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

Abstract:

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

Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1016/j.xpro.2023.102641

Authors


More by this author
Institution:
University of Oxford
Division:
MSD
Department:
RDM
Sub department:
Weatherall Insti. of Molecular Medicine
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
RDM
Sub department:
RDM Clinical Laboratory Sciences
Research group:
Weatherall Insti. of Molecular Medicine
Role:
Author
ORCID:
0000-0002-5776-5085
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
RDM
Sub department:
Weatherall Insti. of Molecular Medicine
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
RDM
Sub department:
Weatherall Insti. of Molecular Medicine
Oxford college:
Green Templeton College
Role:
Author
ORCID:
0000-0002-6491-2573
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
RDM
Sub department:
Weatherall Insti. of Molecular Medicine
Oxford college:
St Anne's College
Role:
Author
ORCID:
0000-0003-3931-0914


Publisher:
Cell Press
Journal:
STAR Protocols More from this journal
Volume:
4
Issue:
4
Article number:
102641
Place of publication:
United States
Publication date:
2023-10-26
Acceptance date:
2023-09-22
DOI:
EISSN:
2666-1667
Pmid:
37897733


Language:
English
Keywords:
Pubs id:
1556013
Local pid:
pubs:1556013
Deposit date:
2023-11-15

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