标杆管理
水准点(测量)
聚类分析
转录组
DNA微阵列
计算生物学
计算机科学
分割
模式识别(心理学)
数据挖掘
生物信息学
人工智能
生物
地图学
业务
地理
遗传学
基因
基因表达
营销
作者
Huan Wang,Ruixu Huang,Jack Nelson,Ce Gao,Miles Tran,Anna Yeaton,Kristen D. Felt,Kathleen L. Pfaff,Teri Bowman,Scott J. Rodig,Kevin Wei,Brittany A. Goods,Samouil L. Farhi
出处
期刊:
[Cold Spring Harbor Laboratory]
日期:2023-12-08
被引量:79
标识
DOI:10.1101/2023.12.07.570603
摘要
Emerging imaging spatial transcriptomics (iST) platforms and coupled analytical methods can recover cell-to-cell interactions, groups of spatially covarying genes, and gene signatures associated with pathological features, and are thus particularly well-suited for applications in formalin fixed paraffin embedded (FFPE) tissues. Here, we benchmarked the performance of three commercial iST platforms on serial sections from tissue microarrays (TMAs) containing 23 tumor and normal tissue types for both relative technical and biological performance. On matched genes, we found that 10x Xenium shows higher transcript counts per gene without sacrificing specificity, but that all three platforms concord to orthogonal RNA-seq datasets and can perform spatially resolved cell typing, albeit with different false discovery rates, cell segmentation error frequencies, and with varying degrees of sub-clustering for downstream biological analyses. Taken together, our analyses provide a comprehensive benchmark to guide the choice of iST method as researchers design studies with precious samples in this rapidly evolving field.
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