Consensus Sequence Calling
Consensus Sequence Calling is a computational method in genome assembly that determines the most probable nucleotide sequence from aligned reads within an overlap-layout-consensus framework by resolving discrepancies through voting, probabilistic modeling, or error correction.
24
Publications
10.1K
Citations
93
Authors
56
Institutions
Publications per year
2017–2026
9
24
Fast and accurate de novo genome assembly from long uncorrected reads
Robert Vaser, Ivan Sović, Niranjan Nagarajan et al. · Genome Research · 2017 · 3.4K citations · Full text
Accuracy and quality of massively parallel DNA pyrosequencing
Susan M. Huse, Julie A. Huber, Hilary G. Morrison et al. · Genome biology · 2007 · 1.3K citations · Full text
Life Sciences, Biology, Microbiology +17
SNP detection for massively parallel whole-genome resequencing
Ruiqiang Li, Yingrui Li, Xiaodong Fang et al. · Genome Research · 2009 · 957 citations · Full text
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56

University of Louisville
Louisville, United States
2 h-index
2 publications
32 citations

University of Zagreb
Zagreb, Croatia
2 h-index
4 publications
7K citations
Bioinformatics Institute
Singapore, Singapore
2 h-index
2 publications
3.5K citations
Genome Institute of Singapore
Singapore, Singapore
2 h-index
2 publications
3.5K citations
University of California, Berkeley
Berkeley, United States
2 h-index
3 publications
149 citations

Harbin Institute of Technology
Harbin, China
2 h-index
10 publications
335 citations
Memorial University of Newfoundland
St. John's, Canada
2 h-index
2 publications
32 citations
London School of Hygiene & Tropical Medicine
London, United Kingdom
2 h-index
2 publications
3.4K citations
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Repository · 4 publications · 147 citations
4
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3 publications · 4.6K citations
3
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2 publications · 195 citations
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GR · 2 publications · 4.4K citations
2
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2 publications · 87 citations
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