Consensus Sequence Calling

Consensus Sequence Calling is a computational method in genome assembly that determines the most probable nucleotide sequence from aligned reads within an overlap-layout-consensus framework by resolving discrepancies through voting, probabilistic modeling, or error correction.

24

Publications

10.1K

Citations

93

Authors

56

Institutions

Publications per year

2017–2026

9

Authors

93

  1. IS
    Ivan Sović

    Ruđer Bošković Institute, Croatia

    2 publications · 3.5K citations

    2

    h-index

  2. YG
    Yan Gao

    Hubei University of Medicine, China

    2 publications · 67 citations

    2

    h-index

  3. YW
    Yadong Wang

    Harbin Institute of Technology, China

    2 publications · 67 citations

    2

    h-index

  4. WH
    W. H. Day

    Memorial University of Newfoundland, Canada

    2 publications · 32 citations

    2

    h-index

  5. NN
    Niranjan Nagarajan

    Genome Institute of Singapore, Singapore

    2 publications · 3.5K citations

    2

    h-index

1–5 of 93

Venues

  1. bioRxiv (Cold Spring Harbor Laboratory)

    Repository · 4 publications · 147 citations

    4

    h-index

  2. Genome biology

    3 publications · 4.6K citations

    3

    h-index

  3. Bioinformatics

    2 publications · 195 citations

    2

    h-index

  4. Genome Research

    GR · 2 publications · 4.4K citations

    2

    h-index

  5. Nucleic Acids Research

    2 publications · 87 citations

    2

    h-index

1–5