Paired-End Sequencing is a high-throughput DNA sequencing strategy in which both ends of a DNA fragment are sequenced to generate two complementary reads separated by a known distance, enabling improved sequence assembly and structural variant detection.
983
Publications
269.5K
Citations
6.7K
Authors
1.7K
Institutions
Publications per year
2017–2026
365
Variants
Paired-end Read Sequencing
Publications
983
Trimmomatic: a flexible trimmer for Illumina sequence data
Anthony Bolger, Marc Lohse, Björn Usadel · Bioinformatics · 2014 · 69.7K citations · Full text
Aligning sequence reads, clone sequences and assembly con*gs with BWA-MEM
Heng Li · arXiv (Cornell University) · 2014 · 5.8K citations · Full text
1–5 of 983
Authors
6.7K
- YR
9
h-index
- İB
9
h-index
- SJSteven J.M. Jones
Canada's Michael Smith Genome Sciences Centre, Canada
8 publications · 5.6K citations
8
h-index
- WS
8
h-index
- JW
8
h-index
1–5 of 6.7K
Institutions
1.7K
Howard Hughes Medical Institute
Chevy Chase, United States
25 h-index
54 publications
11.5K citations
Chinese Academy of Sciences
Beijing, China
21 h-index
140 publications
7.1K citations
Chinese Academy of Agricultural Sciences
Beijing, China
21 h-index
145 publications
46K citations
Stanford University
Stanford, United States
20 h-index
113 publications
15.4K citations
Centre National de la Recherche Scientifique
Paris, France
19 h-index
67 publications
9K citations
Cornell University
Ithaca, United States
17 h-index
63 publications
11.4K citations
BGI Group (China)
Shenzhen, China
16 h-index
135 publications
86.4K citations
Inserm
Paris, France
16 h-index
104 publications
9.7K citations
1–8 of 1.7K
Venues
- PLoS ONE
143 publications · 11.5K citations
54
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- Bioinformatics
82 publications · 130.9K citations
53
h-index
- BMC Genomics
78 publications · 5.6K citations
40
h-index
- BMC Bioinformatics
50 publications · 30.9K citations
30
h-index
- Genome Research
GR · 24 publications · 11.8K citations
23
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