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Protocol for using single-cell sequencing to study the heterogeneity of NF1 nerve sheath tumors from clinical biospecimens

Single-cell sequencing is a powerful technology to understand the heterogeneity of clinical biospecimens. Here, we present a protocol for obtaining single-cell suspension from neurofibromatosis type 1-associated nerve sheath tumors for transcriptomic profiling on the 10x platform. We describe steps...

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Detalles Bibliográficos
Autores principales: Zhang, Xiyuan, Gopalan, Vishaka, Syed, Neeraja, Hannenhalli, Sridhar, Shern, Jack F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10196853/
https://www.ncbi.nlm.nih.gov/pubmed/37167059
http://dx.doi.org/10.1016/j.xpro.2023.102297
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author Zhang, Xiyuan
Gopalan, Vishaka
Syed, Neeraja
Hannenhalli, Sridhar
Shern, Jack F.
author_facet Zhang, Xiyuan
Gopalan, Vishaka
Syed, Neeraja
Hannenhalli, Sridhar
Shern, Jack F.
author_sort Zhang, Xiyuan
collection PubMed
description Single-cell sequencing is a powerful technology to understand the heterogeneity of clinical biospecimens. Here, we present a protocol for obtaining single-cell suspension from neurofibromatosis type 1-associated nerve sheath tumors for transcriptomic profiling on the 10x platform. We describe steps for clinical sample collection, generation of single-cell suspension, and cell capture and sequencing. We then detail methods for integrative analysis, developmental Schwann cell trajectory building using bioinformatic tools, and comparative analysis. This protocol can be adapted for single-cell sequencing using mouse nerve tumors. For complete details on the use and execution of this protocol, please refer to Zhang et al. (2022).(1)
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spelling pubmed-101968532023-05-20 Protocol for using single-cell sequencing to study the heterogeneity of NF1 nerve sheath tumors from clinical biospecimens Zhang, Xiyuan Gopalan, Vishaka Syed, Neeraja Hannenhalli, Sridhar Shern, Jack F. STAR Protoc Protocol Single-cell sequencing is a powerful technology to understand the heterogeneity of clinical biospecimens. Here, we present a protocol for obtaining single-cell suspension from neurofibromatosis type 1-associated nerve sheath tumors for transcriptomic profiling on the 10x platform. We describe steps for clinical sample collection, generation of single-cell suspension, and cell capture and sequencing. We then detail methods for integrative analysis, developmental Schwann cell trajectory building using bioinformatic tools, and comparative analysis. This protocol can be adapted for single-cell sequencing using mouse nerve tumors. For complete details on the use and execution of this protocol, please refer to Zhang et al. (2022).(1) Elsevier 2023-05-10 /pmc/articles/PMC10196853/ /pubmed/37167059 http://dx.doi.org/10.1016/j.xpro.2023.102297 Text en 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
Zhang, Xiyuan
Gopalan, Vishaka
Syed, Neeraja
Hannenhalli, Sridhar
Shern, Jack F.
Protocol for using single-cell sequencing to study the heterogeneity of NF1 nerve sheath tumors from clinical biospecimens
title Protocol for using single-cell sequencing to study the heterogeneity of NF1 nerve sheath tumors from clinical biospecimens
title_full Protocol for using single-cell sequencing to study the heterogeneity of NF1 nerve sheath tumors from clinical biospecimens
title_fullStr Protocol for using single-cell sequencing to study the heterogeneity of NF1 nerve sheath tumors from clinical biospecimens
title_full_unstemmed Protocol for using single-cell sequencing to study the heterogeneity of NF1 nerve sheath tumors from clinical biospecimens
title_short Protocol for using single-cell sequencing to study the heterogeneity of NF1 nerve sheath tumors from clinical biospecimens
title_sort protocol for using single-cell sequencing to study the heterogeneity of nf1 nerve sheath tumors from clinical biospecimens
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10196853/
https://www.ncbi.nlm.nih.gov/pubmed/37167059
http://dx.doi.org/10.1016/j.xpro.2023.102297
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