Somatic Variant Calling

Somatic Variant Calling is a computational method in variant calling that identifies acquired genetic mutations present in tumor cells but absent in the germline genome of the same individual, distinguishing it from germline variant detection by focusing on somatic alterations associated with cancer development.

108

Publications

16.1K

Citations

966

Authors

304

Institutions

Publications per year

2017–2026

77

Authors

966

  1. CT
    Christopher T. Saunders

    Illumina (United States), United States

    4 publications · 6K citations

    4

    h-index

  2. GL
    Gerton Lunter

    University of Oxford, United Kingdom

    3 publications · 155 citations

    3

    h-index

  3. MM
    Marghoob Mohiyuddin

    Stanford University, United States

    3 publications · 331 citations

    3

    h-index

  4. OL
    Obi L. Griffith

    Washington University in St. Louis, United States

    3 publications · 222 citations

    3

    h-index

  5. MK
    Morten Källberg

    Illumina (United Kingdom), United Kingdom

    3 publications · 4.3K citations

    3

    h-index

1–5 of 966

Venues

  1. Bioinformatics

    10 publications · 5.2K citations

    10

    h-index

  2. bioRxiv (Cold Spring Harbor Laboratory)

    Repository · 13 publications · 1.1K citations

    10

    h-index

  3. Genome biology

    7 publications · 519 citations

    7

    h-index

  4. BMC Bioinformatics

    6 publications · 164 citations

    6

    h-index

  5. PLoS ONE

    5 publications · 390 citations

    5

    h-index

1–5