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Next-generation Sequencing03:00

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....
88.7K
Sanger Sequencing01:57

Sanger Sequencing

754.2K
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...
754.2K
DNA as a Genetic Template02:05

DNA as a Genetic Template

21.9K
Two structural features of the DNA molecule provide a basis for the mechanisms of heredity: the four nucleotide bases and its double-stranded nature. The Watson-Crick model of double-helical DNA structure, proposed in 1952, drew heavily upon the X-ray crystallography work of researchers Rosalind Franklin and Maurice Wilkins. Watson, Crick, and Wilkins jointly received the Nobel Prize in Physiology or Medicine for their work in 1962. Franklin was, controversially, excluded from the prize for...
21.9K
RNA-seq03:21

RNA-seq

9.9K
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...
9.9K
Maxam-Gilbert Sequencing01:05

Maxam-Gilbert Sequencing

11.2K
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...
11.2K
The DNA Helix01:16

The DNA Helix

139.7K
Overview
139.7K

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相关实验视频

Updated: Jun 29, 2025

Sequencing of mRNA from Whole Blood using Nanopore Sequencing
11:26

Sequencing of mRNA from Whole Blood using Nanopore Sequencing

Published on: June 3, 2019

13.7K

连锁的纳米孔DNA代码

Adrian Vidal, V B Wijekoon, Emanuele Viterbo

    IEEE transactions on nanobioscience
    |March 28, 2024
    PubMed
    概括

    研究人员开发了一种新的DNA代码构造方法,用于纳米孔测序数据存储. 这种方法通过连接DNA k-mers来提高数据对测序错误的稳定性,提高存储效率和解码复杂性.

    科学领域:

    • 生物信息学是一种生物信息学.
    • 分子工程分子工程分子工程
    • 数据存储数据存储数据存储

    背景情况:

    • 纳米孔测序产生杂的DNA信号.
    • 存储DNA数据需要强大的代码来防止测序错误.
    • 目前的代码设计方法受到图形复杂性的限制.

    研究的目的:

    • 开发一种强大的DNA代码结构,用于纳米孔测序.
    • 为了提高DNA数据存储的存储效率和解码.
    • 在纳米孔测序中减轻噪声和通道记忆效应.

    主要方法:

    • 从基基DNA代码中连接密码.
    • 在基础代码中加入一个环接字来减少频道内存.
    • 通过模拟分析解码复杂性和错误率.

    主要成果:

    • 通过连接k-mers来构建大型DNA代码.
    • 随着连接k-mers的增加,已证明稳定的基准代码错误率.
    • 显示解码复杂度尺度与连接k-mers的数量.

    结论:

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    相关实验视频

    Last Updated: Jun 29, 2025

    Sequencing of mRNA from Whole Blood using Nanopore Sequencing
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    Sequencing of mRNA from Whole Blood using Nanopore Sequencing

    Published on: June 3, 2019

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    Ultra-long Read Sequencing for Whole Genomic DNA Analysis
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    Ultra-long Read Sequencing for Whole Genomic DNA Analysis

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    Nanopore DNA Sequencing for Metagenomic Soil Analysis

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  • 连锁提供了一个可扩展的方法来构建强大的DNA代码.
  • 环形补丁有助于减少纳米孔通道记忆效应.
  • 这种方法提高了基于DNA的数据存储的实用性.