Duplex Sequencing
Duplex Sequencing is a DNA sequencing method that enhances error detection and correction by independently sequencing both strands of the double helix and requiring consensus between complementary strand reads to validate a variant call.
65
Publications
5K
Citations
433
Authors
159
Institutions
Publications per year
2017–2026
36
Parents
65
Detecting ultralow-frequency mutations by Duplex Sequencing
Scott R. Kennedy, Michael W. Schmitt, Edward Fox et al. · Nature Protocols · 2014 · 539 citations · Full text
Accuracy of Next Generation Sequencing Platforms.
Edward Fox, Kate S. Reid-Bayliss, Mary J. Emond et al. · PubMed · 2014 · 172 citations
Jeffrey D. Krimmel, Michael Schmitt, Maria I. Harrell et al. · Proceedings of the National Academy of Sciences · 2016 · 166 citations · Full text
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433
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8
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159
University of Washington
Seattle, United States
15 h-index
88 publications
13.1K citations

Pennsylvania State University
State College, United States
6 h-index
23 publications
2K citations

University of Washington Medical Center
Seattle, United States
5 h-index
5 publications
428 citations
Harvard University
Cambridge, United States
5 h-index
7 publications
380 citations

Johannes Kepler University of Linz
Linz, Austria
5 h-index
21 publications
609 citations
Blaze Bioscience (United States)
Seattle, United States
4 h-index
13 publications
609 citations
Agricultural Genomics Institute at Shenzhen
Shenzhen, China
4 h-index
6 publications
249 citations
Chinese Academy of Agricultural Sciences
Beijing, China
4 h-index
6 publications
249 citations
1–8 of 159
PNAS · 7 publications · 1.7K citations
7
h-index
5 publications · 303 citations
5
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3 publications · 155 citations
3
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GR · 3 publications · 120 citations
3
h-index
2 publications · 57 citations
2
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