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@ARTICLE{Ryzhova:178293,
      author       = {M. V. Ryzhova and E. N. Telysheva and E. G. Shaikhaev and
                      D. V. Starovoitov and A. O. Kotelnikova and S. A. Galstyan
                      and K. Okonechnikov$^*$},
      title        = {{S}ovremennye diagnosticheskie vozmozhnosti molekulyarnogo
                      issledovaniya opukholei mozga v {T}sentre neirokhirurgii im.
                      akad. {N}.{N}. {B}urdenko.},
      journal      = {Zurnal voprosy nejrochirurgii imeni N.N. Burdenko},
      volume       = {85},
      number       = {6},
      issn         = {0042-8817},
      address      = {Moskva},
      publisher    = {Nakl. Medicina},
      reportid     = {DKFZ-2021-03240},
      pages        = {98},
      year         = {2021},
      note         = {#LA:B062#},
      abstract     = {DnA methylation has recently been accepted as the most
                      reliable and effective method of diagnosing central nervous
                      system (CNS) tumors. Healthy organs and tumors of different
                      localizations have their own unique methylation structure.
                      Determination of total tumor DNA methylome is the detection
                      of all methylated nucleotides in a tumor. The 'gold
                      standard' for analyzing the methylation state of individual
                      cytosines is bisulfite conversion, in which unmethylated
                      cytosines are converted to uracils and read as thymines,
                      while methylated cytosines are protected from conversion.},
      keywords     = {Brain Neoplasms: genetics / DNA: metabolism / DNA
                      Methylation / Humans / DNA methylation (Other) / EPIC array
                      (Other) / Illumina Infinium HumanMethylation850 BeadChip
                      (Other) / DNA (NLM Chemicals)},
      cin          = {B062},
      ddc          = {610},
      cid          = {I:(DE-He78)B062-20160331},
      pnm          = {312 - Funktionelle und strukturelle Genomforschung
                      (POF4-312)},
      pid          = {G:(DE-HGF)POF4-312},
      typ          = {PUB:(DE-HGF)16},
      pubmed       = {pmid:34951766},
      doi          = {10.17116/neiro20218506198},
      url          = {https://inrepo02.dkfz.de/record/178293},
}