Population Variant Calling
Population Variant Calling is a computational genomics method that identifies genetic variants across multiple individuals simultaneously by leveraging shared patterns of variation within a population to improve accuracy and resolve rare alleles.
47
Publications
6.8K
Citations
1.4K
Authors
160
Institutions
Publications per year
2017–2026
17
Parents
47
Detection of large-scale variation in the human genome
A. John Iafrate, Lars Feuk, Miguel N. Rivera et al. · Nature Genetics · 2004 · 2.9K citations
PopGene32, Microsoft windows-based freeware for population genetic analysis. Version 1.32
Detection of mosaic and population-level structural variants with Sniffles2
Moritz Smolka, Luis F. Paulin, Christopher M. Grochowski et al. · Nature Biotechnology · 2024 · 439 citations · Full text
Comprehensive variation discovery in single human genomes
Neil Weisenfeld, Shuangye Yin, Ted Sharpe et al. · Nature Genetics · 2014 · 247 citations · Full text
Best Practices and Joint Calling of the HumanExome BeadChip: The CHARGE Consortium
Megan L. Grove, Bing Yu, Barbara Cochran et al. · PLoS ONE · 2013 · 238 citations · Full text
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160
Harvard University
Cambridge, United States
8 h-index
51 publications
16.3K citations

Broad Institute
Cambridge, United States
6 h-index
70 publications
8.7K citations

Johns Hopkins University
Baltimore, United States
4 h-index
9 publications
1.2K citations
Baylor College of Medicine
Houston, United States
4 h-index
22 publications
4.7K citations
Massachusetts General Hospital
Boston, United States
4 h-index
16 publications
4.4K citations

Rice University
Houston, United States
3 h-index
3 publications
563 citations
Scripps Research Institute
San Diego, United States
3 h-index
11 publications
977 citations

Washington University in St. Louis
St Louis, United States
2 h-index
11 publications
508 citations
1–8 of 160
5 publications · 122 citations
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5 publications · 423 citations
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3 publications · 235 citations
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3 publications · 77 citations
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2 publications · 60 citations
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