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Detection of differentially expressed genes in spatial transcriptomics data by spatial analysis of spatial transcriptomics: A novel method based on spatial statistics

BACKGROUND: Spatial transcriptomics (STs) simultaneously obtains the location and amount of gene expression within a tissue section. However, current methods like FindMarkers calculated the differentially expressed genes (DEGs) based on the classical statistics, which should abolish the spatial info...

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Autores principales: Qiu, Zhihua, Li, Shaojun, Luo, Ming, Zhu, Shuanggen, Wang, Zhijian, Jiang, Yongjun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9745188/
https://www.ncbi.nlm.nih.gov/pubmed/36523429
http://dx.doi.org/10.3389/fnins.2022.1086168
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author Qiu, Zhihua
Li, Shaojun
Luo, Ming
Zhu, Shuanggen
Wang, Zhijian
Jiang, Yongjun
author_facet Qiu, Zhihua
Li, Shaojun
Luo, Ming
Zhu, Shuanggen
Wang, Zhijian
Jiang, Yongjun
author_sort Qiu, Zhihua
collection PubMed
description BACKGROUND: Spatial transcriptomics (STs) simultaneously obtains the location and amount of gene expression within a tissue section. However, current methods like FindMarkers calculated the differentially expressed genes (DEGs) based on the classical statistics, which should abolish the spatial information. MATERIALS AND METHODS: A new method named spatial analysis of spatial transcriptomics (saSpatial) was developed for both the location and the amount of gene expression. Then saSpatial was applied to detect DEGs in both inter- and intra-cross sections. DEGs detected by saSpatial were compared with those detected by FindMarkers. RESULTS: Spatial analysis of spatial transcriptomics was founded on the basis of spatial statistics. It was able to detect DEGs in different regions in the normal brain section. As for the brain with ischemic stroke, saSpatial revealed the DEGs for the ischemic core and penumbra. In addition, saSpatial characterized the genetic heterogeneity in the normal and ischemic cortex. Compared to FindMarkers, a larger number of valuable DEGs were found by saSpatial. CONCLUSION: Spatial analysis of spatial transcriptomics was able to effectively detect DEGs in STs data. It was a simple and valuable tool that could help potential researchers to find more valuable genes in the future research.
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spelling pubmed-97451882022-12-14 Detection of differentially expressed genes in spatial transcriptomics data by spatial analysis of spatial transcriptomics: A novel method based on spatial statistics Qiu, Zhihua Li, Shaojun Luo, Ming Zhu, Shuanggen Wang, Zhijian Jiang, Yongjun Front Neurosci Neuroscience BACKGROUND: Spatial transcriptomics (STs) simultaneously obtains the location and amount of gene expression within a tissue section. However, current methods like FindMarkers calculated the differentially expressed genes (DEGs) based on the classical statistics, which should abolish the spatial information. MATERIALS AND METHODS: A new method named spatial analysis of spatial transcriptomics (saSpatial) was developed for both the location and the amount of gene expression. Then saSpatial was applied to detect DEGs in both inter- and intra-cross sections. DEGs detected by saSpatial were compared with those detected by FindMarkers. RESULTS: Spatial analysis of spatial transcriptomics was founded on the basis of spatial statistics. It was able to detect DEGs in different regions in the normal brain section. As for the brain with ischemic stroke, saSpatial revealed the DEGs for the ischemic core and penumbra. In addition, saSpatial characterized the genetic heterogeneity in the normal and ischemic cortex. Compared to FindMarkers, a larger number of valuable DEGs were found by saSpatial. CONCLUSION: Spatial analysis of spatial transcriptomics was able to effectively detect DEGs in STs data. It was a simple and valuable tool that could help potential researchers to find more valuable genes in the future research. Frontiers Media S.A. 2022-11-29 /pmc/articles/PMC9745188/ /pubmed/36523429 http://dx.doi.org/10.3389/fnins.2022.1086168 Text en Copyright © 2022 Qiu, Li, Luo, Zhu, Wang and Jiang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Qiu, Zhihua
Li, Shaojun
Luo, Ming
Zhu, Shuanggen
Wang, Zhijian
Jiang, Yongjun
Detection of differentially expressed genes in spatial transcriptomics data by spatial analysis of spatial transcriptomics: A novel method based on spatial statistics
title Detection of differentially expressed genes in spatial transcriptomics data by spatial analysis of spatial transcriptomics: A novel method based on spatial statistics
title_full Detection of differentially expressed genes in spatial transcriptomics data by spatial analysis of spatial transcriptomics: A novel method based on spatial statistics
title_fullStr Detection of differentially expressed genes in spatial transcriptomics data by spatial analysis of spatial transcriptomics: A novel method based on spatial statistics
title_full_unstemmed Detection of differentially expressed genes in spatial transcriptomics data by spatial analysis of spatial transcriptomics: A novel method based on spatial statistics
title_short Detection of differentially expressed genes in spatial transcriptomics data by spatial analysis of spatial transcriptomics: A novel method based on spatial statistics
title_sort detection of differentially expressed genes in spatial transcriptomics data by spatial analysis of spatial transcriptomics: a novel method based on spatial statistics
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9745188/
https://www.ncbi.nlm.nih.gov/pubmed/36523429
http://dx.doi.org/10.3389/fnins.2022.1086168
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