Literature DB >> 31595440

BACs-on-Beads™ assay, a rapid aneuploidy test, improves the diagnostic yield of conventional karyotyping.

Chantal Farra1, Anwar H Nassar2, Fadi Mirza2, Lina Abdouni1, Mirna Souaid1, Johnny Awwad3,4.   

Abstract

BACs-on-Beads (BoBs™) assay is a rapid aneuploidy test (RAT) that detects numerical chromosomal aneuploidies and multiple microdeletion/microduplication syndromes. This study was conducted to appraise the usefulness of the BoB™ assay as a complementary diagnostic tool to conventional karyotyping for the rapid detection of chromosomal aneuploidies. A total of 485 prenatal (amniotic fluid and chorionic villi) and blood/products of conception samples were collected between July 2013 and August 2018, and analyzed by the BoBs™ assay and cytogenetic karyotyping and further validated by fluorescence in situ hybridization (FISH). Forty-three of 484 qualifying samples (8.9%) were identified as abnormal by the BoBs™ assay. The assay was comparable to karyotyping in the detection of common structural abnormalities (trisomy 21, trisomy 18, X, and Y), with a sensitivity of 96.0% and a specificity of 100%. BoBs™ assay detected 20 microdeletion and microduplication syndromes that were missed by karyotyping. BoBs™, however, missed 10 cases of polyploidies and chromosomal rearrangements which were identified by conventional karyotyping. Our findings suggest that BoBs™ is a reliable RAT which is suitable in combination with conventional karyotyping for the detection of common aneuploidies. The assay also improves the diagnostic yield by recognizing clinically relevant submicroscopic copy number gains and losses.

Entities:  

Keywords:  Aneuploidies; BACs-on-Beads™; Karyotype; Microdeletions; Microduplications

Mesh:

Year:  2019        PMID: 31595440     DOI: 10.1007/s11033-019-05117-7

Source DB:  PubMed          Journal:  Mol Biol Rep        ISSN: 0301-4851            Impact factor:   2.316


  27 in total

1.  Clinical application of multiplex quantitative fluorescent polymerase chain reaction (QF-PCR) for the rapid prenatal detection of common chromosome aneuploidies.

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Journal:  Mol Hum Reprod       Date:  2001-10       Impact factor: 4.025

2.  Chromosome abnormalities investigated by non-invasive prenatal testing account for approximately 50% of fetal unbalances associated with relevant clinical phenotypes.

Authors:  Francesca Romana Grati; Andrea Barlocco; Beatrice Grimi; Silvia Milani; Giuditta Frascoli; Anna Maria Di Meco; Rosaria Liuti; Anna Trotta; Sara Chinetti; Francesca Dulcetti; Anna Maria Ruggeri; Simona De Toffol; Maurizio Clementi; Federico Maggi; Giuseppe Simoni
Journal:  Am J Med Genet A       Date:  2010-06       Impact factor: 2.802

Review 3.  The impact of human copy number variation on a new era of genetic testing.

Authors:  K W Choy; S R Setlur; C Lee; T K Lau
Journal:  BJOG       Date:  2010-01-26       Impact factor: 6.531

Review 4.  Rapid methods for targeted prenatal diagnosis of common chromosome aneuploidies.

Authors:  Brigitte H W Faas; Vincenzo Cirigliano; The-Hung Bui
Journal:  Semin Fetal Neonatal Med       Date:  2011-04       Impact factor: 3.926

5.  Rapid and novel prenatal molecular assay for detecting aneuploidies and microdeletion syndromes.

Authors:  Susan J Gross; Komal Bajaj; David Garry; Susan Klugman; Barry M Karpel; Anne Marie Roe; Brian J Wagner; Jenny Zhan; Stephen D Apfelroth; Nicole Schreiber-Agus
Journal:  Prenat Diagn       Date:  2011-01-04       Impact factor: 3.050

6.  Experience using a rapid assay for aneuploidy and microdeletion/microduplication detection in over 2,900 prenatal specimens.

Authors:  Jill A Rosenfeld; S Anne Morton; Cathryn Hummel; Scott G Sulpizio; Lisa D McDaniel; Roger A Schultz; Beth S Torchia; J Britt Ravnan; Jay W Ellison; Allan J Fisher
Journal:  Fetal Diagn Ther       Date:  2014-08-08       Impact factor: 2.587

Review 7.  Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies.

Authors:  David T Miller; Margaret P Adam; Swaroop Aradhya; Leslie G Biesecker; Arthur R Brothman; Nigel P Carter; Deanna M Church; John A Crolla; Evan E Eichler; Charles J Epstein; W Andrew Faucett; Lars Feuk; Jan M Friedman; Ada Hamosh; Laird Jackson; Erin B Kaminsky; Klaas Kok; Ian D Krantz; Robert M Kuhn; Charles Lee; James M Ostell; Carla Rosenberg; Stephen W Scherer; Nancy B Spinner; Dimitri J Stavropoulos; James H Tepperberg; Erik C Thorland; Joris R Vermeesch; Darrel J Waggoner; Michael S Watson; Christa Lese Martin; David H Ledbetter
Journal:  Am J Hum Genet       Date:  2010-05-14       Impact factor: 11.025

8.  The development of a rapid assay for prenatal testing of common aneuploidies and microdeletion syndromes.

Authors:  Lisa G Shaffer; Justine Coppinger; S Annie Morton; Sarah Alliman; Jessica Burleson; Ryan Traylor; Cathryn Walker; Steve Byerly; Allen N Lamb; Roger Schultz; J Britt Ravnan; Catherine D Kashork; Beth S Torchia; Scott Sulpizio; Kyle Sundin; Mack Schermer; Karl Adler; Stephanie Dallaire; Blake C Ballif
Journal:  Prenat Diagn       Date:  2011-06-21       Impact factor: 3.050

9.  Rapid aneuploidy detection with multiplex ligation-dependent probe amplification: a prospective study of 4000 amniotic fluid samples.

Authors:  Diane Van Opstal; Marjan Boter; Danielle de Jong; Cardi van den Berg; Hennie T Brüggenwirth; Hajo I J Wildschut; Annelies de Klein; Robert-Jan H Galjaard
Journal:  Eur J Hum Genet       Date:  2008-09-10       Impact factor: 4.246

10.  BACs-on-Beads technology: a reliable test for rapid detection of aneuploidies and microdeletions in prenatal diagnosis.

Authors:  Sandra García-Herrero; Inmaculada Campos-Galindo; José Antonio Martínez-Conejero; Vicente Serra; Inés Olmo; Coral Lara; Carlos Simón; Carmen Rubio
Journal:  Biomed Res Int       Date:  2014-03-27       Impact factor: 3.411

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  3 in total

1.  17p13.3 Microduplication Syndrome: Further Delineating the Clinical Spectrum.

Authors:  Chantal Farra; Lina Abdouni; Abeer Hani; Leyla Dirani; Layal Hamdar; Mirna Souaid; Johnny Awwad
Journal:  J Pediatr Genet       Date:  2020-07-20

2.  BACs-on-Beads Assay for the Prenatal Diagnosis of Microdeletion and Microduplication Syndromes.

Authors:  Chunyan Li; Jianfang Zhang; Jia Li; Guyuan Qiao; Ying Zhan; Ying Xu; Hong Yang
Journal:  Mol Diagn Ther       Date:  2021-04-07       Impact factor: 4.074

3.  Clinical Utility of the Prenatal BACs-on-Beads™ Assay in Invasive Prenatal Diagnosis.

Authors:  Yu Jiang; Lili Wu; Yunshen Ge; Jian Zhang; Yanru Huang; Qichang Wu; Yanhong Zhang; Yulin Zhou
Journal:  Front Genet       Date:  2022-01-14       Impact factor: 4.599

  3 in total

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