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The prognostic significance of single-nucleotide polymorphism array-based whole-genome analysis and uniparental disomy in myelodysplastic syndrome.

Yang OuYan YangHongbin YuXin ZhangMin LiuYu Wu
Published in: International journal of laboratory hematology (2021)
Compared with MC, SNP-A capable of detecting UPD can offer more diagnostic and prognostic information; TP53 and RUNX1 gene mutations are often accompanied by abnormalities in their chromosomes (17p, 22q).
Keyphrases
  • genome wide
  • high density
  • transcription factor
  • high throughput
  • high resolution
  • healthcare
  • gene expression
  • mass spectrometry
  • dna methylation