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Updated: Jul 20, 2026

Next Generation Sequencing for the Detection of Actionable Mutations in Solid and Liquid Tumors
11:15

Next Generation Sequencing for the Detection of Actionable Mutations in Solid and Liquid Tumors

Published on: September 20, 2016

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精确检测复制数变化的关键参数,用于在甲固定型胺嵌入的固体癌症样本中精确检测复制数变化

Hanne Goris1,2, Vasiliki Siozopoulou2,3, Léon C van Kempen1,2,4

  • 1Department of Pathology, Antwerp University Hospital, Belgium.

Molecular oncology
|December 24, 2025
PubMed
概括

超低通全基因组测序 (ULP-WGS) 为癌症诊断中检测副本数变异 (CNV) 提供了一种可靠的方法. WisecondorX在临床使用方面表现有前途,在准确性方面表现优于SNP数组,并减少错误阳性.

关键词:
FFPE组织组织.这是一个SNP阵列阵列.在ULP-WGS中使用.癌症的诊断 癌症的诊断副本数量的变化 副本数量的变化

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Preparation of Formalin-fixed Paraffin-embedded Tissue Cores for both RNA and DNA Extraction08:30

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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%...