Read Bridging
Read Bridging is a computational strategy in genome finishing that belongs to the class of sequence assembly refinement methods, distinguished by its use of overlapping or paired-end reads to span gaps between contiguous sequences and resolve repetitive or ambiguous regions.
4
Publications
501
Citations
22
Authors
9
Institutions
Publications per year
2017–2026
2
Parents
4
ARCS: scaffolding genome drafts with linked reads
Sarah Yeo, Lauren Coombe, René L. Warren et al. · Bioinformatics · 2017 · 234 citations · Full text
COPE: an accurate <i>k</i>-mer-based pair-end reads connection tool to facilitate genome assembly
Binghang Liu, Jianying Yuan, Siu‐Ming Yiu et al. · Bioinformatics · 2012 · 146 citations · Full text
DENTIST—using long reads for closing assembly gaps at high accuracy
Arne Ludwig, Martin Pippel, Michael Hiller · GigaScience · 2022 · 29 citations · Full text
1–4 of 4
22
1
h-index
1
h-index
1
h-index
1
h-index
1
h-index
1–5 of 22
9

Senckenberg Research Institute and Natural History Museum Frankfurt/M
Frankfurt am Main, Germany
1 h-index
1 publications
29 citations
Goethe University Frankfurt
Frankfurt am Main, Germany
1 h-index
1 publications
29 citations
LOEWE Centre for Translational Biodiversity Genomics
Frankfurt am Main, Germany
1 h-index
1 publications
29 citations

University of Hong Kong
Pok Fu Lam, Hong Kong
1 h-index
11 publications
1.6K citations
Technical University of Munich
Munich, Germany
1 h-index
3 publications
276 citations
Center for Systems Biology Dresden
Dresden, Germany
1 h-index
3 publications
87 citations
Max Planck Institute of Molecular Cell Biology and Genetics
Dresden, Germany
1 h-index
3 publications
87 citations
Chinese University of Hong Kong, Shenzhen
Shenzhen, China
1 h-index
11 publications
1.6K citations
1–8 of 9
2 publications · 380 citations
2
h-index
1 publications · 92 citations
1
h-index
1 publications · 29 citations
1
h-index
1–3