Translocation Detection

Translocation Detection is a computational method in structural variant analysis that identifies chromosomal rearrangements involving the exchange of genetic material between non-homologous chromosomes, distinguishing it from other variant detection approaches by its specific focus on inter-chromosomal breakpoints.

131

Publications

6.1K

Citations

768

Authors

285

Institutions

Publications per year

2017–2026

18

Authors

768

  1. SM
    S. Munné

    Reprogenetics, United States

    4 publications · 176 citations

    4

    h-index

  2. FS
    Frank Speleman

    Ghent University Hospital, Belgium

    4 publications · 94 citations

    4

    h-index

  3. JH
    Jochen Harbott

    Justus-Liebig-Universität Gießen, Germany

    3 publications · 54 citations

    3

    h-index

  4. MP
    M. Poggensee

    Lawrence Livermore National Laboratory, United States

    3 publications · 567 citations

    3

    h-index

  5. YL
    Yi‐Tao Long

    East China University of Science and Technology, China

    3 publications · 128 citations

    3

    h-index

1–5 of 768

Venues

  1. PubMed

    Repository · 17 publications · 740 citations

    14

    h-index

  2. Genes Chromosomes and Cancer

    7 publications · 353 citations

    7

    h-index

  3. Human Genetics

    7 publications · 330 citations

    7

    h-index

  4. Blood

    6 publications · 284 citations

    6

    h-index

  5. British Journal of Haematology

    BJH · 4 publications · 81 citations

    4

    h-index

1–5