Haplotype-Aware Variant Calling is a variant detection methodology that integrates phased haplotype information to improve the accuracy of genetic variant identification by resolving ambiguities arising from sequence homology and structural complexity.
16
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1.4K
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76
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37
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2017–2026
10
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Publications
16
BCFtools/csq: haplotype-aware variant consequences
Petr Danecek, Shane McCarthy · Bioinformatics · 2017 · 504 citations · Full text
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76
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1–5 of 76
Institutions
37
University of New Mexico
Albuquerque, United States
2 h-index
4 publications
94 citations
Wellcome Sanger Institute
Cambridge, United Kingdom
2 h-index
4 publications
1.1K citations
University of California, Santa Cruz
Santa Cruz, United States
2 h-index
13 publications
2.5K citations
Google (United States)
Mountain View, United States
2 h-index
12 publications
2.1K citations
Harvard University
Cambridge, United States
2 h-index
10 publications
1.2K citations
Brigham and Women's Hospital
Boston, United States
2 h-index
5 publications
215 citations
Chan Zuckerberg Initiative (United States)
Redwood City, United States
2 h-index
2 publications
357 citations
University of Oxford
Oxford, United Kingdom
2 h-index
5 publications
270 citations
1–8 of 37
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- bioRxiv (Cold Spring Harbor Laboratory)
Repository · 3 publications · 76 citations
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- Bioinformatics
2 publications · 536 citations
2
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- Nature Biotechnology
2 publications · 287 citations
2
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- Infection Genetics and Evolution
1 publications · 48 citations
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- Forensic Science International Genetics
FSI · 1 publications · 41 citations
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