Genetic Variant Calling

Genetic Variant Calling is the computational process of identifying differences between an individual grapevine genome and a reference genome, distinguishing itself from general sequence analysis by specifically detecting single nucleotide polymorphisms, insertions, deletions, and structural variants as heritable genetic alterations underlying phenotypic diversity.

80

Publications

7K

Citations

828

Authors

357

Institutions

Publications per year

2017–2026

47

Authors

828

  1. KG
    Kiran Garimella

    Broad Institute, United States

    2 publications · 51 citations

    3

    h-index

  2. EE
    Evan E. Eichler

    University of Washington, United States

    1 publications · 35 citations

    2

    h-index

  3. JD
    Jonathan D. G. Jones

    Sainsbury Laboratory, United Kingdom

    2 publications · 53 citations

    2

    h-index

  4. PK
    Patrik K. E. Magnusson

    Karolinska Institutet, Sweden

    2 publications · 238 citations

    2

    h-index

  5. DC
    Dario Cantù

    University of California, Davis, United States

    1 publications · 18 citations

    2

    h-index

1–5 of 828

Venues

  1. PLoS ONE

    8 publications · 1.1K citations

    8

    h-index

  2. BMC Genomics

    6 publications · 282 citations

    6

    h-index

  3. bioRxiv (Cold Spring Harbor Laboratory)

    Repository · 3 publications · 2.2K citations

    4

    h-index

  4. BMC Bioinformatics

    3 publications · 126 citations

    3

    h-index

  5. Scientific Reports

    3 publications · 87 citations

    3

    h-index

1–5