Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Accept all cookies' we'll assume that you are happy to receive all cookies and you won't see this message again. If you click 'Reject all non-essential cookies' only necessary cookies providing core functionality such as security, network management, and accessibility will be enabled. Click 'Find out more' for information on how to change your cookie settings.

Jonathan Campbell (13:00 - 13:30)

Title: Digital phenotyping of faces for rare diseases

Abstract: TBC

 

Munuse Savash (13:30 - 14:00)

Title: Precise quantification of DNA in spent culture media and its correlation to embryonic ploidy status

Abstract: Preimplantation genetic testing is a valuable tool for determining the genetic status of IVF embryos. However, the requirement for embryo biopsy necessitates specialist equipment and highly trained staff, substantially increasing costs. Additionally, there have been concerns that biopsy might risk damage to the embryo. We set out to provide the first accurate measurement of the amount of DNA in spent culture medium, and to gain an insight into why non-invasive PGT (niPGT) is less accurate than biopsy-based methods. We assessed spent media samples that underwent whole genome amplification via a novel quantitative PCR method. There was no difference in DNA quantity in media samples associated with euploid and aneuploid embryos. However, drops that held embryos until day-6 had significantly higher levels of DNA than those associated with culture to day-5 (P<0.0001). It has been hypothesised that the quantity of DNA in the medium may be predictive of the chromosomal status of an embryo. However, we found no evidence to support this notion. The amount of DNA in the medium increased with longer exposure to embryos, explaining why niPGT has higher reported accuracy when culture is extended beyond day-5.