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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...
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Proteins are involved in several cellular processes and biochemical reactions. Analyzing a specific protein of interest requires it to be isolated from the other proteins in the cell. This is achieved by overexpressing the specific gene in a suitable host to produce large quantities of the target protein. A tag or label is recombined with the gene to produce a fusion protein containing the target protein and the tag. The tags on these fusion proteins can then be used for easy detection and...
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Related Experiment Video

Updated: Jul 7, 2026

Metagenomic Analysis of Silage
08:43

Metagenomic Analysis of Silage

Published on: January 13, 2017

Extraction and annotation of SAGE tags using sequence quality values.

Jeppe Emmersen1

  • 1Department of Biochemistry, Chemistry and Environmental Engineering, University of Aalborg, Aalborg, Denmark.

Methods in Molecular Biology (Clifton, N.J.)
|February 22, 2008
PubMed
Summary

This study details a method for accurately identifying gene expression tags from sequencing data. By utilizing DNA base quality values, researchers can effectively control errors in unique tag discovery for gene analysis.

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Area of Science:

  • Molecular Biology
  • Bioinformatics
  • Genomics

Background:

  • Serial Analysis of Gene Expression (SAGE) is a technique used to analyze gene expression profiles by sequencing short tags.
  • Accurate identification of unique tags is crucial for reliable gene expression analysis.
  • Traditional SAGE analysis can be prone to false-positive discoveries of unique tags.

Purpose of the Study:

  • To describe a system for generating accurate tag lists from SAGE data.
  • To demonstrate the use of DNA base quality values for controlling false-positive tag discovery.

Main Methods:

  • Extraction of SAGE tags from single-pass sequence files of ditag concatemers.
  • Integration of DNA base quality values generated during base calling.
  • Development of a system for generating tag lists based on quality-associated sequence data.

Main Results:

  • A method for controlling the false-positive discovery rate of unique tags was established.
  • The system enables the generation of reliable tag lists from sequence data.

Conclusions:

  • Utilizing DNA base quality values enhances the accuracy of SAGE tag analysis.
  • The described system provides a robust approach for SAGE data processing, improving the reliability of gene expression studies.