生物
遗传学
队列
遗传咨询
全基因组测序
基因组
表型
DNA测序
计算生物学
基因组学
基因检测
医学
生物信息学
遗传变异
人类基因组
全基因组关联研究
产量(工程)
外显子组测序
染色体
遗传变异
人类遗传学
鉴定(生物学)
进化生物学
作者
Lijuan Pan,Jiayu Wu,Yi Zhang,Desheng Liang,Jing Yuan,Jue Wang,Yinchen Shen,Junjie Lu,Aihua Xia,Zhenhui Zhang,Jinchen Li,Zhuo Li,Lingqian Wu
摘要
OBJECTIVE: This study aimed to evaluate the detection rates of aneuploidies and pathogenic/likely pathogenic copy number variations (pCNV) using low-pass genome sequencing (LP-GS), also known as CNV-seq, across different ultrasonographic anomalies and to systematically elucidate the associations between specific types of chromosomal aberrations and specific ultrasonographic anomalies. METHOD: LP-GS was performed in 19,452 fetuses, including those with ultrasonographic anomalies (n = 13,312) and those with normal ultrasonography (n = 6140). The detection rates of pCNV among fetuses with various ultrasonographic anomalies were compared with those of fetuses with no identifiable anomalies. In addition, the associations between ultrasonographic anomalies and aneuploidies or pCNV were investigated using Fisher's exact test. RESULTS: The detection rates of aneuploidies and pCNV were 6.20% (825/13,312) and 6.19% (824/13,312), respectively, in fetuses with ultrasonographic anomalies. Fetal hydrops was the ultrasonographic anomaly with the highest diagnostic rate for aneuploidies, at 32.58% among all isolated groups, particularly when combined with cystic hygroma, for which the diagnostic rate was 61.04%. Ten types of isolated ultrasonographic anomalies showed significantly higher diagnostic rates of pCNV (3.90%-7.43%, p < 0.05, odds ratio = 2.19-4.32). Furthermore, this study first reported an association between 3q25.2-q29 duplication and abdominal wall defects. CONCLUSIONS: Our findings expanded the phenotypic spectrum of certain pCNVs and highlighted phenotype-specific differences in the diagnostic yield of LP-GS, providing valuable reference information for genetic counseling in prenatal diagnosis.
科研通智能强力驱动
Strongly Powered by AbleSci AI