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Related Concept Videos

RNA-seq03:21

RNA-seq

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 microarray-based...
Next-generation Sequencing03:00

Next-generation Sequencing

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.
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Sanger Sequencing

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Maxam-Gilbert Sequencing01:05

Maxam-Gilbert Sequencing

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.
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Related Experiment Video

Updated: May 20, 2026

Enhanced Reduced Representation Bisulfite Sequencing for Assessment of DNA Methylation at Base Pair Resolution
13:47

Enhanced Reduced Representation Bisulfite Sequencing for Assessment of DNA Methylation at Base Pair Resolution

Published on: February 24, 2015

High-throughput sequencing of the methylome using two-base encoding.

Christina A Bormann Chung1

  • 1Life Technologies, Foster City, CA, USA. Christina.Chung@lifetech.com

Methods in Molecular Biology (Clifton, N.J.)
|July 24, 2012
PubMed
Summary
This summary is machine-generated.

Studying DNA methylation patterns is crucial for understanding cell development and diseases like cancer. This research introduces a new method using bisulfite sequencing and SOLiD technology for precise methylome analysis.

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Related Experiment Videos

Last Updated: May 20, 2026

Enhanced Reduced Representation Bisulfite Sequencing for Assessment of DNA Methylation at Base Pair Resolution
13:47

Enhanced Reduced Representation Bisulfite Sequencing for Assessment of DNA Methylation at Base Pair Resolution

Published on: February 24, 2015

Methyl-binding DNA capture Sequencing for Patient Tissues
08:40

Methyl-binding DNA capture Sequencing for Patient Tissues

Published on: October 31, 2016

Targeted DNA Methylation Analysis by Next-generation Sequencing
08:38

Targeted DNA Methylation Analysis by Next-generation Sequencing

Published on: February 24, 2015

Area of Science:

  • Epigenetics and Molecular Biology
  • Genomics and Bioinformatics

Background:

  • Epigenetic modifications, including DNA methylation, are critical for cellular regulation in both health and disease.
  • Altered methylation patterns are linked to various conditions such as cancer, neurodevelopmental, and endocrine disorders.

Purpose of the Study:

  • To describe a novel method for analyzing the methylome at single-base resolution.
  • To enhance the understanding of epigenetic regulation in disease development.

Main Methods:

  • Utilized bisulfite sequencing to detect methylation.
  • Combined bisulfite sequencing with high-throughput SOLiD sequencing technology for methylome analysis.

Main Results:

  • Developed a method enabling single-base resolution of DNA methylation patterns.
  • Facilitated detailed study of the methylome.

Conclusions:

  • The described method provides valuable insights into the underlying causes of diseases by analyzing methylation patterns.
  • High-throughput sequencing technologies are powerful tools for epigenetic research.