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

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作者
Natalie Charitakis
Agus Salim
Adam T. Piers
Kevin I. Watt
Enzo R. Porrello
David A. Elliott
Mirana Ramialison
机构
[1] Murdoch Children’s Research Institute,Department of Paediatrics
[2] Royal Children’s Hospital,Novo Nordisk Foundation Center for Stem Cell Medicine
[3] University of Melbourne,Melbourne School of Population and Global Health
[4] Murdoch Children’s Research Institute,School of Mathematics and Statistics
[5] Royal Children’s Hospital,Melbourne Centre for Cardiovascular Genomics and Regenerative Medicine
[6] University of Melbourne,Department of Anatomy and Physiology
[7] University of Melbourne,Department of Diabetes
[8] The Royal Children’s Hospital,undefined
[9] University of Melbourne,undefined
[10] Monash University,undefined
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摘要
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.
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