Joseph A. Monforte
University of California, Santa Barbara
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Publication
Featured researches published by Joseph A. Monforte.
Tetrahedron Letters | 1985
Bruce H. Lipshutz; Daniel J. Pollart; Joseph A. Monforte; Hiyoshizo Kotsuki
PdCl2(CH3CN)2 catalyzes the hydrolysis of dioxolane acetals and ketals in moist CH3CN, while in acetoze, efficient and more reproducible exchange reactions take place.
Electrophoresis | 1999
Jia Li; John M. Butler; Yuping Tan; Hua Lin; Stephanie Royer; Lynne Ohler; Thomas A. Shaler; Joanna M. Hunter; Daniel J. Pollart; Joseph A. Monforte; Christopher H. Becker
The high frequency of single nucleotide polymorphisms (SNPs) in the human genome makes them a valuable source of genetic markers for identity testing, genome mapping, and medical diagnostics. Conventional technologies for detecting SNPs are laborious and time‐consuming, often prohibiting large‐scale analysis. A rapid, accurate, and cost‐effective method is needed to meet the demands of a high‐throughput DNA assay. We demonstrate here that analysis of these genetic markers can now be performed routinely in a rapid, automated, and high‐throughput fashion using time‐of‐flight mass spectrometry and a primer extension assay with a novel cleavable primer. SNP genotyping by mass spectrometry involves detection of single‐base extension products of a primer immediately adjacent to the SNP site. Measurement of the mass difference between the SNP primer and the extension peak reveals which nucleotide is present at the polymorphic site. The primer is designed such that its extension products can be purified and chemically released from the primer in an automated format. The reduction in size of the products as a result of this chemical cleavage allows more accurate identification of the polymorphic base, especially in samples from a heterozygotic population. All six possible heterozygotes are resolved unambiguously, including an A/T heterozygote with extension products differing by only 9 Da. Multiplex SNP determination is demonstrated by simultaneously probing multiple SNP sites from a single polymerase chain reaction (PCR) product as well as from multiplexed PCR amplicons. Samples are processed in parallel on a robotic workstation, and analyzed serially in an automated mass spectrometer with analysis times of only a few seconds per sample, making it possible to process thousands of samples per day.
Archive | 2001
Christine Loehrlein; Dan Pollart; Thomas A. Shaler; Kathy Stephens; Yuping Tan; Linda Wong; Joseph A. Monforte
Archive | 1997
Joseph A. Monforte; Christopher H. Becker; Daniel J. Pollart; Thomas A. Shaler
Archive | 1997
Joseph A. Monforte; Thomas A. Shaler; Yuping Tan; Christopher H. Becker
Archive | 1998
Joseph A. Monforte; Thomas A. Shaler; Yuping Tan; Christopher H. Becker
Archive | 1998
John M. Butler; Jia Li; Joseph A. Monforte; Christopher H. Becker
Archive | 2001
Christine Loehrlein; Dan Pollart; Thomas A. Shaler; Kathy Stephens; Yuping Tan; Joseph A. Monforte; Linda Wong
Archive | 1999
Jia Li; John M. Butler; Yuping Tan; Hua Lin; Stephanie Royer; Lynne Ohler; Thomas A. Shaler; Joanna M. Hunter; Daniel J. Pollart; Joseph A. Monforte; Christopher H. Becker
Archive | 1998
John M. Butler; Jia Li; Joseph A. Monforte; Christopher A. Becker