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Updated: Sep 12, 2025

A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations
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利用下一代测序来探索短根异常的分子病因学

Emily A Joy1, David K Crossman2, Mary MacDougall3

  • 1Department of Orthodontics, School of Dentistry, University of Alabama at Birmingham, Birmingham, Alabama, USA.

Orthodontics & craniofacial research
|August 9, 2025
PubMed
概括

H1C基因的突变与自体主导短根异常 (SRA) 相关,SRA是一种影响牙根发育的遗传牙科疾病. 这一发现揭示了西班牙裔家庭SRA的分子原因.

关键词:
遗传模式是一种遗传模式.根的形成 根的形成短根异常短根异常整体外基因组测序H1C

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Next-generation Sequencing03:00

Next-generation Sequencing

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....
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