Karyomapping and how is it improving preimplantation genetics?

Gould, Rebecca L and Griffin, Darren K. (2017) Karyomapping and how is it improving preimplantation genetics? Expert Review of Molecular Diagnostics, . ISSN 1473-7159. E-ISSN 1744-8352. (doi:https://doi.org/10.1080/14737159.2017.1325736) (Access to this publication is currently restricted. You may be able to access a copy if URLs are provided)

PDF - Author's Accepted Manuscript
Restricted to Repository staff only until 28 April 2018.
Contact us about this Publication Download (1MB)
[img]
Official URL
https://doi.org/10.1080/14737159.2017.1325736

Abstract

Introduction: Preimplantation genetic diagnosis and screening (PGD/PGS) has been applied clinically for >25 years however inherent drawbacks include the necessity to tailor each case to the trait in question, and that technology to detect monogenic and chromosomal disorders respectively is fundamentally different. Areas Covered: The area of preimplantation genetics has evolved over the last 25 years, adapting to changes in technology and the need for more efficient, streamlined diagnoses. Karyomapping allows the determination of inheritance from the (grand)parental haplobocks through assembly of inherited chromosomal segments. The output displays homologous chromosomes, crossovers and the genetic status of the embryos by linkage comparison, as well as chromosomal disorders. It also allows for determination of heterozygous SNP calls, avoiding the risks of allele dropout, a common problem with other PGD techniques. Manuscripts documenting the evolution of preimplantation genetics, especially those investigating technologies that would simultaneously detect monogenic and chromosomal disorders, were selected for review. Expert Commentary: Karyomapping is currently available for detection of single gene disorders; ~1000 clinics worldwide offer it (via ~20 diagnostic laboratories) and ~2500 cases have been performed. Due an inability to detect post-zygotic trisomy reliably however and confounding problems of embryo mosaicism, karyomapping has yet to be applied clinically for detection of chromosome disorders.

Item Type: Article
Uncontrolled keywords: PGT, Karyomapping, PGD, PGS, IVF
Subjects: Q Science
Divisions: Faculties > Sciences > School of Biosciences
Depositing User: Sue Davies
Date Deposited: 02 May 2017 14:28 UTC
Last Modified: 15 May 2017 10:49 UTC
Resource URI: https://kar.kent.ac.uk/id/eprint/61593 (The current URI for this page, for reference purposes)
  • Depositors only (login required):

Downloads

Downloads per month over past year