Long-read Sequencing

Long-Read Sequencing is a genomic sequencing technology that belongs to the class of DNA sequencing methods and is distinguished by its ability to generate continuous reads spanning thousands to hundreds of thousands of base pairs, enabling the resolution of complex genomic regions such as repetitive sequences, structural variants, and haplotype phasing with greater accuracy than short-read approaches.

1.4K

Publications

118.4K

Citations

11K

Authors

2.5K

Institutions

Publications per year

2017–2026

1.3K

Authors

11K

  1. EE
    Evan E. Eichler

    University of Washington, United States

    37 publications · 9.1K citations

    27

    h-index

  2. AM
    Adam M. Phillippy

    National Human Genome Research Institute, United States

    29 publications · 7.1K citations

    23

    h-index

  3. SK
    Sergey Koren

    National Human Genome Research Institute, United States

    28 publications · 6.8K citations

    22

    h-index

  4. FJ
    Fritz J. Sedlazeck

    Baylor College of Medicine, United States

    22 publications · 2.6K citations

    20

    h-index

  5. MC
    Michael C. Schatz

    Johns Hopkins University, United States

    20 publications · 2.2K citations

    19

    h-index

1–5 of 11K

Venues

  1. Nature Communications

    62 publications · 6.8K citations

    42

    h-index

  2. bioRxiv (Cold Spring Harbor Laboratory)

    Repository · 139 publications · 5.2K citations

    36

    h-index

  3. Bioinformatics

    43 publications · 8.8K citations

    31

    h-index

  4. BMC Genomics

    65 publications · 2.8K citations

    31

    h-index

  5. Genome biology

    40 publications · 6.1K citations

    30

    h-index

1–5