Fluorescence chemistries for automated primer‐directed DNA sequencing
Trevor Hawkins, Zijin Du, Nicolette D. Halloran, Richard K. Wilson
Abstract
Trevor Hawkins, Zijin Du, Nicolette D. Halloran, Richard K. Wilson
Abstract
A major limitation in the applicability of automated DNA sequencing instruments has been the difficulty in using user-defined oligonucleotide primers which allow sequencing reactions to start at any specific point in a region of interest. Recently, new chemistries have become available for fluorescent labeling which will begin to facilitate the use of any oligonucleotide primer with automated DNA sequencers. In this report, we describe several methods for automated primer-directed DNA sequencing, and compare and discuss the relative merits and limitations of these methods.
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A major limitation in the applicability of automated DNA sequencing instruments has been the difficulty in using user-defined oligonucleotide primers which allow sequencing reactions to start at any specific point in a region of interest. Recently, new chemistries have become available for fluorescent labeling which will begin to facilitate the use of any oligonucleotide primer with automated DNA sequencers. In this report, we describe several methods for automated primer-directed DNA sequencing, and compare and discuss the relative merits and limitations of these methods.
Key concepts: Primer (cosmetics), DNA sequencer, Oligonucleotide, DNA nanoball sequencing, DNA sequencing, Sequencing by ligation, Computational biology, Sequencing by hybridization