Genome Res. 14:126-133, 2004
©2004 by Cold Spring Harbor Laboratory Press; ISSN 1088-9051/04 $5.00
Methods
High-Throughput MALDI-TOF Discovery of Genomic Sequence Polymorphisms
Patrick Stanssens1,3,
Marc Zabeau1,3,
Geert Meersseman1,
Gwen Remes1,
Yannick Gansemans1,
Niels Storm2,
Ralf Hartmer2,
Christiane Honisch2,
Charles P. Rodi2,
Sebastian Böcker2 and
Dirk van den Boom2,4
1 Methexis Genomics NV, B-9052 Zwijnaarde, Belgium
2 SEQUENOM, Inc., San Diego, California 92121, USA
We describe a comparative sequencing strategy that is based on matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) analyses of complete base-specific cleavage reactions of a target sequence. The target is converted to a DNA/RNA mosaic structure after PCR amplification using in vitro transcription. Cleavage with defined specificity is achieved by ribonucleases. The set of cleavage products is subjected to mass spectrometry without prior fractionation. The presented resequencing assay is particularly useful for single-nucleotide polymorphism (SNP) discovery. The combination of mass spectra from four complementary cleavage reactions detects approximately 98% of all possible homozygous and heterozygous SNPs in target sequences with a length of up to 500 bases. In general, both the identity and location of the sequence variation are determined. This was exemplified by the discovery of SNPs in the human gene coding for the cholesteryl ester transfer protein using a panel of 96 genomic DNAs.
Article and publication are at http://www.genome.org/cgi/doi/10.1101/gr.1692304.
3 These two authors contributed equally to this work.
4 Corresponding author. E-MAIL dvandenboom{at}sequenom.com; FAX (858) 202-9084.

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