Chromatin Accessibility Sequencing
Chromatin Accessibility Sequencing is a genomic profiling technique that identifies regions of open chromatin by selectively sequencing DNA segments accessible to regulatory proteins, thereby enabling the inference of gene regulatory elements and transcriptional activity.
81
Publications
13.3K
Citations
800
Authors
275
Institutions
Publications per year
2017–2026
74
Parents
81
A Single-Cell Atlas of In Vivo Mammalian Chromatin Accessibility
Darren A. Cusanovich, Andrew J. Hill, Delasa Aghamirzaie et al. · Cell · 2018 · 889 citations · Full text
Microanatomy of the Human Atherosclerotic Plaque by Single-Cell Transcriptomics
Marie A.C. Depuydt, Koen H.M. Prange, Lotte Slenders et al. · Circulation Research · 2020 · 581 citations · Full text
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Stanford University
Stanford, United States
11 h-index
85 publications
79K citations
Chan Zuckerberg Initiative (United States)
Redwood City, United States
5 h-index
5 publications
3.1K citations
University of Chinese Academy of Sciences
Beijing, China
4 h-index
18 publications
436 citations
University of Washington
Seattle, United States
4 h-index
31 publications
14.5K citations

Howard Hughes Medical Institute
Chevy Chase, United States
4 h-index
5 publications
8.8K citations

Chinese Academy of Sciences
Beijing, China
3 h-index
13 publications
498 citations
University of California San Diego
San Diego, United States
3 h-index
5 publications
3.3K citations
Stanford Medicine
Stanford, United States
3 h-index
3 publications
339 citations
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Repository · 8 publications · 172 citations
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4 publications · 1.5K citations
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4 publications · 3.2K citations
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4 publications · 151 citations
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3 publications · 105 citations
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