校正:针对正常型和染色体重组的非侵入性染色体查的有效性
Bo-Lan Sun1, Yong Wang1, Sixi Wen1
1The Reproductive Medicine Center, Peking University Shenzhen Hospital, Shenzhen, Guangdong, China.
Frontiers in genetics
|November 11, 2025
概括
这项研究纠正了先前发表的一篇文章. 校正确保了准确的引用和数据完整性,用于该领域未来的研究.
科学领域:
- 遗传学 遗传学 是一个
- 生物信息学是一种生物信息学.
背景情况:
- 以前的出版物需要更正.
- 确保科学准确性对于研究完整性至关重要.
研究的目的:
- 为了纠正某一特定出版物的文章DOI.
- 为了保持准确的引用和数据检索.
主要方法:
- 发出了一份正式的纠正通知.
- 文章的DOI在相关数据库中进行了更新.
主要成果:
- 文章DOI已经被纠正.
- 修正后的DOI确保了正确的归属和访问.
结论:
- 修正方便了准确的引用.
- 这确保了科学记录的完整性.
相关概念视频
Karyotyping
68.0K
Overview
68.0K
Genetic Screens
5.6K
Genetic screens are tools used to identify genes and mutations responsible for phenotypes of interest. Genetic screens help identify individuals or a group of people at risk of developing genetic diseases and help them with early intervention, targeted therapy, and reproductive options.
Forward genetic screens
Forward or “classical” genetic screens involve creating random mutations in an organism’s DNA using radiation, mutagens, or insertion of additional bases, which...
Forward genetic screens
Forward or “classical” genetic screens involve creating random mutations in an organism’s DNA using radiation, mutagens, or insertion of additional bases, which...
5.6K


