This inventor holds 1 USPTO granted patent and 1 published patent application. Top assignee: Leland Stanford Junior University. Active years: 2019.
Company Filing History:
Years Active: 2019
Title: Laura Miotke: Innovator in Digital PCR Technology
Introduction
Laura Miotke is a prominent inventor based in Omaha, NE (US). She has made significant contributions to the field of genetic research through her innovative work in digital PCR technology. Her research focuses on the quantification of mutant alleles and copy number variations, which are crucial for understanding genetic disorders.
Latest Patents
Laura Miotke holds a patent titled "Quantification of mutant alleles and copy number variation using digital PCR with nonspecific DNA-binding dyes." This patent discloses methods and reagents for performing digital PCR to detect and quantify mutant alleles and copy number variations. The invention utilizes a nonspecific DNA-binding dye that produces a fluorescent signal, which increases in intensity based on the number of base pairs present in the PCR amplicon product. The method employs mutant-specific and wild-type-specific primers with non-complementary 'tail' sequences of varying lengths. This allows for the differentiation of amplicons for wild-type and mutant alleles based on the intensity of their fluorescent signals. The methods can detect rare genetic events, including single nucleotide mutations and alterations in copy number.
Career Highlights
Laura Miotke is affiliated with Leland Stanford Junior University, where she continues her research and development in genetic technologies. Her work has garnered attention for its potential applications in medical diagnostics and genetic research.
Collaborations
Laura has collaborated with notable colleagues, including Hanlee P Ji and Billy Tsz Cheong Lau, contributing to advancements in the field of genetics.
Conclusion
Laura Miotke's innovative work in digital PCR technology exemplifies the impact of her research on genetic diagnostics. Her contributions are paving the way for future advancements in understanding genetic variations and their implications.
