NDLI: Strategies for SNP genotyping by mass spectrometry

Content Provider	Semantic Scholar
Author	Hahner, Stephanie Kostrzewa, Markus Wenzel, Thomas Fröhlich, T.
Copyright Year	2003
Abstract	Abstract Single nucleotide polymorphisms (SNPs) represent the most frequently found sequence variations in the human genome. Thus, SNPs are thought to be useful markers for the identification of genetic factors associated with complex diseases, differential pharmacogenetic response as well as for the analysis of forensic samples. Here, we describe the use of matrix-assisted laser desorption/ionization time-of-flight (MALDI-TOF) mass spectrometry for the analysis of SNPs associated with a risk for common complex diseases. For highly efficient monitoring of a set of relevant SNP markers, the mass spectrometric analysis has been integrated into an overall process including the set-up of allele specific reactions, sample preparation and automated allele calling.
Starting Page	11
Ending Page	16
Page Count	6
File Format	PDF HTM / HTML
DOI	10.1016/S0531-5131(02)00286-8
Volume Number	1239
Alternate Webpage(s)	https://www.isfg.org/files/04ab68f72414cb3c6171bdb4a84e4c055c9eee46.02002868_537538053890.pdf
Alternate Webpage(s)	https://doi.org/10.1016/S0531-5131%2802%2900286-8
Language	English
Access Restriction	Open
Content Type	Text
Resource Type	Article

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