Comment on "Noninvasive prenatal screening at low fetal fraction: comparing whole-genome sequencing and single-nucleotide polymorphism methods"

Prenat Diagn. 2017 Jul;37(7):725-726. doi: 10.1002/pd.5072.
No abstract available

Publication types

  • Letter
  • Comment

MeSH terms

  • DNA
  • Female
  • Fetus*
  • High-Throughput Nucleotide Sequencing
  • Humans
  • Nucleotides
  • Polymorphism, Single Nucleotide
  • Pregnancy
  • Prenatal Diagnosis*
  • Sequence Analysis, DNA

Substances

  • Nucleotides
  • DNA