Shallow whole-genome sequencing: a useful, easy to apply molecular technique for CNA detection on FFPE tumor tissue—a glioma-driven study.

Detalles Bibliográficos
Publicado en:Virchows Archiv: European Journal of Pathology Vol. 480; no. 3; pp. 677 - 687
Autores principales: Van der Eecken, Kim, Van der Linden, Malaïka, Raman, Lennart, Creytens, David, Dedeurwaerdere, Franceska, De Winne, Koen, Ferdinande, Liesbeth, Lammens, Martin, Menten, Björn, Rottiers, Isabelle, Van Gaever, Bram, Van den Broecke, Caroline, Van de Vijver, Koen, Van Roy, Nadine, Verbeke, Sofie, Van Dorpe, Jo
Formato: Journal Article
Publicado: Springer Nature Mar2022
Acceso en línea:Ver este registro en EBSCOhost
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        atl: Shallow whole-genome sequencing: a useful, easy to apply molecular technique for CNA detection on FFPE tumor tissue—a glioma-driven study.
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          Van der Eecken, Kim
          Van der Linden, Malaïka
          Raman, Lennart
          Creytens, David
          Dedeurwaerdere, Franceska
          De Winne, Koen
          Ferdinande, Liesbeth
          Lammens, Martin
          Menten, Björn
          Rottiers, Isabelle
          Van Gaever, Bram
          Van den Broecke, Caroline
          Van de Vijver, Koen
          Van Roy, Nadine
          Verbeke, Sofie
          Van Dorpe, Jo
        affil: Department of Pathology, Ghent University, Ghent University Hospital, Ghent, Belgium
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      doctype: Journal Article
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