相关实验视频
Updated: Jan 10, 2026

10:34
Ultra-long Read Sequencing for Whole Genomic DNA Analysis
Published on: March 15, 2019
23.9K
化保存高分子量本地DNA用于临床长读序列测序
medRxiv : the preprint server for health sciences
|November 24, 2025
概括
化是一种新的DNA保存方法,在环境温度下保持长时间读取的测序质量. 这种技术消除了对冷链基础设施的需求,使先进的基因组学在全球范围内可用.
科学领域:
- 基因组学就是基因组学.
- 分子生物学分子生物学
- 生物技术是生物技术.
背景情况:
- 长时间读取的DNA测序可以同时检测遗传变异和表观遗传修饰.
- 目前的保存方法需要冷链基础设施,限制资源有限的环境和现场研究中的可访问性.
研究的目的:
- 评估化作为一种在环境温度下维护DNA完整性和测序性能的方法.
- 在真实世界患者样本中证明化DNA对诊断质量的长读测序的实用性.
主要方法:
- DNA样本被封装在二氧化矩阵 (化) 中.
- 化DNA经过环境温度储存,处理和加速气候变化测试.
- 化DNA的测序性能与使用基因组在瓶子 (GIAB) 参考样本的冷对照进行了比较.
- 化患者样本进行了本地长读测序,以进行变异和甲基化分析.
主要成果:
- 化保持了DNA完整性,与在环境温度下冷至-80°C相比.
- 化DNA保持了测序性能,并在模拟的长期存储和处理中表现出对降解的抵抗力.
- 化患者样本的原生长读测序成功识别出了de novo变种和诊断甲基化表征.
结论:
- 化有效地保存DNA,用于具有诊断质量的长读测序,无需冷链要求.
- 这种方法显著扩大了在资源有限的环境和现场应用中使用先进的基因组技术的机会.
相关概念视频
Sanger Sequencing
772.9K
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...
772.9K
Next-generation Sequencing
97.6K
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....
97.6K
RNA-seq
11.7K
RNA sequencing, or RNA-Seq, is a high-throughput sequencing technology used to study the transcriptome of a cell. Transcriptomics helps to interpret the functional elements of a genome and identify the molecular constituents of an organism. Additionally, it also helps in understanding the development of an organism and the occurrence of diseases.
Before the discovery of RNA-seq, microarray-based methods and Sanger sequencing were used for transcriptome analysis. However, while...
Before the discovery of RNA-seq, microarray-based methods and Sanger sequencing were used for transcriptome analysis. However, while...
11.7K
DNA Isolation
44.4K
DNA isolation protocols can be fast and straightforward or complex and time-consuming depending on the type and quality of DNA required for further processing. For example, plasmid DNA extraction is a bit more complicated than genomic DNA extraction because of the need for an appropriate lysis method to separate plasmid DNA from gDNA during isolation. However, for specific applications, such as long-range DNA sequencing that require a good yield of high- quality DNA samples, we need to follow...
44.4K
Maxam-Gilbert Sequencing
12.6K
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...
12.6K

