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Gene panel selection for targeted spatial transcriptomics

Targeted spatial transcriptomics hold particular promise in analysis of complex tissues. Most such methods, however, measure only a limited panel of transcripts, which need to be selected in advance to inform on the cell types or processes being studied. A limitation of existing gene selection metho...

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Autores principales: Zhang, Yida, Petukhov, Viktor, Biederstedt, Evan, Que, Richard, Zhang, Kun, Kharchenko, Peter V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10054990/
https://www.ncbi.nlm.nih.gov/pubmed/36993340
http://dx.doi.org/10.1101/2023.02.03.527053
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author Zhang, Yida
Petukhov, Viktor
Biederstedt, Evan
Que, Richard
Zhang, Kun
Kharchenko, Peter V.
author_facet Zhang, Yida
Petukhov, Viktor
Biederstedt, Evan
Que, Richard
Zhang, Kun
Kharchenko, Peter V.
author_sort Zhang, Yida
collection PubMed
description Targeted spatial transcriptomics hold particular promise in analysis of complex tissues. Most such methods, however, measure only a limited panel of transcripts, which need to be selected in advance to inform on the cell types or processes being studied. A limitation of existing gene selection methods is that they rely on scRNA-seq data, ignoring platform effects between technologies. Here we describe gpsFISH, a computational method to perform gene selection through optimizing detection of known cell types. By modeling and adjusting for platform effects, gpsFISH outperforms other methods. Furthermore, gpsFISH can incorporate cell type hierarchies and custom gene preferences to accommodate diverse design requirements.
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spelling pubmed-100549902023-03-30 Gene panel selection for targeted spatial transcriptomics Zhang, Yida Petukhov, Viktor Biederstedt, Evan Que, Richard Zhang, Kun Kharchenko, Peter V. bioRxiv Article Targeted spatial transcriptomics hold particular promise in analysis of complex tissues. Most such methods, however, measure only a limited panel of transcripts, which need to be selected in advance to inform on the cell types or processes being studied. A limitation of existing gene selection methods is that they rely on scRNA-seq data, ignoring platform effects between technologies. Here we describe gpsFISH, a computational method to perform gene selection through optimizing detection of known cell types. By modeling and adjusting for platform effects, gpsFISH outperforms other methods. Furthermore, gpsFISH can incorporate cell type hierarchies and custom gene preferences to accommodate diverse design requirements. Cold Spring Harbor Laboratory 2023-03-24 /pmc/articles/PMC10054990/ /pubmed/36993340 http://dx.doi.org/10.1101/2023.02.03.527053 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator.
spellingShingle Article
Zhang, Yida
Petukhov, Viktor
Biederstedt, Evan
Que, Richard
Zhang, Kun
Kharchenko, Peter V.
Gene panel selection for targeted spatial transcriptomics
title Gene panel selection for targeted spatial transcriptomics
title_full Gene panel selection for targeted spatial transcriptomics
title_fullStr Gene panel selection for targeted spatial transcriptomics
title_full_unstemmed Gene panel selection for targeted spatial transcriptomics
title_short Gene panel selection for targeted spatial transcriptomics
title_sort gene panel selection for targeted spatial transcriptomics
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10054990/
https://www.ncbi.nlm.nih.gov/pubmed/36993340
http://dx.doi.org/10.1101/2023.02.03.527053
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