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Method: DNA copy number analysis of fresh and formalin-fixed specimens by shallow whole-genome sequencing with identification and exclusion of problematic regions in the genome assembly

Ilari Scheinin,
Daoud Sie,
Henrik Bengtsson,
Mark A van de Wiel,
Adam B Olshen,
Hinke F van Thuijl,
Hendrik F van Essen,
Paul P Eijk,
Francois Rustenburg,
Gerrit A Meijer,
Jaap C Reijneveld,
Pieter Wesseling,
Daniel Pinkel,
Donna G Albertson,
and Bauke Ylstra

Genome Res. September 18, 2014 gr.175141.114; Published in Advance September 18, 2014, doi:10.1101/gr.175141.114

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