Read Pairing

Read Pairing is a computational method in read mapping that distinguishes itself by identifying and aligning two complementary DNA sequence reads originating from opposite ends of the same genomic fragment to their respective locations in a reference genome.

13

Publications

6.1K

Citations

68

Authors

38

Institutions

Publications per year

2017–2026

7

Variants

Paired-end Mapping

Authors

68

  1. JS
    Jan Schröder

    The University of Melbourne, Australia

    2 publications · 511 citations

    2

    h-index

  2. HD
    Hongdo Do

    The University of Melbourne, Australia

    2 publications · 511 citations

    2

    h-index

  3. AD
    Alexander Dobrovic

    The University of Melbourne, Australia

    2 publications · 511 citations

    2

    h-index

  4. TP
    Terence P. Speed

    Walter and Eliza Hall Institute of Medical Research, Australia

    2 publications · 511 citations

    2

    h-index

  5. DC
    Daniel Cameron

    Walter and Eliza Hall Institute of Medical Research, Australia

    2 publications · 511 citations

    2

    h-index

1–5 of 68

Venues

  1. Bioinformatics

    7 publications · 5.3K citations

    7

    h-index

  2. bioRxiv (Cold Spring Harbor Laboratory)

    Repository · 2 publications · 59 citations

    2

    h-index

  3. Genome Research

    GR · 1 publications · 462 citations

    1

    h-index

  4. Current Protocols in Bioinformatics

    1 publications · 193 citations

    1

    h-index

  5. BMC Bioinformatics

    1 publications · 14 citations

    1

    h-index

1–5