Single-cell Long-read Sequencing

Single-Cell Long-Read Sequencing is a genomic methodology that enables the comprehensive analysis of full-length nucleic acid molecules at the resolution of individual cells, thereby preserving haplotype information and enabling precise characterization of transcript isoforms, structural variants, and epigenetic modifications within heterogeneous cell populations.

39

Publications

2.9K

Citations

437

Authors

149

Institutions

Publications per year

2017–2026

36

Authors

437

  1. AJ
    Anoushka Joglekar

    Cornell University, United States

    4 publications · 382 citations

    4

    h-index

  2. HT
    Hagen Tilgner

    Cornell University, United States

    4 publications · 382 citations

    4

    h-index

  3. QG
    Quentin Gouil

    The University of Melbourne, Australia

    3 publications · 349 citations

    3

    h-index

  4. ME
    M. Elizabeth Ross

    Cornell University, United States

    3 publications · 354 citations

    3

    h-index

  5. FR
    Fairlie Reese

    University of California, Irvine, United States

    3 publications · 796 citations

    3

    h-index

1–5 of 437

Venues

  1. Nature Communications

    6 publications · 510 citations

    6

    h-index

  2. bioRxiv (Cold Spring Harbor Laboratory)

    Repository · 5 publications · 112 citations

    5

    h-index

  3. Genome biology

    3 publications · 468 citations

    3

    h-index

  4. Science

    2 publications · 109 citations

    2

    h-index

  5. Bioinformatics

    2 publications · 59 citations

    2

    h-index

1–5