Shui, Lan, Maitra, Anirban, Yuan, Ying, Lau, Ken S., Kaur, Harsimran, Li, Liang, & Li, Ziyi. (2025). “.� PLOS Computational Biology, 21(7), e1013293.
Recent advances inÌýspatial transcriptomics (ST)—a technique that measures gene activity in tissue while preserving its location—have greatly improved biological research. However, current ST methods are expensive, making large-scale studies difficult. This creates a need toÌýmake the most of available dataÌýto achieve reliable results.
A key task in ST research is identifyingÌýgenes that behave differently under different conditions, known asÌýdifferentially expressed genes (DEGs). While these analyses are common, how to calculate theirÌýstatistical power—the ability to detect real differences—is rarely discussed.
To address this, we developedÌýPoweREST, a tool that estimates the power of DEG detection usingÌý10X Genomics Visium data. PoweREST can be usedÌýbefore starting experimentsÌýorÌýafter collecting preliminary data, making it flexible for many study designs. We also created aÌýuser-friendly web applicationthat allows researchers to easily calculate and visualize the power of their ST studies without needing to write any code.

Fig 1. Schema of the proposed PoweREST method.
When a preliminary cohort of ST data is available, PoweREST performs the power calculation based on bootstrap and P-splines fitting. When preliminary data are not available, an R Shiny app with power estimation results based on datasets from two cancer studies can be used. Created in BioRender. Shui, L. (2025)