Shui, Lan, Maitra, Anirban, Yuan, Ying, Lau, Ken S., Kaur, Harsimran, Li, Liang, & Li, Ziyi. (2025). “.” PLOS Computational Biology, 21(7), e1013293.
Recent advances inspatial 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 tomake the most of available datato achieve reliable results.
A key task in ST research is identifyinggenes that behave differently under different conditions, known asdifferentially expressed genes (DEGs). While these analyses are common, how to calculate theirstatistical power—the ability to detect real differences—is rarely discussed.
To address this, we developedPoweREST, a tool that estimates the power of DEG detection using10X Genomics Visium data. PoweREST can be usedbefore starting experimentsorafter collecting preliminary data, making it flexible for many study designs. We also created auser-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)