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A protocol for simultaneous high-sensitivity genotyping and chromatin accessibility profiling in single cells

Single-cell assay for transposase-accessible chromatin with sequencing (scATAC-seq) resolves the heterogeneity of epigenetic states across cells but does not typically capture exonic mutations, which limits our knowledge of how somatic mutations alter chromatin landscapes. Here, we present a plate-b...

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Autores principales: Turkalj, Sven, Jakobsen, Niels Asger, Groom, Angus, Radtke, Felix A., Vyas, Paresh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10641301/
https://www.ncbi.nlm.nih.gov/pubmed/37897733
http://dx.doi.org/10.1016/j.xpro.2023.102641
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author Turkalj, Sven
Jakobsen, Niels Asger
Groom, Angus
Radtke, Felix A.
Vyas, Paresh
author_facet Turkalj, Sven
Jakobsen, Niels Asger
Groom, Angus
Radtke, Felix A.
Vyas, Paresh
author_sort Turkalj, Sven
collection PubMed
description Single-cell assay for transposase-accessible chromatin with sequencing (scATAC-seq) resolves the heterogeneity of epigenetic states across cells but does not typically capture exonic mutations, which limits our knowledge of how somatic mutations alter chromatin landscapes. Here, we present a plate-based approach coupling high-sensitivity genotyping of genomic loci with high-content scATAC-seq libraries from the same single cells. We first describe steps for optimization of genotyping primers, followed by detailed guidance on the preparation of both scATAC-seq and single-cell genotyping libraries, fully automated on high-throughput liquid handling platforms. For complete details on the use and execution of this protocol, please refer to Turkalj, Jakobsen et al.(1)
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spelling pubmed-106413012023-11-14 A protocol for simultaneous high-sensitivity genotyping and chromatin accessibility profiling in single cells Turkalj, Sven Jakobsen, Niels Asger Groom, Angus Radtke, Felix A. Vyas, Paresh STAR Protoc Protocol Single-cell assay for transposase-accessible chromatin with sequencing (scATAC-seq) resolves the heterogeneity of epigenetic states across cells but does not typically capture exonic mutations, which limits our knowledge of how somatic mutations alter chromatin landscapes. Here, we present a plate-based approach coupling high-sensitivity genotyping of genomic loci with high-content scATAC-seq libraries from the same single cells. We first describe steps for optimization of genotyping primers, followed by detailed guidance on the preparation of both scATAC-seq and single-cell genotyping libraries, fully automated on high-throughput liquid handling platforms. For complete details on the use and execution of this protocol, please refer to Turkalj, Jakobsen et al.(1) Elsevier 2023-10-26 /pmc/articles/PMC10641301/ /pubmed/37897733 http://dx.doi.org/10.1016/j.xpro.2023.102641 Text en Crown Copyright © 2023. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Protocol
Turkalj, Sven
Jakobsen, Niels Asger
Groom, Angus
Radtke, Felix A.
Vyas, Paresh
A protocol for simultaneous high-sensitivity genotyping and chromatin accessibility profiling in single cells
title A protocol for simultaneous high-sensitivity genotyping and chromatin accessibility profiling in single cells
title_full A protocol for simultaneous high-sensitivity genotyping and chromatin accessibility profiling in single cells
title_fullStr A protocol for simultaneous high-sensitivity genotyping and chromatin accessibility profiling in single cells
title_full_unstemmed A protocol for simultaneous high-sensitivity genotyping and chromatin accessibility profiling in single cells
title_short A protocol for simultaneous high-sensitivity genotyping and chromatin accessibility profiling in single cells
title_sort protocol for simultaneous high-sensitivity genotyping and chromatin accessibility profiling in single cells
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10641301/
https://www.ncbi.nlm.nih.gov/pubmed/37897733
http://dx.doi.org/10.1016/j.xpro.2023.102641
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