Publication Date
2-26-2024
Journal
Genome Biology
DOI
10.1186/s13059-024-03185-y
PMID
38408997
PMCID
PMC10895727
PubMedCentral® Posted Date
2-26-2024
PubMedCentral® Full Text Version
Post-print
Published Open-Access
yes
Keywords
In Situ Hybridization, Fluorescence, Gene Expression Profiling, Transcriptome
Abstract
A critical challenge of single-cell spatial transcriptomics (sc-ST) technologies is their panel size. Being based on fluorescence in situ hybridization, they are typically limited to panels of about a thousand genes. This constrains researchers to build panels from only the marker genes of different cell types and forgo other genes of interest, e.g., genes encoding ligand-receptor complexes or those in specific pathways. We propose scGIST, a constrained feature selection tool that designs sc-ST panels prioritizing user-specified genes without compromising cell type detection accuracy. We demonstrate scGIST's efficacy in diverse use cases, highlighting it as a valuable addition to sc-ST's algorithmic toolbox.
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