Comprehensive application of multiple molecular diagnostic techniques in pre-implantation genetic testing for monogenic.
Peng HuangYueyun LanHong ZhouLuye LinJinhui ShuCaizhu WangXin ZhaoLifang LiangSheng HeJingfei MouXiaofei ZhangQingming QiuHongwei WeiPublished in: Molecular genetics & genomic medicine (2023)
In conclusion, this study found that SNP analysis is advantageous for identifying polygenic and deletional mutations, whereas NGS is more cost-efficient for detecting common monogenic diseases. Additionally, SNP-based haplotyping and PCR-based direct detection of mutations can be used together to enhance the accuracy and success rates of PGT-M. Our findings offer valuable insights for PGT technicians in choosing suitable detection methods for patients.