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Methylation microarray-based detection of clinical copy-number aberrations in CLL benchmarked to standard FISH analysis.
Hussmann, Dianna; Starnawska, Anna; Kristensen, Louise; Daugaard, Iben; Cédile, Oriane; Nguyen, Vivi Quoc; Kjeldsen, Tina E; Hansen, Christine Søholm; Bybjerg-Grauholm, Jonas; Kristensen, Thomas; Larsen, Thomas Stauffer; Møller, Michael Boe; Nyvold, Charlotte Guldborg; Hansen, Lise Lotte; Wojdacz, Tomasz K.
Afiliación
  • Hussmann D; Department of Biomedicine, Aarhus University, Aarhus, Denmark.
  • Starnawska A; Department of Biomedicine, Aarhus University, Aarhus, Denmark; The Lundbeck Foundation Initiative for Integrative Psychiatric Research, iPSYCH, Denmark; Center for Integrative Sequencing, iSEQ, Aarhus University, Aarhus, Denmark; Centre for Genomics and Personalized Medicine, CGPM, Aarhus University
  • Kristensen L; Department of Pathology, Odense University Hospital, Odense, Denmark.
  • Daugaard I; Department of Biomedicine, Aarhus University, Aarhus, Denmark; Department of Pathology, Aarhus University Hospital, Aarhus, Denmark.
  • Cédile O; Haematology-Pathology Research Laboratory, Research Unit for Haematology and Research Unit for Pathology, University of Southern Denmark and Odense University Hospital, Odense, Denmark.
  • Nguyen VQ; Department of Pathology, Odense University Hospital, Odense, Denmark.
  • Kjeldsen TE; Department of Biomedicine, Aarhus University, Aarhus, Denmark.
  • Hansen CS; The Lundbeck Foundation Initiative for Integrative Psychiatric Research, iPSYCH, Denmark; Department for Congenital Disorders, Statens Serum Institut, Copenhagen, Denmark; Department of Psychiatry, Mount Sinai, New York, NY, USA.
  • Bybjerg-Grauholm J; The Lundbeck Foundation Initiative for Integrative Psychiatric Research, iPSYCH, Denmark; Department for Congenital Disorders, Statens Serum Institut, Copenhagen, Denmark.
  • Kristensen T; Department of Pathology, Odense University Hospital, Odense, Denmark; Department of Clinical Development, Odense University Hospital, Odense, Denmark.
  • Larsen TS; Department of Haematology, Odense University Hospital, Odense, Denmark.
  • Møller MB; Department of Pathology, Odense University Hospital, Odense, Denmark; Haematology-Pathology Research Laboratory, Research Unit for Haematology and Research Unit for Pathology, University of Southern Denmark and Odense University Hospital, Odense, Denmark.
  • Nyvold CG; Haematology-Pathology Research Laboratory, Research Unit for Haematology and Research Unit for Pathology, University of Southern Denmark and Odense University Hospital, Odense, Denmark.
  • Hansen LL; Department of Biomedicine, Aarhus University, Aarhus, Denmark.
  • Wojdacz TK; Department of Biomedicine, Aarhus University, Aarhus, Denmark; Aarhus Institute of Advanced Studies, Aarhus University, Aarhus, Denmark; Independent Clinical Epigenetics Laboratory, Pomeranian Medical University, Szczecin, Poland. Electronic address: Tomasz.wojdacz@pum.edu.pl.
Genomics ; 114(6): 110510, 2022 11.
Article en En | MEDLINE | ID: mdl-36272495
Copy-number aberrations (CNAs) are assessed using FISH analysis in diagnostics of chronic lymphocytic leukemia (CLL), but CNAs can also be extrapolated from Illumina BeadChips developed for genome-wide methylation microarray screening. Increasing numbers of microarray data-sets are available from diagnostic samples, making it useful to assess the potential in CNA diagnostics. We benchmarked the limitations of CNA testing from two Illumina BeadChips (EPIC and 450k) and using two common packages for analysis (conumee and ChAMP) to FISH-based assessment of 11q, 13q, and 17p deletions in 202 CLL samples. Overall, the two packages predicted CNAs with similar accuracy regardless of the microarray type, but lower than FISH-based assessment. We showed that the bioinformatics analysis needs to be adjusted to the specific CNA, as no general settings were identified. Altogether, we were able to predict CNAs using methylation microarray data, however, with limited accuracy, making FISH-based assessment of deletions the superior diagnostic choice.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Leucemia Linfocítica Crónica de Células B Tipo de estudio: Diagnostic_studies Límite: Humans Idioma: En Revista: Genomics Asunto de la revista: GENETICA Año: 2022 Tipo del documento: Article País de afiliación: Dinamarca Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Leucemia Linfocítica Crónica de Células B Tipo de estudio: Diagnostic_studies Límite: Humans Idioma: En Revista: Genomics Asunto de la revista: GENETICA Año: 2022 Tipo del documento: Article País de afiliación: Dinamarca Pais de publicación: Estados Unidos