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Copy number variants calling from WES data through eXome hidden Markov model (XHMM) identifies additional 2.5% pathogenic genomic imbalances smaller than 30 kb undetected by array‐CGH.

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Bibliographic Details
Title:	Copy number variants calling from WES data through eXome hidden Markov model (XHMM) identifies additional 2.5% pathogenic genomic imbalances smaller than 30 kb undetected by array‐CGH.
Authors:	Tisserant, Emilie¹ (AUTHOR), Vitobello, Antonio^1,2 (AUTHOR), Callegarin, Davide² (AUTHOR), Verdez, Simon² (AUTHOR), Bruel, Ange‐line¹ (AUTHOR), Aho Glele, Ludwig Serge³ (AUTHOR), Sorlin, Arthur^1,2 (AUTHOR), Viora‐Dupont, Eleonore² (AUTHOR), Konyukh, Marina² (AUTHOR), Marle, Nathalie² (AUTHOR), Nambot, Sophie^1,3 (AUTHOR), Moutton, Sébastien^1,2,4 (AUTHOR), Racine, Caroline^1,2,5 (AUTHOR), Garde, Aurore^1,2 (AUTHOR), Delanne, Julian^1,5 (AUTHOR), Tran‐Mau‐Them, Frédéric¹ (AUTHOR), Philippe, Christophe^1,2 (AUTHOR), Kuentz, Paul¹ (AUTHOR), Poulleau, Marlène² (AUTHOR), Payet, Muriel² (AUTHOR)
Source:	Annals of Human Genetics. Jul2022, Vol. 86 Issue 4, p171-180. 10p.
Database:	Academic Search Ultimate
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Description
ISSN:	00034800
DOI:	10.1111/ahg.12459