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空间变异基因调用中的差异凸显了基准测试空间转录组学方法的必要性。

Disparities in spatially variable gene calling highlight the need for benchmarking spatial transcriptomics methods.

机构信息

Murdoch Children's Research Institute, Royal Children's Hospital, Flemington Road, Parkville, VIC, 3052, Australia.

Department of Paediatrics, University of Melbourne, Grattan Street, Parkville, VIC, 3010, Australia.

出版信息

Genome Biol. 2023 Sep 18;24(1):209. doi: 10.1186/s13059-023-03045-1.

DOI:10.1186/s13059-023-03045-1
PMID:37723583
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10506280/
Abstract

Identifying spatially variable genes (SVGs) is a key step in the analysis of spatially resolved transcriptomics data. SVGs provide biological insights by defining transcriptomic differences within tissues, which was previously unachievable using RNA-sequencing technologies. However, the increasing number of published tools designed to define SVG sets currently lack benchmarking methods to accurately assess performance. This study compares results of 6 purpose-built packages for SVG identification across 9 public and 5 simulated datasets and highlights discrepancies between results. Additional tools for generation of simulated data and development of benchmarking methods are required to improve methods for identifying SVGs.

摘要

鉴定空间可变基因(SVGs)是分析空间分辨转录组学数据的关键步骤。SVGs 通过定义组织内的转录组差异提供了生物学见解,这是以前使用 RNA-seq 技术无法实现的。然而,目前用于定义 SVG 集的已发表工具数量不断增加,但缺乏准确评估性能的基准测试方法。本研究比较了 6 种专门用于 SVG 识别的工具在 9 个公共数据集和 5 个模拟数据集上的结果,并强调了结果之间的差异。需要额外的工具来生成模拟数据和开发基准测试方法,以改进识别 SVGs 的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80cf/10506280/b6c376eaa6f1/13059_2023_3045_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80cf/10506280/9636698403a2/13059_2023_3045_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80cf/10506280/b6c376eaa6f1/13059_2023_3045_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80cf/10506280/9636698403a2/13059_2023_3045_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80cf/10506280/b6c376eaa6f1/13059_2023_3045_Fig2_HTML.jpg

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