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Related Concept Videos

Sanger Sequencing01:57

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...
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.
Challenges of the Maxam-Gilbert Method
The...
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.
Next-Generation Sequencing Methods
Although all next-generation methods use different technologies, they all share a set of standard features.

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Pre-Implantation Genetic Testing for Aneuploidy on a Semiconductor Based Next-Generation Sequencing Platform
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Pre-Implantation Genetic Testing for Aneuploidy on a Semiconductor Based Next-Generation Sequencing Platform

Published on: August 17, 2022

Preparation of templates for DNA sequencing.

B E Slatko1, P Heinrich, B T Nixon

  • 1New England Biolabs, Beverly, Massachusetts, USA.

Current Protocols in Molecular Biology
|February 12, 2008
PubMed
Summary

This guide details DNA preparation protocols for dideoxy sequencing and chemical sequencing applications. It covers M13 phage, lambda phage, and plasmid DNA, optimizing templates for various DNA sequencing methods.

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Generation of High Quality Chromatin Immunoprecipitation DNA Template for High-throughput Sequencing (ChIP-seq)
09:52

Generation of High Quality Chromatin Immunoprecipitation DNA Template for High-throughput Sequencing (ChIP-seq)

Published on: April 19, 2013

Area of Science:

  • Molecular Biology
  • Genetics
  • Biochemistry

Background:

  • Accurate DNA sequencing relies on high-quality template preparation.
  • Different sequencing methodologies (dideoxy, chemical, thermal cycle) require specific DNA template characteristics.
  • Recombinant DNA molecules are the primary starting material for sequencing.

Purpose of the Study:

  • To provide standardized protocols for preparing DNA suitable for various sequencing techniques.
  • To detail methods for M13 phage, lambda phage, and plasmid DNA preparation.
  • To optimize DNA template quality for dideoxy sequencing, end labeling, and chemical sequencing.

Main Methods:

  • Preparation of M13mp-derived phage DNA for large-scale dideoxy sequencing.
  • Protocol for isolating lambda phage DNA from plate lysates.
  • Two distinct plasmid DNA miniprep protocols optimized for dideoxy sequencing or end labeling/chemical sequencing, differing in RNA removal.
  • Alkali denaturation of double-stranded DNA.
  • Preparation of template for thermal cycle sequencing from phage plaques or bacterial colonies.

Main Results:

  • Established reliable protocols for M13 phage DNA, a preferred source for large-scale dideoxy sequencing.
  • Provided a method for lambda phage DNA preparation from plate lysates.
  • Developed optimized plasmid DNA miniprep protocols catering to specific sequencing needs.
  • Described alkali denaturation for double-stranded DNA preparation.
  • Outlined a method for thermal cycle sequencing template preparation.

Conclusions:

  • The presented protocols offer versatile and reliable methods for preparing DNA templates for diverse sequencing applications.
  • Standardized DNA preparation enhances the efficiency and accuracy of dideoxy, chemical, and thermal cycle sequencing.
  • These protocols support both large-scale sequencing projects and specific applications like end labeling.