Company Filing History:
Years Active: 2015
Title: **En-Chung Lin: Innovator in SNP Detection Technologies**
Introduction
En-Chung Lin is a prominent inventor based in Taipei, Taiwan, recognized for his innovative contributions to the field of genetic research. With a focus on improving detection techniques, Lin has developed a solution that enhances the accuracy of single nucleotide polymorphism (SNP) detection, a critical aspect of genetic analysis.
Latest Patents
Lin holds a patent for a groundbreaking method of SNP detection utilizing gene detection techniques in bead-based microfluidics. This patent outlines a systematic approach comprising several key steps: preparing a microbead embedded with duplex DNA, integrating a dye into the duplex DNA, and delivering the microbead into a temperature-gradient microchannel. The method includes heating the temperature gradient region to denature the duplex DNA and monitoring the fluorescence intensity to obtain a melting curve. This innovative technique also involves analyzing the melting curve to determine the SNP, enhancing measurement accuracy through the validated continuous-flow mechanism within the temperature gradient.
Career Highlights
En-Chung Lin is affiliated with National Taiwan University, where he conducts research that bridges the gap between biotechnology and practical applications in genetic detection. His work is instrumental in advancing methodologies that contribute to better disease diagnosis and personalized medicine.
Collaborations
Lin collaborates closely with fellow researchers Kan-Chien Li and Shih-Torng Ding. Their combined expertise fosters an environment of innovation, leading to significant advancements in genetic research and detection techniques.
Conclusion
En-Chung Lin's innovative work is a testament to the potential of technology in transforming genetic research. His patent on SNP detection using bead-based microfluidics not only showcases his inventive spirit but also contributes significantly to the scientific community, paving the way for future developments in genetic diagnostics.