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Abstract Differential expression is a key application of imaging spatial transcriptomics, moving analysis beyond cell type localization to examining cell state responses to microenvironments. However, spatial data poses new challenges to differential expression: segmentation errors cause bias in fold-change estimates, and correlation among neighboring cells leads standard models to inflate statistical significance. We find that ignoring these issues can result in considerable false discoveries that greatly outnumber true findings. We present a suite of solutions to these fundamental challenges, and implement them in the R package smiDE. spatial transcriptomics, differential expression, segmentation error mitigation, spatial correlation, spatial random effects model
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Ana Gabriela Vasconcelos
Daniel McGuire
Bruker (United States)
Noah Simon
University of Washington
University of Washington
Nanostring Technologies (United States)
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Vasconcelos et al. (Tue,) studied this question.
synapsesocial.com/papers/68e5d358b6db643587569e5e — DOI: https://doi.org/10.1101/2024.08.02.606405