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Human copy number variants are enriched in regions of low-mappability
View ORCID ProfileJean Monlong, Patrick Cossette, Caroline Meloche, View ORCID ProfileGuy Rouleau, View ORCID ProfileSimon L. Girard, Guillaume Bourque
doi: https://doi.org/10.1101/034165
Jean Monlong
1Department of Human Genetics, McGill University, Montréal, H3A 1B1, Canada
2McGill University and Génome Québec Innovation Center, Montréal, H3A 1A4, Canada
Patrick Cossette
3Centre de Recherche du Centre Hospitalier de l’Université de Montréal, Montreal, H2X 0A9, Québec, Canada.
Caroline Meloche
3Centre de Recherche du Centre Hospitalier de l’Université de Montréal, Montreal, H2X 0A9, Québec, Canada.
Guy Rouleau
4Montreal Neurological Institute, McGill University, Montréal, H3A 2B4, Québec, Canada.
Simon L. Girard
1Department of Human Genetics, McGill University, Montréal, H3A 1B1, Canada
5Département des sciences fondamentales, Université du Québec à Chicoutimi, Chicoutimi, G7H 2B1, Canada
Guillaume Bourque
1Department of Human Genetics, McGill University, Montréal, H3A 1B1, Canada
2McGill University and Génome Québec Innovation Center, Montréal, H3A 1A4, Canada
Article usage
Posted May 09, 2016.
Human copy number variants are enriched in regions of low-mappability
Jean Monlong, Patrick Cossette, Caroline Meloche, Guy Rouleau, Simon L. Girard, Guillaume Bourque
bioRxiv 034165; doi: https://doi.org/10.1101/034165
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