Literature DB >> 24831532

Introducing WISECONDOR for noninvasive prenatal diagnostics.

Roy Straver1, Erik A Sistermans, Marcel J T Reinders.   

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.

Entities:  

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

Mesh:

Year:  2014        PMID: 24831532     DOI: 10.1586/14737159.2014.919855

Source DB:  PubMed          Journal:  Expert Rev Mol Diagn        ISSN: 1473-7159            Impact factor:   5.225


  7 in total

1.  Prenatal DNA Sequencing for Fetal Aneuploidy Also Detects Maternal Cancer: Importance of Timely Workup and Management in Pregnant Women.

Authors:  Amy E Turriff; Christina M Annunziata; Diana W Bianchi
Journal:  J Clin Oncol       Date:  2022-06-15       Impact factor: 50.717

2.  Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening.

Authors:  Wybo Dondorp; Guido de Wert; Yvonne Bombard; Diana W Bianchi; Carsten Bergmann; Pascal Borry; Lyn S Chitty; Florence Fellmann; Francesca Forzano; Alison Hall; Lidewij Henneman; Heidi C Howard; Anneke Lucassen; Kelly Ormond; Borut Peterlin; Dragica Radojkovic; Wolf Rogowski; Maria Soller; Aad Tibben; Lisbeth Tranebjærg; Carla G van El; Martina C Cornel
Journal:  Eur J Hum Genet       Date:  2015-03-18       Impact factor: 4.246

Review 3.  Non-invasive prenatal testing for fetal chromosome abnormalities: review of clinical and ethical issues.

Authors:  Jean Gekas; Sylvie Langlois; Vardit Ravitsky; François Audibert; David Gradus van den Berg; Hazar Haidar; François Rousseau
Journal:  Appl Clin Genet       Date:  2016-02-04

4.  Implementation of non-invasive prenatal testing by semiconductor sequencing in a genetic laboratory.

Authors:  Annelies Dheedene; Tom Sante; Matthias De Smet; Jean-François Vanbellinghen; Bernard Grisart; Sarah Vergult; Sandra Janssens; Björn Menten
Journal:  Prenat Diagn       Date:  2016-07-01       Impact factor: 3.050

5.  Comparative evaluation of the Minimally-Invasive Karyotyping (MINK) algorithm for non-invasive prenatal testing.

Authors:  Tianjiao Chu; Patricia A Shaw; Suveyda Yeniterzi; Mary Dunkel; Aleksander Rajkovic; W Allen Hogge; Kimberly D Bunce; David G Peters
Journal:  PLoS One       Date:  2017-03-17       Impact factor: 3.240

6.  Incidental finding of maternal malignancy in an unusual non-invasive prenatal test and a review of similar cases.

Authors:  Maria Hammer Moellgaard; Ida Charlotte Bay Lund; Naja Becher; Anne-Bine Skytte; Lotte Andreasen; Malgorzata Ilona Srebniak; Ida Vogel
Journal:  Clin Case Rep       Date:  2022-10-11

7.  Clinical utility of non-invasive prenatal testing in pregnancies with ultrasound anomalies.

Authors:  L Beulen; B H W Faas; I Feenstra; J M G van Vugt; M N Bekker
Journal:  Ultrasound Obstet Gynecol       Date:  2017-06       Impact factor: 7.299

  7 in total

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