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Related Concept Videos

DNA Base Pairing02:27

DNA Base Pairing

Erwin Chargaff’s rules on DNA equivalence paved the way for the discovery of base pairing in DNA. Chargaff’s rules state that in a double-stranded DNA molecule,
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DNA Base Pairing02:27

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Sanger Sequencing

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...
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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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Maxam-Gilbert Sequencing01:05

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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.
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Related Experiment Video

Updated: Jun 19, 2026

DNA Methylation: Bisulphite Modification and Analysis
12:34

DNA Methylation: Bisulphite Modification and Analysis

Published on: October 21, 2011

Computational analysis of DNA methylation from long-read sequencing.

Yilei Fu1, Winston Timp2, Fritz J Sedlazeck3,4,5

  • 1Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX, USA.

Nature Reviews. Genetics
|March 29, 2025
PubMed
Summary

This review covers computational methods for analyzing DNA methylation using long-read sequencing. It explores tools for calling methylation, comparing samples, and understanding its role in gene regulation and disease.

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Last Updated: Jun 19, 2026

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Published on: October 21, 2011

Enhanced Reduced Representation Bisulfite Sequencing for Assessment of DNA Methylation at Base Pair Resolution
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Published on: February 24, 2015

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08:38

Targeted DNA Methylation Analysis by Next-generation Sequencing

Published on: February 24, 2015

Area of Science:

  • Epigenetics
  • Genomics
  • Computational Biology

Background:

  • DNA methylation is a key epigenetic mechanism influencing gene regulation, development, aging, and diseases like cancer.
  • Single-molecule long-read sequencing enables simultaneous measurement of DNA methylation and genomic variation.
  • Advancements in long-read data analysis are crucial for understanding methylation's role in chromatin structure and gene regulation.

Purpose of the Study:

  • To review computational methods for DNA methylation analysis using long-read sequencing.
  • To discuss tools for methylation calling, sample comparison, and cell-type diversity analysis.
  • To explore challenges and future directions in DNA methylation research tool development.

Main Methods:

  • Review of existing computational methods for DNA methylation analysis.
  • Focus on techniques applicable to single-molecule long-read sequencing data.
  • Discussion of algorithms for signal calling, differential analysis, and integration with genomic variation.

Main Results:

  • Identification and categorization of computational tools for DNA methylation analysis.
  • Comparison of methods based on their application to long-read sequencing data.
  • Highlighting the utility of these methods in understanding gene regulation and disease.

Conclusions:

  • Computational methods are essential for interpreting DNA methylation data from long-read sequencing.
  • Further development of advanced tools is needed to address current challenges.
  • Future research should focus on integrating methylation analysis with other genomic insights for a comprehensive understanding.