Indel Realignment

Indel Realignment is a computational method in the field of genomic variant calling that realigns sequencing reads around insertion and deletion (indel) loci to minimize alignment artifacts and improve the accuracy of variant detection by correcting misalignments caused by indels.

14

Publications

976

Citations

82

Authors

25

Institutions

Publications per year

2017–2026

5

Authors

82

  1. JS
    Joel S. Parker

    University of North Carolina at Chapel Hill, United States

    2 publications · 273 citations

    2

    h-index

  2. CM
    Charles M. Perou

    University of North Carolina at Chapel Hill, United States

    2 publications · 273 citations

    2

    h-index

  3. LE
    Lisle E. Mose

    The University of Texas MD Anderson Cancer Center, United States

    2 publications · 273 citations

    2

    h-index

  4. JL
    Jiankang Li

    BGI Group (China), China

    1 publications · 10 citations

    1

    h-index

  5. JW
    Jian Wu

    Institute of Vegetables and Flowers, China

    1 publications · 124 citations

    1

    h-index

1–5 of 82

Venues

  1. Bioinformatics

    3 publications · 301 citations

    3

    h-index

  2. 1

    h-index

  3. International Journal of Ophthalmology

    IJO · 1 publications · 10 citations

    1

    h-index

  4. BMC Genomics

    1 publications · 34 citations

    1

    h-index

  5. Nature Precedings

    1 publications · 17 citations

    1

    h-index

1–5