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

Authors

800

  1. WJ
    William J. Greenleaf

    Stanford University, United States

    7 publications · 6.8K citations

    7

    h-index

  2. AK
    Anshul Kundaje

    Stanford University, United States

    4 publications · 3K citations

    4

    h-index

  3. BW
    Beijing Wu

    Stanford University, United States

    3 publications · 6.4K citations

    3

    h-index

  4. NA
    Nicholas A. Sinnott‐Armstrong

    Stanford University, United States

    3 publications · 3K citations

    3

    h-index

  5. SC
    Shengquan Chen

    Tsinghua University, China

    3 publications · 105 citations

    3

    h-index

1–5 of 800

Venues

  1. bioRxiv (Cold Spring Harbor Laboratory)

    Repository · 8 publications · 172 citations

    8

    h-index

  2. Nature Biotechnology

    4 publications · 1.5K citations

    4

    h-index

  3. Nature Methods

    4 publications · 3.2K citations

    4

    h-index

  4. Scientific Reports

    4 publications · 151 citations

    4

    h-index

  5. Arthritis & Rheumatology

    3 publications · 105 citations

    3

    h-index

1–5