相关实验视频
Updated: Jun 11, 2025

08:38
Targeted DNA Methylation Analysis by Next-generation Sequencing
Published on: February 24, 2015
37.0K
DNAMarkMaker:简化了ARMS和CAPS标记器的开发,通过NGS短读重序列数据来简化标记器的开发
Tenta Segawa1, Sorachi Saiga1, Marina Takata1
1Ishikawa Prefectural University, 1-308 Suematsu, Nonoichi, Ishikawa 921-8836, Japan.
Breeding science
|October 2, 2024
概括
DNAMarkMaker自动化了用于放大阻抗突变系统 (ARMS) 和切割放大多态序列 (CAPS) 标记物的DNA标记器开发. 这种工具通过简化原料设计来加速遗传分析和作物育种.
科学领域:
- 植物遗传学 植物遗传学
- 生物信息学是一种生物信息学.
- 分子育种是一种分子育种.
背景情况:
- DNA标记物对于作物育种和遗传分析至关重要.
- 开发DNA标记物通常是耗时和劳动密集的,需要多形态识别和原始设计.
研究的目的:
- 开发DNAMarkMaker,这是一个自动化工具,用于设计ARMS和CAPSDNA标记器的原料.
- 通过重新测序数据简化DNA标记物开发过程.
主要方法:
- 开发了DNAMarkMaker,具有用户友好的图形用户界面 (GUI).
- 利用再测序数据进行自动化初始设计.
- 在具有多样化基因组结构的米,土豆和卜上测试了该工具.
主要成果:
- DNAMarkMaker成功自动化了ARMS和CAPS标记器的初始设计.
- 该工具证明了在不同植物物种和种植水平上适用性.
- 促进了 homozygous diploid, heterozygous autotetraploid 和 heterozygous diploid 基因组的标志物开发. 这种基因组可以分为两种类型.
结论:
- DNAMarkMaker显著加速了DNA标记物的开发.
- 该工具提高了作物育种和遗传分析的效率.
- DNAMarkMaker可供具有不同生物信息学专业知识的研究人员访问.
更多相关视频
13:24Integration of Wet and Dry Bench Processes Optimizes Targeted Next-generation Sequencing of Low-quality and Low-quantity Tumor Biopsies
Published on: April 11, 2016
11.8K
06:40G2-seq: A High Throughput Sequencing-based Technique for Identifying Late Replicating Regions of the Genome
Published on: March 22, 2018
5.8K
相关概念视频
Next-generation Sequencing
88.4K
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....
88.4K
RNA-seq
9.8K
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...
9.8K
Sanger Sequencing
753.8K
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...
753.8K