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Human copy number variants are enriched in regions of low-mappability
View ORCID ProfileJean Monlong, View ORCID ProfileCaroline Meloche, View ORCID ProfileGuy Rouleau, View ORCID ProfilePatrick Cossette, View ORCID ProfileSimon L. Girard, View ORCID ProfileGuillaume 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
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.
Patrick Cossette
3Centre de Recherche du Centre Hospitalier de l’Université de Montréal, Montreal, H2X 0A9, 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
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Posted December 11, 2015.
Human copy number variants are enriched in regions of low-mappability
Jean Monlong, Caroline Meloche, Guy Rouleau, Patrick Cossette, Simon L. Girard, Guillaume Bourque
bioRxiv 034165; doi: https://doi.org/10.1101/034165
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