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Minimal methylation classifier (MIMIC): A novel method for derivation and rapid diagnostic detection of disease-associated DNA methylation signatures

Schwalbe, E. C. (author)
Hicks, D. (author)
Rafiee, G. (author)
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Bashton, M. (author)
Gohlke, H. (author)
Enshaei, A. (author)
Potluri, S. (author)
Matthiesen, J. (author)
Mather, M. (author)
Taleongpong, P. (author)
Chaston, R. (author)
Silmon, A. (author)
Curtis, A. (author)
Lindsey, J. C. (author)
Crosier, S. (author)
Smith, A. J. (author)
Goschzik, T. (author)
Doz, F. (author)
Rutkowski, S. (author)
Lannering, Birgitta, 1948 (author)
Gothenburg University,Göteborgs universitet,Institutionen för kliniska vetenskaper, Avdelningen för pediatrik,Institute of Clinical Sciences, Department of Pediatrics
Pietsch, T. (author)
Bailey, S. (author)
Williamson, D. (author)
Clifford, S. C. (author)
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 (creator_code:org_t)
2017-10-18
2017
English.
In: Scientific Reports. - : Springer Science and Business Media LLC. - 2045-2322. ; 7
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Rapid and reliable detection of disease-associated DNA methylation patterns has major potential to advance molecular diagnostics and underpin research investigations. We describe the development and validation of minimal methylation classifier (MIMIC), combining CpG signature design from genome-wide datasets, multiplex-PCR and detection by single-base extension and MALDI-TOF mass spectrometry, in a novel method to assess multi-locus DNA methylation profiles within routine clinically-applicable assays. We illustrate the application of MIMIC to successfully identify the methylation-dependent diagnostic molecular subgroups of medulloblastoma (the most common malignant childhood brain tumour), using scant/low-quality samples remaining from the most recently completed pan-European medulloblastoma clinical trial, refractory to analysis by conventional genome-wide DNA methylation analysis. Using this approach, we identify critical DNA methylation patterns from previously inaccessible cohorts, and reveal novel survival differences between the medulloblastoma disease subgroups with significant potential for clinical exploitation.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)

Keyword

tof mass-spectrometry
medulloblastoma
identification
subgroups
trial
risk
Science & Technology - Other Topics

Publication and Content Type

ref (subject category)
art (subject category)

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