Structural Variation Handling
Structural Variation Handling is a computational method in reference-guided assembly that identifies, characterizes, and incorporates large-scale genomic alterations—such as insertions, deletions, inversions, and translocations—distinguishing itself from standard alignment procedures by explicitly resolving disparities between sequencing reads and the reference genome arising from structural differences.
12
Publications
981
Citations
68
Authors
30
Institutions
Publications per year
2017–2026
6
Parents
12
Efficient assembly of nanopore reads via highly accurate and intact error correction
Ying Chen, Fan Nie, Yingfeng Zheng et al. · Nature Communications · 2021 · 464 citations · Full text
A graph-based approach to diploid genome assembly
Shilpa Garg, Mikko Rautiainen, Adam M. Novak et al. · Bioinformatics · 2018 · 80 citations · Full text
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30

Wellcome Sanger Institute
Cambridge, United Kingdom
2 h-index
4 publications
230 citations
Hainan University
Haikou, China
1 h-index
1 publications
464 citations

Ghent University
Ghent, Belgium
1 h-index
9 publications
558 citations

Siriraj Hospital
Bangkok, Thailand
1 h-index
1 publications
27 citations

Universidad de Murcia
Murcia, Spain
1 h-index
3 publications
51 citations

University of Helsinki
Helsinki, Finland
1 h-index
3 publications
285 citations
Oxford Nanopore Technologies (United Kingdom)
Oxford, United Kingdom
1 h-index
1 publications
464 citations
National Center for Genetic Engineering and Biotechnology
Pathum Thani, Thailand
1 h-index
7 publications
189 citations
1–8 of 30
2 publications · 41 citations
2
h-index
1 publications · 88 citations
1
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Book series · 1 publications · 35 citations
1
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TKDE · 1 publications · 17 citations
1
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1 publications · 80 citations
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