Linked-read Haplotype Assembly

Linked-Read Haplotype Assembly is a haplotype-resolved genome assembly method that leverages barcoded short reads from linked-read sequencing technologies to partition and reconstruct haplotype-specific genomic regions by associating reads sharing common molecular barcodes with individual homologous chromosomes.

14

Publications

1.2K

Citations

195

Authors

57

Institutions

Publications per year

2017–2026

13

Authors

195

  1. JI
    Joana I. Meier

    University of Cambridge, United Kingdom

    2 publications · 137 citations

    2

    h-index

  2. RW
    R. W. Davies

    University of Oxford, United Kingdom

    2 publications · 137 citations

    2

    h-index

  3. MK
    Marek Kučka

    Eunice Kennedy Shriver National Institute of Child Health and Human Development, United States

    2 publications · 137 citations

    2

    h-index

  4. PK
    Pui–Yan Kwok

    University of California, San Francisco, United States

    2 publications · 259 citations

    2

    h-index

  5. VB
    Vikas Bansal

    University of California San Diego, United States

    2 publications · 599 citations

    2

    h-index

1–5 of 195

Venues

  1. Proceedings of the National Academy of Sciences

    PNAS · 2 publications · 270 citations

    2

    h-index

  2. Genome Research

    GR · 2 publications · 599 citations

    2

    h-index

  3. Nature Communications

    1 publications · 101 citations

    1

    h-index

  4. BMC Bioinformatics

    1 publications · 17 citations

    1

    h-index

  5. Bioinformatics Advances

    1 publications · 14 citations

    1

    h-index

1–5