一个DNA条形码术语词汇表
Miguel Vences1, Aurélien Miralles1,2, Robert DeSalle3
1Department of Evolutionary Biology, Zoological Institute, Technische Universität Braunschweig, Braunschweig, Germany.
Methods in molecular biology (Clifton, N.J.)
|April 29, 2024
概括
本词典定义了研究人员必需的DNA条形码术语. 它提供了清晰的定义,以帮助理解DNA条形码协议和应用.
科学领域:
- 遗传学 是一个遗传学.
- 分子生物学分子生物学
- 生物信息学是一种生物信息学.
背景情况:
- DNA 条形码是物种识别的关键方法.
- 标准化术语对于DNA条形码的可重复性研究至关重要.
研究的目的:
- 为提供关键DNA条形码术语的基础词汇表.
- 为本卷的读者澄清DNA条形码词典中的基本概念.
主要方法:
- 从DNA条形码词典中选择基本术语.
- 为每一个选定的术语制定清晰简洁的定义.
主要成果:
- 一个精心策划的基本DNA条形码术语词典.
- 可访问的定义,以促进对DNA条形码协议的理解.
结论:
- 该词汇表作为一个有价值的参考,研究人员新的DNA条形码.
- 标准化定义提高了DNA条形码领域的清晰度和一致性.
相关概念视频
Labeling DNA Probes
8.2K
DNA probes are fragments of DNA labeled with a reporter tag to enable their detection or purification. The resulting labeled DNA probes can then hybridize to target nucleic acid sequences through complementary base-pairing, and may be used to recover or identify these regions.
Radioisotopes, fluorophores, or small molecule binding partners like biotin or digoxigenin, are the most widely used reporter tags for labeling DNA probes. These labels can be attached to the probe DNA molecule via...
Radioisotopes, fluorophores, or small molecule binding partners like biotin or digoxigenin, are the most widely used reporter tags for labeling DNA probes. These labels can be attached to the probe DNA molecule via...
8.2K
Complementary DNA
29.5K
Overview
29.5K
Genome Annotation and Assembly
18.8K
The genome refers to all of the genetic material in an organism. It can range from a few million base pairs in microbial cells to several billion base pairs in many eukaryotic organisms. Genome assembly refers to the process of taking the DNA sequencing data and putting it all back together in a correct order to create a close representation of the original genome. This is followed by the identification of functional elements on the newly assembled genome, a process called genome annotation.
18.8K
Next-generation Sequencing
88.7K
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....
88.7K
DNA Microarrays
17.3K
Microarrays are high-throughput and relatively inexpensive assays that can be automated to analyze large quantities of data at a time. They are used in genome-wide studies to compare gene or protein expression under two varied conditions, such as healthy and diseased states. Microarrays consist of glass or silica slides on which probe molecules are covalently attached through surface functionalization. Most commonly, the slides are prepared through the chemisorption of silanes to silica...
17.3K
Sanger Sequencing
754.1K
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...
754.1K


