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Updated: Jul 29, 2026

Array Comparative Genomic Hybridization Array CGH for Detection of Genomic Copy Number Variants
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Array Comparative Genomic Hybridization Array CGH for Detection of Genomic Copy Number Variants

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通过使用基于微阵列的比较基因组杂交来识别转移性口腔状癌患者的副本数交替概况:一项针对土耳其患者的研究

Meral Unur1, Zeynep Birsu Cincin2, Tuncay Tanıs3

  • 1Department of Oral Surgery and Medicine, Dental Faculty, Istanbul University, Istanbul, Turkey.

Journal of stomatology, oral and maxillofacial surgery
|August 2, 2023
PubMed
概括

鉴定了口腔状细胞癌 (OSCC) 的遗传变化,揭示了与转移相关的关键基因组变化. 这些发现可能会导致高级OSCC的新诊断生物标志物.

关键词:
在CNV中,CNV是NV.比较基因组杂交的基因组杂交.这是OSCCCC的OSCC.结构变化 结构变化

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相关概念视频

Comparing Copy Number Variations and SNPs02:26

Comparing Copy Number Variations and SNPs

Sequencing of the human genome has opened up several best-kept secrets of the genome. Scientists have identified thousands of genome variations that exist within a population. These variations can be a single nucleotide or a larger chromosomal variation.
Copy number variations or CNVs are the structural variations that cover more than 1kb of DNA sequence. The single nucleotide polymorphism (SNP), on the other hand, is a single nucleotide change or a point mutation that is found in more than 1%...