- Home
- Publications
- Publication Search
- Publication Details
Title
Next Generation Diagnostics in Inherited Arrhythmia Syndromes
Authors
Keywords
Inherited cardiac conditions, Next-generation sequencing, Molecular diagnosis, Genetics, Ion channels, Long QT syndrome
Journal
Journal of Cardiovascular Translational Research
Volume 6, Issue 1, Pages 94-103
Publisher
Springer Nature
Online
2012-09-07
DOI
10.1007/s12265-012-9401-8
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Targeted resequencing of the EGFR and MET genes using the Fluidigm Access Array System and the Roche GS Junior System
- (2012) Clotilde Teiling et al. BIOTECHNIQUES
- Exome sequencing-based copy-number variation and loss of heterozygosity detection: ExomeCNV
- (2011) Jarupon Fah Sathirapongsasuti et al. BIOINFORMATICS
- Targeted Next-Generation Sequencing for the Molecular Genetic Diagnostics of Cardiomyopathies
- (2011) Benjamin Meder et al. Circulation-Cardiovascular Genetics
- HRS/EHRA Expert Consensus Statement on the State of Genetic Testing for the Channelopathies and Cardiomyopathies: This document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA)
- (2011) M. J. Ackerman et al. EUROPACE
- Performance comparison of exome DNA sequencing technologies
- (2011) Michael J Clark et al. NATURE BIOTECHNOLOGY
- A framework for variation discovery and genotyping using next-generation DNA sequencing data
- (2011) Mark A DePristo et al. NATURE GENETICS
- Mutation-Specific Risk in Two Genetic Forms of Type 3 Long QT Syndrome
- (2010) Judy F. Liu et al. AMERICAN JOURNAL OF CARDIOLOGY
- Fast and accurate long-read alignment with Burrows–Wheeler transform
- (2010) Heng Li et al. BIOINFORMATICS
- BEDTools: a flexible suite of utilities for comparing genomic features
- (2010) Aaron R. Quinlan et al. BIOINFORMATICS
- A database and API for variation, dense genotyping and resequencing data
- (2010) Daniel Rios et al. BMC BIOINFORMATICS
- The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data
- (2010) A. McKenna et al. GENOME RESEARCH
- A map of human genome variation from population-scale sequencing
- (2010) Richard M. Durbin et al. NATURE
- Accurate SNP and mutation detection by targeted custom microarray-based genomic enrichment of short-fragment sequencing libraries
- (2010) Michal Mokry et al. NUCLEIC ACIDS RESEARCH
- Ensembl 2011
- (2010) P. Flicek et al. NUCLEIC ACIDS RESEARCH
- The Sequence Alignment/Map format and SAMtools
- (2009) H. Li et al. BIOINFORMATICS
- Fast and accurate short read alignment with Burrows-Wheeler transform
- (2009) H. Li et al. BIOINFORMATICS
- High Efficacy of β-Blockers in Long-QT Syndrome Type 1
- (2009) G. Michael Vincent et al. CIRCULATION
- The genetic basis of long QT and short QT syndromes: A mutation update
- (2009) Paula L. Hedley et al. HUMAN MUTATION
- The RYR2-Encoded Ryanodine Receptor/Calcium Release Channel in Patients Diagnosed Previously With Either Catecholaminergic Polymorphic Ventricular Tachycardia or Genotype Negative, Exercise-Induced Long QT Syndrome
- (2009) Argelia Medeiros-Domingo et al. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
- Solution hybrid selection with ultra-long oligonucleotides for massively parallel targeted sequencing
- (2009) Andreas Gnirke et al. NATURE BIOTECHNOLOGY
- Sequencing technologies — the next generation
- (2009) Michael L. Metzker NATURE REVIEWS GENETICS
- Enrichment of sequencing targets from the human genome by solution hybridization
- (2009) Ryan Tewhey et al. GENOME BIOLOGY
- All LQT3 patients need an ICD: True or false?
- (2008) Peter J. Schwartz et al. HEART RHYTHM
Discover Peeref hubs
Discuss science. Find collaborators. Network.
Join a conversationBecome a Peeref-certified reviewer
The Peeref Institute provides free reviewer training that teaches the core competencies of the academic peer review process.
Get Started