Sequencing – classical method
Authors:
Monika Šedivcová 1; Petr Martínek 1; Jan Stehlík 1; Petr Grossmann 1; Jana Kašpírková 1,2; Tomáš Vaneček 1,2
Authors‘ workplace:
Bioptická laboratoř, s. r. o., Plzeň
1; Šiklův ústav patologie LF UK a FN, Plzeň
2
Published in:
Čes.-slov. Patol., 49, 2013, No. 3, p. 122-128
Category:
Reviews Article
Overview
In this article the basic methods of reading nucleotide sequences in DNA molecules are summarized. Sanger sequencing is described most thoroughly as it is the most frequent routine method currently being utilized. The article describes in detail the principle of sequence determination through the production of fragments with a known end base using chain termination synthesis of DNA and ways of separation and detection of the fragments. Some alternative methods of sequencing are mentioned in short. Basic approaches of analyzing sequence data are explained as well as different outcomes, obstacles and challenges.
Key words:
sequencing – Sanger – synthesis – ddNTP – fluorescence – capillary electrophoresis – mutation – electropherogram
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Labels
Anatomical pathology Forensic medical examiner ToxicologyArticle was published in
Czecho-Slovak Pathology
2013 Issue 3
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