profiles. We successfully tested and validated the pipeline on several publicly available scRNA-seq datasets, resulting in clusters corresponding to distinct cell types. By determining the cell types and their respective frequencies in the tumor microenvironment across multiple cancers, this workflow will help quantify changes in gene expression related to cell-cell communication and identify possible therapeutic targets.
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