短读基因组测序在产前诊断中的进展,挑战和前景
Yanfei Wang1, Xiaofan Zhu1, Zhi Gao1
1Genetics and Prenatal Diagnosis Center, Department of Obstetrics and Gynecology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Birth defects research
|August 20, 2025
概括
全基因组测序 (WGS) 显示出孕前诊断的前景,改善了胎儿异常的检测率. 然而,像不确定意义的变体这样的挑战在广泛临床使用之前需要进一步的研究.
科学领域:
- 遗传学
- 产前医学
- 基因组技术
背景情况:
- 全基因组测序 (WGS) 越来越多地被用于临床遗传测试.
- 它在产前诊断中的应用是一个不断增长的研究领域.
- 初步验证支持WGS的临床实用性.
研究的目的:
- 审查目前关于产前诊断的WGS研究和指导方针.
- 介绍WGS在产前环境中的方法,范围和诊断能力.
- 讨论临床有用性,可行性,局限性和道德考虑.
主要方法:
- 对现有文献和指导方针进行系统审查.
- 在产前诊断中WGS应用的分析.
- 对诊断率,实用性和挑战的综合数据.
主要成果:
- WGS显示有可能提高发育异常的胎儿的诊断率.
- 增加不确定的变异的检测是一个重大挑战.
- 证据表明WGS可以提高产前诊断产量.
结论:
- 全基因组测序具有很大的潜力来推进产前诊断.
- 为了克服目前的局限性并促进临床整合,进一步的研究至关重要.
- 需要继续调查以优化产前应用的WGS协议和解释.
相关概念视频
Next-generation Sequencing
92.5K
The first human genome sequencing project cost $2.7 billion and was declared complete in 2003, after 15 years of international cooperation and collaboration between several research teams and funding agencies. Today, with the advent of next-generation sequencing technologies, the cost and time of sequencing a human genome have dropped over 100 fold.
Next-Generation Sequencing Methods
Although all next-generation methods use different technologies, they all share a set of standard features....
Next-Generation Sequencing Methods
Although all next-generation methods use different technologies, they all share a set of standard features....
92.5K
Sanger Sequencing
756.9K
DNA sequencing is a fundamental technique that is routinely used in the biological sciences. This method can be applied to a range of questions at different scales - from the sequencing of a cloned DNA fragment or the study of a mutation in a gene up to whole-genome sequencing. However, despite the widespread use of sequencing today, it was not until 1977 that Fredrick Sanger and his collaborators developed the chain-termination method to decode DNA sequences. It relies on the separation of a...
756.9K
Maxam-Gilbert Sequencing
11.4K
In the same year as the discovery of the Sanger sequencing method, another group of scientists, Allan Maxam and Walter Gilbert, demonstrated their chemical-cleavage method for DNA sequencing. The Maxam-Gilbert method relies on using different chemicals that can cleave the DNA sequence at specific sites, the separation of resulting DNA fragments of variable size using electrophoresis, and deciphering the DNA sequence from the resulting gel bands.
Challenges of the Maxam-Gilbert Method
The...
Challenges of the Maxam-Gilbert Method
The...
11.4K
Genome Annotation and Assembly
19.3K
The genome refers to all of the genetic material in an organism. It can range from a few million base pairs in microbial cells to several billion base pairs in many eukaryotic organisms. Genome assembly refers to the process of taking the DNA sequencing data and putting it all back together in a correct order to create a close representation of the original genome. This is followed by the identification of functional elements on the newly assembled genome, a process called genome annotation.
19.3K
Genomics
37.4K
Genomics is the science of genomes: it is the study of all the genetic material of an organism. In humans, the genome consists of information carried in 23 pairs of chromosomes in the nucleus, as well as mitochondrial DNA. In genomics, both coding and non-coding DNA is sequenced and analyzed. Genomics allows a better understanding of all living things, their evolution, and their diversity. It has a myriad of uses: for example, to build phylogenetic trees, to improve productivity and...
37.4K


