Multi Sample Variant Calling is a variant calling method that simultaneously analyzes genomic data from multiple individuals to jointly infer genetic variants, leveraging shared information across samples to improve accuracy and consistency compared to single-sample approaches.
36
Publications
4.4K
Citations
311
Authors
118
Institutions
Publications per year
2017–2026
14
Parents
Publications
36
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
Variant Callers for Next-Generation Sequencing Data: A Comparison Study
Xiangtao Liu, Shizhong Han, Zuoheng Wang et al. · PLoS ONE · 2013 · 178 citations · Full text
1–5 of 36
Authors
311
- MC
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- KN
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- US
2
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- SF
2
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- AR
2
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1–5 of 311
Institutions
118
Harvard University
Cambridge, United States
6 h-index
10 publications
1.2K citations
Massachusetts General Hospital
Boston, United States
4 h-index
17 publications
14.4K citations
University of Washington
Seattle, United States
4 h-index
8 publications
912 citations
University of Oxford
Oxford, United Kingdom
3 h-index
6 publications
358 citations
Illumina (United States)
San Diego, United States
3 h-index
21 publications
1.9K citations
Broad Institute
Cambridge, United States
3 h-index
25 publications
43.9K citations
Center for Human Genetics
Bar Harbor, United States
2 h-index
2 publications
251 citations
Centre for Human Genetics
Oxford, United Kingdom
2 h-index
4 publications
282 citations
1–8 of 118
Venues
- Bioinformatics
5 publications · 287 citations
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- BMC Bioinformatics
5 publications · 202 citations
5
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- PLoS ONE
5 publications · 541 citations
5
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- bioRxiv (Cold Spring Harbor Laboratory)
Repository · 4 publications · 2.4K citations
4
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- BMC Genomics
3 publications · 270 citations
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