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Genome Biol ; 25(1): 57, 2024 Feb 26.
Artigo em Inglês | MEDLINE | ID: mdl-38408997

RESUMO

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.


Assuntos
Perfilação da Expressão Gênica , Transcriptoma , Hibridização in Situ Fluorescente
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