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HybriSeq: Probe-based Device-free Single-cell RNA Profiling
We have developed the HybriSeq method for single-cell RNA profiling, which utilizes in situ hybridization of multiple probes for targeted transcripts, followed by split-pool barcoding and sequencing analysis of the probes. We have shown that HybriSeq can achieve high sensitivity for RNA detection wi...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10557710/ https://www.ncbi.nlm.nih.gov/pubmed/37808850 http://dx.doi.org/10.1101/2023.09.27.559406 |
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author | Foyt, Daniel Brown, David Zhou, Shuqin Huang, Bo |
author_facet | Foyt, Daniel Brown, David Zhou, Shuqin Huang, Bo |
author_sort | Foyt, Daniel |
collection | PubMed |
description | We have developed the HybriSeq method for single-cell RNA profiling, which utilizes in situ hybridization of multiple probes for targeted transcripts, followed by split-pool barcoding and sequencing analysis of the probes. We have shown that HybriSeq can achieve high sensitivity for RNA detection with multiple probes and profile RNA accessibility. The utility of HybriSeq is demonstrated in characterizing cell-to-cell heterogeneities of a panel of 95 cell-cycle-related genes and the probe-probe heterogeneity within a single transcript. |
format | Online Article Text |
id | pubmed-10557710 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-105577102023-10-07 HybriSeq: Probe-based Device-free Single-cell RNA Profiling Foyt, Daniel Brown, David Zhou, Shuqin Huang, Bo bioRxiv Article We have developed the HybriSeq method for single-cell RNA profiling, which utilizes in situ hybridization of multiple probes for targeted transcripts, followed by split-pool barcoding and sequencing analysis of the probes. We have shown that HybriSeq can achieve high sensitivity for RNA detection with multiple probes and profile RNA accessibility. The utility of HybriSeq is demonstrated in characterizing cell-to-cell heterogeneities of a panel of 95 cell-cycle-related genes and the probe-probe heterogeneity within a single transcript. Cold Spring Harbor Laboratory 2023-09-29 /pmc/articles/PMC10557710/ /pubmed/37808850 http://dx.doi.org/10.1101/2023.09.27.559406 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 Foyt, Daniel Brown, David Zhou, Shuqin Huang, Bo HybriSeq: Probe-based Device-free Single-cell RNA Profiling |
title | HybriSeq: Probe-based Device-free Single-cell RNA Profiling |
title_full | HybriSeq: Probe-based Device-free Single-cell RNA Profiling |
title_fullStr | HybriSeq: Probe-based Device-free Single-cell RNA Profiling |
title_full_unstemmed | HybriSeq: Probe-based Device-free Single-cell RNA Profiling |
title_short | HybriSeq: Probe-based Device-free Single-cell RNA Profiling |
title_sort | hybriseq: probe-based device-free single-cell rna profiling |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10557710/ https://www.ncbi.nlm.nih.gov/pubmed/37808850 http://dx.doi.org/10.1101/2023.09.27.559406 |
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