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Dive into the research topics where Joseph A. Monforte is active.

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Featured researches published by Joseph A. Monforte.


Tetrahedron Letters | 1985

Pd(II)-catalyzed acetal/ketal hydrolysis/exchange reactions

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

SINGLE NUCLEOTIDE POLYMORPHISM DETERMINATION USING PRIMER EXTENSION AND TIME-OF-FLIGHT MASS SPECTROMETRY

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

Methods for analysis of gene expression

Christine Loehrlein; Dan Pollart; Thomas A. Shaler; Kathy Stephens; Yuping Tan; Linda Wong; Joseph A. Monforte


Archive | 1997

Releasable nonvolatile mass label molecules

Joseph A. Monforte; Christopher H. Becker; Daniel J. Pollart; Thomas A. Shaler


Archive | 1997

Methods of screening nucleic acids using mass spectrometry

Joseph A. Monforte; Thomas A. Shaler; Yuping Tan; Christopher H. Becker


Archive | 1998

Methods of preparing nucleic acids for mass spectrometric analysis

Joseph A. Monforte; Thomas A. Shaler; Yuping Tan; Christopher H. Becker


Archive | 1998

Dna typing by mass spectrometry with polymorphic dna repeat markers

John M. Butler; Jia Li; Joseph A. Monforte; Christopher H. Becker


Archive | 2001

Procedes d'analyse de l'expression genique

Christine Loehrlein; Dan Pollart; Thomas A. Shaler; Kathy Stephens; Yuping Tan; Joseph A. Monforte; Linda Wong


Archive | 1999

Single nucleotide polymorphism determination using primer extension and time-of-flight mass

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

Recherche de type de genes par spectrometrie de masse avec marqueurs de sequences repetees d'adn polymorphes

John M. Butler; Jia Li; Joseph A. Monforte; Christopher A. Becker

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John M. Butler

National Institute of Standards and Technology

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