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Author Details
Full Name
John W Belmont
Affiliation
Illumina Inc.
ORCID
Career Start Year
2007
Papers
3
H Index
3
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
30293986
Copy-number variants in clinical genome sequencing: deployment and interpretation for rare and undiagnosed disease.
Genet Med
2019
17943122
A second generation human haplotype map of over 3.1 million SNPs.
Nature
2007
17943131
Genome-wide detection and characterization of positive selection in human populations.
Nature
2007
1 - 3 of 3
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McGill University
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William Harvey Research Institute, Queen Mary University of London
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