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Dissociation of microdissected mouse brain tissue for artifact free single-cell RNA sequencing

Single-cell RNA sequencing (scRNA-seq) provides the transcriptome of individual cells and addresses previously intractable problems including the central nervous system’s transcriptional responses during health and disease. However, dissociating brain cells is challenging and induces artificial tran...

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Autores principales: Liu, Lu, Besson-Girard, Simon, Ji, Hao, Gehring, Katrin, Bulut, Buket, Kaya, Tuğberk, Usifo, Fumere, Simons, Mikael, Gokce, Ozgun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8196224/
https://www.ncbi.nlm.nih.gov/pubmed/34159323
http://dx.doi.org/10.1016/j.xpro.2021.100590
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author Liu, Lu
Besson-Girard, Simon
Ji, Hao
Gehring, Katrin
Bulut, Buket
Kaya, Tuğberk
Usifo, Fumere
Simons, Mikael
Gokce, Ozgun
author_facet Liu, Lu
Besson-Girard, Simon
Ji, Hao
Gehring, Katrin
Bulut, Buket
Kaya, Tuğberk
Usifo, Fumere
Simons, Mikael
Gokce, Ozgun
author_sort Liu, Lu
collection PubMed
description Single-cell RNA sequencing (scRNA-seq) provides the transcriptome of individual cells and addresses previously intractable problems including the central nervous system’s transcriptional responses during health and disease. However, dissociating brain cells is challenging and induces artificial transcriptional responses. Here, we describe an enzymatic dissociation method for mouse brain that prevents dissociation artifacts and lowers technical variations with standardized steps. We tested this protocol on microdissected brain tissue of 3-week- to 24-month-old mice and obtained high-quality scRNA-seq results. For complete details on the use and execution of this protocol, please refer to Safaiyan et al. (2021).
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spelling pubmed-81962242021-06-21 Dissociation of microdissected mouse brain tissue for artifact free single-cell RNA sequencing Liu, Lu Besson-Girard, Simon Ji, Hao Gehring, Katrin Bulut, Buket Kaya, Tuğberk Usifo, Fumere Simons, Mikael Gokce, Ozgun STAR Protoc Protocol Single-cell RNA sequencing (scRNA-seq) provides the transcriptome of individual cells and addresses previously intractable problems including the central nervous system’s transcriptional responses during health and disease. However, dissociating brain cells is challenging and induces artificial transcriptional responses. Here, we describe an enzymatic dissociation method for mouse brain that prevents dissociation artifacts and lowers technical variations with standardized steps. We tested this protocol on microdissected brain tissue of 3-week- to 24-month-old mice and obtained high-quality scRNA-seq results. For complete details on the use and execution of this protocol, please refer to Safaiyan et al. (2021). Elsevier 2021-06-10 /pmc/articles/PMC8196224/ /pubmed/34159323 http://dx.doi.org/10.1016/j.xpro.2021.100590 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Protocol
Liu, Lu
Besson-Girard, Simon
Ji, Hao
Gehring, Katrin
Bulut, Buket
Kaya, Tuğberk
Usifo, Fumere
Simons, Mikael
Gokce, Ozgun
Dissociation of microdissected mouse brain tissue for artifact free single-cell RNA sequencing
title Dissociation of microdissected mouse brain tissue for artifact free single-cell RNA sequencing
title_full Dissociation of microdissected mouse brain tissue for artifact free single-cell RNA sequencing
title_fullStr Dissociation of microdissected mouse brain tissue for artifact free single-cell RNA sequencing
title_full_unstemmed Dissociation of microdissected mouse brain tissue for artifact free single-cell RNA sequencing
title_short Dissociation of microdissected mouse brain tissue for artifact free single-cell RNA sequencing
title_sort dissociation of microdissected mouse brain tissue for artifact free single-cell rna sequencing
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8196224/
https://www.ncbi.nlm.nih.gov/pubmed/34159323
http://dx.doi.org/10.1016/j.xpro.2021.100590
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