Mississauga, Canada

Robert Shipman

This inventor holds 2 USPTO granted patents and 2 published patent applications. Top assignee: Visible Genetics Inc.. Active years: 2000-2002.

USPTO Granted Patents = 2 

% Patents Active = 100.0

Average Co-Inventor Count = 4.0

ph-index = 2

Forward Citations = 53(Granted Patents)


Company Filing History:


Years Active: 2000-2002

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2 patents (USPTO):Explore Patents

Title: The Innovations of Robert Shipman

Introduction

Robert Shipman is a notable inventor based in Mississauga, Canada. He has made significant contributions to the field of genetics through his innovative patents. With a total of 2 patents, Shipman has focused on methods that enhance the understanding and testing of genetic mutations.

Latest Patents

One of Shipman's latest patents is a method and reagents for testing for mutations in the BRCA1 gene. This method involves a hierarchical approach where samples are amplified in multiplex PCR reactions. The resulting fragments are evaluated against standard values to identify potential mutations. Another significant patent is a method for bi-directional sequencing of nucleic acid polymers. This method allows for the simultaneous determination of nucleotide base positions in both strands of a denatured duplex nucleic acid polymer, utilizing labeled oligonucleotide primers for improved sensitivity.

Career Highlights

Shipman is currently associated with Visible Genetics Inc., where he applies his expertise in genetic testing and sequencing technologies. His work has contributed to advancements in the field, particularly in the detection of genetic mutations that can lead to serious health conditions.

Collaborations

Some of his notable coworkers include James Leushner and James M Dunn. Their collaboration has likely fostered an environment of innovation and shared knowledge in the field of genetics.

Conclusion

Robert Shipman's contributions to genetic testing and sequencing have made a significant impact in the field. His innovative methods continue to advance our understanding of genetic mutations and their implications for health.

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