Reproducibility of different aneuploid findings at second trophectoderm biopsy evaluated by independent NGS platforms

Horák, Jakub; Kubicek, David; Navratil, Rostislav; Horňák, Miroslav; Janíčková, N.; Tauwinklova, Gabriela; Veselá, Kateřina

doi:10.1016/j.rbmo.2019.03.030

Cited by 1 publication

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“…However, additional family members are needed to infer the parental haplotype to identify balanced translocations and monogenic mutations in the tested embryos. A recently described PGT protocol called OneGene PGT allows direct mutation testing, haplotyping and aneuploidy screening via next-generation sequencing (NGS) (Hornak et al, 2023). The whole-genome amplification product was combined with multiplex PCR for SNP enrichment.…”

Section: Introductionmentioning

confidence: 99%

Proband-independent haplotyping based on NGS-based long-read sequencing for detecting pathogenic variant carrier status in preimplantation genetic testing for monogenic diseases

Zhang,

Zhao,

et al. 2024

Front. Mol. Biosci.

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Preimplantation genetic testing for monogenic diseases (PGT-M) can be used to select embryos that do not develop disease phenotypes or carry disease-causing genes for implantation into the mother’s uterus, to block disease transmission to the offspring, and to increase the birth rate of healthy newborns. However, the traditional PGT-M technique has some limitations, such as its time consumption, experimental procedural complexity, and the need for a complete family or reference embryo to construct the haplotype. In this study, proband-independent haplotyping based on NGS-based long-read sequencing (Phbol-seq) was used to effectively construct haplotypes. By targeting the mutation sites of single gene disease point mutations and small fragment deletion carriers, embryos carrying parental disease-causing mutations were successfully identified by linkage analysis. The efficiency of embryo resolution was then verified by classical Sanger sequencing, and it was confirmed that the construction of haplotype and SNP linkage analysis by Phbol-seq could accurately and effectively detect whether embryos carried parental pathogenic mutations. After the embryos confirmed to be nonpathogenic by Phbol-seq-based PGT-M and confirmed to have normal copy number variation by Phbol-seq-based PGT-A were transplanted into the uterus, gene detection in amniotic fluid of the implanted embryos was performed, and the results confirmed that Phbol-seq technology could accurately distinguish normal genotype embryos from genetically modified carrier embryos. Our results suggest that Phbol-seq is an effective strategy for accurately locating mutation sites and accurately distinguishing between embryos that inherit disease-causing genes and normal embryos that do not. This is critical for Phbol-seq-based PGT-M and could help more single-gene disease carriers with incomplete families, de novo mutations or suspected germline mosaicism to have healthy babies with normal phenotypes. It also helps to reduce the transmission of monogenic genetic diseases in the population.

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Section: Introductionmentioning

confidence: 99%