Genetic Variant Calling
Genetic Variant Calling is the computational process of identifying differences between an individual grapevine genome and a reference genome, distinguishing itself from general sequence analysis by specifically detecting single nucleotide polymorphisms, insertions, deletions, and structural variants as heritable genetic alterations underlying phenotypic diversity.
80
Publications
7K
Citations
828
Authors
357
Institutions
Publications per year
2017–2026
47
Parents
80
Unified representation of genetic variants
Adrian Tan, Gonçalo R. Abecasis, Hyun Min Kang · Bioinformatics · 2015 · 470 citations · Full text
Clinical Interpretation and Implications of Whole-Genome Sequencing
Frederick E. Dewey, Megan E. Grove, Cuiping Pan et al. · JAMA · 2014 · 459 citations · Full text
The Draft Genome Sequence of European Pear (Pyrus communis L. ‘Bartlett’)
David Chagné, Ross Crowhurst, Massimo Pindo et al. · PLoS ONE · 2014 · 333 citations · Full text
1–5 of 80
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357

Centre for Human Genetics
Oxford, United Kingdom
5 h-index
10 publications
205 citations
University of Oxford
Oxford, United Kingdom
5 h-index
15 publications
309 citations

Broad Institute
Cambridge, United States
5 h-index
32 publications
43K citations
University of California, Davis
Davis, United States
4 h-index
14 publications
554 citations
University of Washington
Seattle, United States
4 h-index
14 publications
1.3K citations
Heinrich Heine University Düsseldorf
Düsseldorf, Germany
3 h-index
5 publications
137 citations
United States Department of Agriculture
Washington, United States
3 h-index
9 publications
1.1K citations

University of Minnesota
Minneapolis, United States
3 h-index
5 publications
200 citations
1–8 of 357
8 publications · 1.1K citations
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6 publications · 282 citations
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Repository · 3 publications · 2.2K citations
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3 publications · 126 citations
3
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3 publications · 87 citations
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