Author

Alexandre Dionne‐Laporte

Montreal Neurological Institute and Hospital

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Genomics· 1

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Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

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Berge Arakel MinassianiD· 1 shared Caroline Meloche· 1 shared Cyrus G. BoelmaniD· 1 shared Dan SpiegelmaniD· 1 shared Danielle Molinari AndradeiD· 1 shared Fadi F. HamdaniD· 1 shared Guillaume BourqueiD· 1 shared Guy Armand RouleauiD· 1 shared

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2018-2018 · peak 1/yr

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Berge Arakel MinassianORCID

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1 paper

Recent·Most cited

GenomicsPLoS GeneticsPeer-reviewedApr 12, 2018

Global characterization of copy number variants in epilepsy patients from whole genome sequencing

Jean Monlong, Simon Girard, Caroline Meloche…·Patrick Cossette

This study uses whole-genome sequencing and a new algorithm to comprehensively characterize copy number variants in epilepsy patients and controls, finding enrichment of rare exonic and non-coding variants.

54 citationstop 3%

humanwhole-genome sequencing

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