Introducing WISECONDOR for noninvasive prenatal diagnostics

Expert Rev Mol Diagn. 2014 Jun;14(5):513-5. doi: 10.1586/14737159.2014.919855. Epub 2014 May 16.

Abstract

Noninvasive prenatal testing is a relatively new screening method for the detection of fetal chromosome abnormalities using next-generation sequencing (NGS) of fetal DNA in maternal blood. Recently, the introduction of a new tool called WIthin SamplE COpy Number aberration DetectOR (WISECONDOR) marked a new era in prenatal screening. WISECONDOR detects copy number aberrations at a resolution that is almost comparable to classic karyotyping and requires only shallow sequencing, making noninvasive prenatal screening cost-effective. This emphasizes the role of NGS in the daily clinical practice of prenatal diagnosis and will require reorganization of clinical genetics laboratories to accommodate NGS. For prenatal diagnostics, WISECONDOR introduces an exciting development that will substantially improve the information provided to pregnant couples regarding their fetus's wellbeing.

Keywords: chromosomal aberrations; clinical practice; fetal DNA; next generation sequencing; noninvasive prenatal diagnostics.

Publication types

  • Review

MeSH terms

  • Chromosome Aberrations
  • Chromosome Disorders / diagnosis*
  • Chromosome Disorders / genetics
  • Female
  • High-Throughput Nucleotide Sequencing
  • Humans
  • Maternal Serum Screening Tests / methods*
  • Pregnancy
  • Sequence Analysis, DNA / methods*