Concepedia

Paired-end Mapping

Paired-End Mapping is a genomic analysis method that belongs to the class of structural variation detection techniques, differing from other methods by leveraging the aligned distance and orientation of paired sequencing reads to identify structural variants such as deletions, insertions, inversions, and translocations.

43

Publications

5.5K

Citations

251

Authors

124

Institutions

Publications per year

2017–2026

9

Parents

Publications

43

Paired-End Mapping Reveals Extensive Structural Variation in the Human Genome

Jan O. Korbel, Alexander E. Urban, Jason P. Affourtit et al. · Science · 2007 · 1.2K citations · Full text

, , +17

Sensitive and accurate detection of copy number variants using read depth of coverage

Seungtai Yoon, Zhenyu Xuan, Vladimir Makarov et al. · Genome Research · 2009 · 655 citations · Full text

, , +17

AdapterRemoval: easy cleaning of next-generation sequencing reads

Stinus Lindgreen · BMC Research Notes · 2012 · 651 citations · Full text

, , +15

Genome-wide mapping and assembly of structural variant breakpoints in the mouse genome

Aaron R. Quinlan, Royden A. Clark, Svetlana Sokolova et al. · Genome Research · 2010 · 300 citations · Full text

, , +16

FusionMap: detecting fusion genes from next-generation sequencing data at base-pair resolution

Huanying Ge, Kejun Liu, Todd Juan et al. · Bioinformatics · 2011 · 287 citations

, , +17

1–5 of 43

Authors

251

  1. MB
    Michael Brudno

    University of Toronto, Canada

    3 publications · 343 citations

    3

    h-index

  2. ME
    Matthew E. Hurles

    Wellcome Sanger Institute, United Kingdom

    2 publications · 1.5K citations

    2

    h-index

  3. JO
    Jan O. Korbel

    European Molecular Biology Laboratory, Germany

    2 publications · 1.5K citations

    2

    h-index

  4. NC
    Nicholas Carriero

    Yale University, United States

    2 publications · 1.5K citations

    2

    h-index

  5. MG
    Mark Gerstein

    Yale University, United States

    2 publications · 1.5K citations

    2

    h-index

1–5 of 251

Institutions

124

  1. University of Toronto

    Toronto, Canada

    3 h-index

    3 publications

    343 citations

  2. Yale University

    New Haven, United States

    2 h-index

    2 publications

    1.5K citations

  3. European Molecular Biology Laboratory

    Heidelberg, Germany

    2 h-index

    2 publications

    1.5K citations

  4. Cold Spring Harbor Laboratory

    Cold Spring Harbor, United States

    2 h-index

    2 publications

    727 citations

  5. Wellcome Sanger Institute

    Cambridge, United Kingdom

    2 h-index

    2 publications

    354 citations

  6. Max Planck Institute for Molecular Genetics

    Berlin, Germany

    2 h-index

    2 publications

    327 citations

  7. RIKEN Center for Integrative Medical Sciences

    Yokohama, Japan

    2 h-index

    2 publications

    313 citations

  8. Centre for Human Genetics

    Oxford, United Kingdom

    2 h-index

    2 publications

    162 citations

1–8 of 124

Venues

  1. Bioinformatics

    7 publications · 648 citations

    7

    h-index

  2. BMC Genomics

    5 publications · 135 citations

    5

    h-index

  3. Genome Research

    GR · 4 publications · 1.2K citations

    4

    h-index

  4. Science

    2 publications · 1.4K citations

    2

    h-index

  5. Genome biology

    2 publications · 328 citations

    2

    h-index

1–5