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相关概念视频

Maxam-Gilbert Sequencing01:05

Maxam-Gilbert Sequencing

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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...
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Next-generation Sequencing03:00

Next-generation Sequencing

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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....
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Sanger Sequencing01:57

Sanger Sequencing

757.7K
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...
757.7K
The Evidence for Evolution02:55

The Evidence for Evolution

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Genetic variations accumulating within populations over generations give rise to biological evolution. Evolutionary changes can result in the formation of novel varieties and entire new species. These changes are responsible for the diverse forms of life inhabiting the planet. The evidence for evolution suggests that all living organisms descended from common ancestors.
44.1K
RNA-seq03:21

RNA-seq

10.4K
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...
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Multi-species Conserved Sequences02:51

Multi-species Conserved Sequences

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Next-generation sequencing technologies have created large genomic databases of a variety of animals and plants. Ever since the human genome project was completed, scientists studied the genome of primates, mammals, and other phylogenetically distant living beings. Such large-scale  studies have provided new insights into the evolutionary relationship between organisms.
Although the genome of each species varies greatly from each other, a few sequences are highly conserved. Such conserved...
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相关实验视频

Updated: Sep 17, 2025

Novel Sequence Discovery by Subtractive Genomics
09:40

Novel Sequence Discovery by Subtractive Genomics

Published on: January 25, 2019

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测序证据

Margaux Quiniou1,2, Sebastian Jessberger1,2,3

  • 1Laboratory of Neural Plasticity, Faculties of Medicine and Science, Brain Research Institute, University of Zurich, Zurich, Switzerland.

Science (New York, N.Y.)
|July 3, 2025
PubMed
概括

研究人员使用先进的转录组分析在成年人海马体中发现神经前代细胞. 这一发现揭示了大脑的再生能力.

科学领域:

  • 神经科学
  • 细胞生物学
  • 基因组学

背景情况:

  • 长期以来人们认为成年人的大脑产生新神经元的能力有限.
  • 了解神经发生的细胞机制对于再生医学至关重要.

研究的目的:

  • 识别和描述成年人海马中的神经前代细胞.
  • 调查成年人大脑中神经发生的可能性.

主要方法:

  • 对海马组织样本的转录组分析.
  • 一个单细胞RNA测序.
  • 对基因表达数据的生物信息分析.

主要成果:

  • 在成年人海马体中识别出独特的神经前代细胞群.
  • 这些祖细胞的独特基因表达特征.
  • 支持成年人大脑中神经发生的证据.

结论:

  • 大人的海马体内存在神经前代细胞.
  • 这些细胞具有内生修复机制的潜力.
  • 这些发现挑战了关于成年人脑的有限神经生成能力的先前看法.

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Last Updated: Sep 17, 2025

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Novel Sequence Discovery by Subtractive Genomics

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