Automated mutation analysis
- 1 June 1999
- journal article
- review article
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 22 (4) , 503-518
- https://doi.org/10.1023/a:1005508324048
Abstract
Automated mutation analysis brings with it a vastly increased capacity in the number of test samples that can be processed at a time, as well as much improved test reproducibility. Until now, the introduction of automation into this field had been restricted to the use of semiautomated sequencing systems to make the most of the sequence information extractable from a single lane in an electrophoretic gel or in a polymer‐filled glass capillary. Much effort is now being directed into harnessing the potential of DNA microarrays (DNA chips) and there is increasing interest in the potential of matrix‐assisted mass spectrometry for determining the detail of large nucleic acid molecules. Meanwhile, there are other important recent developments already available, including robotic workstations, the further development of the allele‐specific oligonucleotide assay into microtitre formats, and its use with fluorescence for real‐time quantitative PCR analysis. Implementation of these developments in appropriate settings can further streamline the routine of molecular diagnostic laboratories, allowing them to take greater advantage of the recent surge of gene discoveries and their associated disease‐causing mutations.Keywords
This publication has 96 references indexed in Scilit:
- Identification of a common low density lipoprotein receptor mutation (C163Y) in the west of Scotland.Journal of Medical Genetics, 1998
- Rapid method for detection of point mutations using mismatch binding protein (MutS) and an optical biosensorGenetic Analysis: Biomolecular Engineering, 1997
- The Efficiency of Light-Directed Synthesis of DNA Arrays on Glass SubstratesJournal of the American Chemical Society, 1997
- Evaluation of MutS as a tool for direct measurement of point mutations in genomic DNAMutation Research - Fundamental and Molecular Mechanisms of Mutagenesis, 1997
- Rapid detection of trisomy 21 by homologous gene quantitative PCR (HGQ-PCR)Human Genetics, 1997
- Sequence from spectrometry: A realistic prospect?Nature Biotechnology, 1996
- A model for high-throughput automated DNA sequencing and analysis core facilitiesNature, 1994
- Endonuclease VII of Phage T4 Triggers Mismatch Correction in VitroJournal of Molecular Biology, 1993
- Selecting PCR designed mismatch primers to create diagnostic restriction sitesBioinformatics, 1992
- Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms.Proceedings of the National Academy of Sciences, 1989