Page 77 - FINAL PROGRAM
P. 77
TUESDAY, 5 JULY 2016
10:00 - 11:30 Hall 3 AB
Session 33: Deep sequencing the embryo
10:00 O-117
10:15 O-118
10:30 O-119
10:45 O-120
11:00 O-121
11:15 O-122
Quanti cation of low frequency variants of the mitochondrial DNA (mtDNA) in single cells by massive parallel sequencing (MPS)
F. Zambelli (Italy)
Design, validation and clinical application of a novel next-generation sequencing protocol for detection of mitochondrial disease and simultaneous aneuploidy screening in preimplantation embryos
K. Spath (United Kingdom)
Mitochondrial quanti cation during human embryogenesis via Next-generation sequencing: Relation to nuclear ploidy status
N. Arrach (U.S.A.)
The impact of simultaneous mitochondrial DNA (mtDNA) content assessment in comprehensive chromosomal screening (CCS): a prospective pilot study
F.K. Boynukalin (Turkey)
RNA-Seq reveals distinct transcriptomes in normal and trisomic human pre-implantation embryos
F. Licciardi (U.S.A.)
Selecting single blastocysts for transfer with next-generation sequencing signi cantly improves ongoing pregnancy rates for IVF patients: results from a randomized pilot study Z. Yang (U.S.A.)
FINAL PROGRAMME I HELSINKI, FINLAND – 3 TO 6 JULY 2016 73
SCIENTIFIC PROGRAMME TUESDAY, 5 JULY
