Short-read Sequencing

Short-Read Sequencing is a genome sequencing methodology that generates highly accurate sequence reads of relatively short length, typically ranging from 50 to 300 base pairs, by massively parallel sequencing of fragmented DNA templates to enable high-throughput reconstruction of genomic sequences.

1.1K

Publications

300K

Citations

8.1K

Authors

1.9K

Institutions

Publications per year

2017–2026

795

Authors

8.1K

  1. EE
    Evan E. Eichler

    University of Washington, United States

    22 publications · 4.3K citations

    21

    h-index

  2. FJ
    Fritz J. Sedlazeck

    Baylor College of Medicine, United States

    21 publications · 3.3K citations

    20

    h-index

  3. MC
    Michael C. Schatz

    Johns Hopkins University, United States

    19 publications · 4.6K citations

    19

    h-index

  4. MC
    Mark Chaisson

    University of Southern California, United States

    14 publications · 2.9K citations

    14

    h-index

  5. AM
    Adam M. Phillippy

    National Human Genome Research Institute, United States

    17 publications · 2.1K citations

    14

    h-index

1–5 of 8.1K

Venues

  1. Bioinformatics

    89 publications · 155.6K citations

    50

    h-index

  2. Genome Research

    GR · 49 publications · 14.5K citations

    37

    h-index

  3. Nature Communications

    50 publications · 5.9K citations

    37

    h-index

  4. PLoS ONE

    54 publications · 5.7K citations

    34

    h-index

  5. BMC Genomics

    63 publications · 4.2K citations

    34

    h-index

1–5