Karl V Voelkerding

发表

Good laboratory practice for clinical next-generation sequencing informatics pipelines

Shashikant Kulkarni, Pavel Skums, David S. Campo, 2015, Nature Biotechnology.

Standards and Guidelines for Validating Next-Generation Sequencing Bioinformatics Pipelines: A Joint Recommendation of the Association for Molecular Pathology and the College of American Pathologists.

Alexis B. Carter, Somak Roy, Chen Wang, 2018, The Journal of molecular diagnostics : JMD.

Guidelines for Validation of Next-Generation Sequencing-Based Oncology Panels: A Joint Consensus Recommendation of the Association for Molecular Pathology and College of American Pathologists.

Marina N Nikiforova, John Pfeifer, Karl V Voelkerding, 2017, The Journal of molecular diagnostics : JMD.

Principles and Recommendations for Standardizing the Use of the Next-Generation Sequencing Variant File in Clinical Settings.

Karen Eilbeck, Justin M Zook, Gabor Marth, 2017, The Journal of molecular diagnostics : JMD.

Methods-based proficiency testing in molecular genetic pathology.

Carolyn Sue Richards, Karl V Voelkerding, Nazneen Aziz, 2014, The Journal of molecular diagnostics : JMD.

Next-generation sequencing of custom amplicons to improve coverage of HaloPlex multigene panels.

Karl V Voelkerding, Emily M. Coonrod, Emily M Coonrod, 2014, BioTechniques.

Next generation sequencing for clinical diagnostics-principles and application to targeted resequencing for hypertrophic cardiomyopathy: a paper from the 2009 William Beaumont Hospital Symposium on Molecular Pathology.

Shale Dames, Karl V Voelkerding, Jacob D Durtschi, 2010, The Journal of molecular diagnostics : JMD.

Translating exome sequencing from research to clinical diagnostics

Karl V Voelkerding, Emily M Coonrod, Rebecca L Margraf, 2011, Clinical chemistry and laboratory medicine.

Developing genome and exome sequencing for candidate gene identification in inherited disorders: an integrated technical and bioinformatics approach.

Karl V Voelkerding, Emily M Coonrod, Jacob D Durtschi, 2013, Archives of pathology & laboratory medicine.

Development and Validation of Targeted Next-Generation Sequencing Panels for Detection of Germline Variants in Inherited Diseases.

Birgit Funke, Avni Santani, Rong Mao, 2017, Archives of pathology & laboratory medicine.

Variant identification in multi-sample pools by illumina genome analyzer sequencing.

Shale Dames, Karl V Voelkerding, Jacob D Durtschi, 2011, Journal of biomolecular techniques : JBT.

Clinical analysis of genome next-generation sequencing data using the Omicia platform

Martin G Reese, Archie Russell, Karl V Voelkerding, 2013, Expert review of molecular diagnostics.

A unified test of linkage analysis and rare-variant association for analysis of pedigree sequence data

Gustavo Glusman, Paul Scheet, Mark Yandell, 2014, Nature Biotechnology.

Comparison of the Illumina Genome Analyzer and Roche 454 GS FLX for resequencing of hypertrophic cardiomyopathy-associated genes.

Katherine Geiersbach, Shale Dames, Karl V Voelkerding, 2010, Journal of biomolecular techniques : JBT.

Extraction and amplification of genomic DNA from human blood on nanoporous aluminum oxide membranes.

Karl V Voelkerding, Jacob D Durtschi, K. Voelkerding, 2004, Clinical chemistry.

High resolution melting applications for clinical laboratory medicine.

Karl V Voelkerding, Carl T Wittwer, K. Voelkerding, 2008, Experimental and molecular pathology.

Opportunities and challenges associated with clinical diagnostic genome sequencing: a report of the Association for Molecular Pathology.

Tina Hambuch, Lisa Kalman, Rong Mao, 2012, The Journal of molecular diagnostics : JMD.

A Model Study of In Silico Proficiency Testing for Clinical Next-Generation Sequencing.

John D Pfeifer, Karl V Voelkerding, Eric J Duncavage, 2016, Archives of pathology & laboratory medicine.