Read Merging

Read Merging is a computational procedure in high-throughput sequencing analysis that combines overlapping paired-end reads derived from the same DNA fragment into a single contiguous sequence, thereby improving the accuracy and length of reconstructed 16S ribosomal RNA gene amplicon sequences.

23

Publications

28K

Citations

94

Authors

53

Institutions

Publications per year

2017–2026

11

Variants

Paired-end Read Merging

Authors

94

  1. XK
    Xiuying Kong

    Institute of Crop Sciences, China

    1 publications · 113 citations

    1

    h-index

  2. JD
    Jialei Duan

    The University of Texas Southwestern Medical Center, United States

    1 publications · 113 citations

    1

    h-index

  3. PA
    Piotr A. Mieczkowski

    University of North Carolina at Chapel Hill, United States

    1 publications · 1.1K citations

    1

    h-index

  4. ED
    Erich D. Jarvis

    Howard Hughes Medical Institute, United States

    1 publications · 1.1K citations

    1

    h-index

  5. AL
    Antonio Luna De Haro

    Institut d'Investigació en Ciències de la Salut Germans Trias i Pujol, Spain

    1 publications · 12 citations

    1

    h-index

1–5 of 94

Venues

  1. BMC Bioinformatics

    9 publications · 607 citations

    9

    h-index

  2. Bioinformatics

    4 publications · 20.7K citations

    4

    h-index

  3. Nature Methods

    1 publications · 1.1K citations

    1

    h-index

  4. BMC Research Notes

    1 publications · 2.3K citations

    1

    h-index

  5. Nature Biotechnology

    1 publications · 1.1K citations

    1

    h-index

1–5