Result of Prospective Validation of the Trisomy Test(®) for the Detection of Chromosomal Trisomies

Samankaltaisia teoksia

• Copy Number Variant Detection with Low-Coverage Whole-Genome Sequencing Represents a Viable Alternative to the Conventional Array-CGH
  Tekijä: Kucharík, Marcel, et al.
  Julkaistu: (2021)
• Non-invasive prenatal testing (NIPT) by low coverage genomic sequencing: Detection limits of screened chromosomal microdeletions
  Tekijä: Kucharik, Marcel, et al.
  Julkaistu: (2020)
• Telomere length as a biomarker for fetal fraction prediction in non-invasive prenatal testing.
  Tekijä: Zuzana Holesova, et al.
  Julkaistu: (2025-01-01)
• Validation of Copy Number Variants Detection from Pregnant Plasma Using Low-Pass Whole-Genome Sequencing in Noninvasive Prenatal Testing-Like Settings
  Tekijä: Hyblova, Michaela, et al.
  Julkaistu: (2020)
• Utilization of Benchtop Next Generation Sequencing Platforms Ion Torrent PGM and MiSeq in Noninvasive Prenatal Testing for Chromosome 21 Trisomy and Testing of Impact of In Silico and Physical Size Selection on Its Analytical Performance.
  Tekijä: Gabriel Minarik, et al.
  Julkaistu: (2015-01-01)