An automated microfluidic DNA microarray platform for genetic variant detection in inherited arrhythmic diseases-Reference-Cited by-同舟云学术

An automated microfluidic DNA microarray platform for genetic variant detection in inherited arrhythmic diseases

Published:2018 Issue:6 Volume:143 Page:1367-1377
ISSN:0003-2654
Container-title:The Analyst
language:en
Short-container-title:Analyst

Author:

Huang Shu-Hong¹²³⁴,Chang Yu-Shin¹²³⁴,Juang Jyh-Ming Jimmy⁵⁶⁷⁸³,Chang Kai-Wei¹²³⁴,Tsai Mong-Hsun⁹²³⁴,Lu Tzu-Pin¹⁰¹¹²⁴,Lai Liang-Chuan¹²⁸³⁴,Chuang Eric Y.¹²³⁴¹³,Huang Nien-Tsu¹²³⁴¹³^ORCID

Affiliation:

1. Graduate Institute of Biomedical Electronics and Bioinformatics

2. National Taiwan University

3. Taipei

4. Taiwan

5. Cardiovascular Center and Division of Cardiology

6. Department of Internal Medicine

7. National Taiwan University Hospital

8. National Taiwan University College of Medicine

9. Institute of Biotechnology

10. Institute of Epidemiology and Preventive Medicine

11. Department of Public Health

12. Graduate Institute of Physiology

13. Department of Electrical Engineering

Abstract

In this study, we developed an automated microfluidic DNA microarray (AMDM) platform for genetic variant detection in inherited arrhythmic diseases.

Funder

National Taiwan University

Ministry of Science and Technology, Taiwan

Publisher

Royal Society of Chemistry (RSC)

Subject

Electrochemistry,Spectroscopy,Environmental Chemistry,Biochemistry,Analytical Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2018/AN/C7AN01648D

Reference53 articles.

1. Genetic Testing for Potentially Lethal, Highly Treatable Inherited Cardiomyopathies/Channelopathies in Clinical Practice

2. Utilizing Multiple in Silico Analyses to Identify Putative Causal SCN5A Variants in Brugada Syndrome

3. Genetics of Brugada syndrome

4. DNA Microarray Technology: Devices, Systems, and Applications

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