Typing of single nucleotide polymorphisms by MALDI mass spectrometry: principles and diagnostic applications

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Item Type:	Review
Title:	Typing of single nucleotide polymorphisms by MALDI mass spectrometry: principles and diagnostic applications
Creators Name:	Sauer, S.
Abstract:	Background: After the completion of the human genome sequencing project human genetics has now shifted its focus to DNA variation. DNA variation analysis is considered to be a key in partly understanding the mechanisms of complex diseases or varying patient responses in drug treatment. One of the major goals in genetics is finding the DNA variants that can act as diagnostic markers for predisposition to specific diseases. Moreover, in microbiology DNA variation has long been known to help discriminate and identify bacterial strains and viruses. Diagnostics based on DNA or RNA detection might be advantageous as an early-stage indication can be provided. Methods: Many simple and efficient methods for the analysis of nucleic acids are already available. Consequently, the last few years have seen an increased in the use of large-scale analysis of nucleic acids, in basic DNA variation studies along with diagnostics. Mass spectrometry techniques such as matrix-assisted laser desorption/ionization (MALDI) and electrospray ionization (ESI) can be of great use for genome variation analysis. In particular high-throughput SNP analysis by MALDI can be performed using fully integrated platforms. Conclusions: Mass spectrometry-based procedures have promise for SNPs analysis especially for clinical diagnostics.
Keywords:	SNP, Genotyping, DNA, Clinical Diagnostics
Source:	Clinica Chimica Acta
ISSN:	0009-8981
Publisher:	Elsevier
Volume:	363
Number:	1-2
Page Range:	95-105
Date:	January 2006
Official Publication:	https://doi.org/10.1016/j.cccn.2005.05.040
PubMed:	View item in PubMed

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