Identification of Spatially Variable Genes (SVGs) Open Access

Ma,Yanru (Spring 2024)

Permanent URL: https://etd.library.emory.edu/concern/etds/td96k399m?locale=en
Published

Abstract

Spatial transcriptomics represents a rapidly evolving technology with profound applications in diverse biological and medical fields. The identification of spatially variable genes (SVGs) is crucial due to the vast number of genes, necessitating selection for tissue-specific relevance, as downstream analyses heavily rely on these chosen SVGs.

Here, we introduce a grid-based approach grounded in the Poisson model, providing a simple yet powerful statistical tool applicable to various spatial transcriptomics datasets. Our method demonstrates adaptability across multiple datasets, exhibiting computational efficiency, especially with high-resolution data.

Our methodology accurately identified all 15 SVGs alongside 85 non-SVGs in each pattern through simulations encompassing prevalent gene spatial patterns including gradients and hotspots. Subsequent validation on three real datasets — both image-based and sequencing-based technologies, conventional and high-resolution platforms — further affirmed the efficacy of our approach. We compared our method to SpatialDE, SPARK-X, and SMASH and identified SVGs bearing biological significance.

Overall, our study underscores the utility and adaptability of our method in advancing spatial transcriptomics research, offering valuable insights into spatial gene expression dynamics.

Table of Contents

1 Introduction

2 Background

2.1 Treedsceek

2.2 SpatialDE

2.3 SPARK and SPARK-X

2.4 Others

3 Methods

3.1 Preprocessing and quality control

3.2 Complete Spatial Randomness

3.3 Poisson Model

4 Results

4.1 Simulations

4.2 Application to Human Osteosarcoma

4.3 Application to Mouse Brain

4.4 Application to Human colon

5 Discussion

A Appendix

Bibliography

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