Bisulfite Sequencing Analysis

Bisulfite Sequencing Analysis is a genomic analysis method that distinguishes methylated from unmethylated cytosine residues in DNA by leveraging bisulfite conversion, wherein unmethylated cytosines are deaminated to uracil while methylated cytosines remain unchanged, enabling single-nucleotide resolution mapping of DNA methylation patterns across the epigenome.

775

Publications

62.9K

Citations

5.2K

Authors

1.4K

Institutions

Publications per year

2017–2026

239

Authors

5.2K

  1. JW
    Jörn Walter

    Saarland University, Germany

    8 publications · 2.3K citations

    8

    h-index

  2. FL
    Frank Lyko

    German Cancer Research Center, Germany

    8 publications · 1.6K citations

    8

    h-index

  3. RD
    Rajvir Dahiya

    San Francisco VA Medical Center, United States

    8 publications · 797 citations

    8

    h-index

  4. JG
    James G. Herman

    Johns Hopkins University, United States

    7 publications · 543 citations

    7

    h-index

  5. SJ
    Susan J. Clark

    Garvan Institute of Medical Research, Australia

    7 publications · 1K citations

    7

    h-index

1–5 of 5.2K

Venues

  1. PLoS ONE

    42 publications · 2.4K citations

    26

    h-index

  2. PubMed

    Repository · 28 publications · 1.9K citations

    22

    h-index

  3. Nucleic Acids Research

    26 publications · 3K citations

    22

    h-index

  4. Clinical Cancer Research

    18 publications · 1.8K citations

    18

    h-index

  5. Epigenetics

    18 publications · 1.3K citations

    16

    h-index

1–5