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GeoTyper: Automated Pipeline from Raw scRNA-Seq Data to Cell Type Identification

  • Cecily Wolfe
  • , Yayi Feng
  • , David Chen
  • , Edwin Purcell
  • , Anne Talkington
  • , Sepideh Dolatshahi
  • , Heman Shakeri
  • University of Virginia

Research output: Chapter in Book/Report/Conference proceedingConference contributionpeer-review

1 Scopus citations

Abstract

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.

Original languageEnglish
Title of host publication2022 Systems and Information Engineering Design Symposium, SIEDS 2022
PublisherInstitute of Electrical and Electronics Engineers Inc.
Pages223-228
Number of pages6
ISBN (Electronic)9781665451116
DOIs
StatePublished - 2022
Event2022 Systems and Information Engineering Design Symposium, SIEDS 2022 - Charlottesville, United States
Duration: Apr 28 2022Apr 29 2022

Publication series

Name2022 Systems and Information Engineering Design Symposium, SIEDS 2022

Conference

Conference2022 Systems and Information Engineering Design Symposium, SIEDS 2022
Country/TerritoryUnited States
CityCharlottesville
Period04/28/2204/29/22

Keywords

  • Cancer
  • Cell Type Identification
  • NCBI GEO
  • Pipeline
  • Seurat
  • scRNA-Seq

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