Asuragen Scientific Publications

Asuragen has researched and published extensively in genetics, oncology, molecular diagnostics, and technology advancements for over 15 years. These publications, posters, and white papers cover various disease areas and their related genes including fragile X (FMR1), spinal muscular atrophy (SMN1/SMN2), cystic fibrosis (CFTR), and chronic myeloid leukemia (BCR-ABL1). They show the power of detecting and interpreting molecular alterations using AmplideX and QuantideX technologies as well as the value of Molecular Quality Controls and companion diagnostics collaborations to deliver new insights and advance precision medicine. Simply search by term, filter by category, or use both to find your area of interest.

We’re driven to provide people with better answers, so we ensure our products are supported by reliable data and backed by rigorous science. Dive into these publications to learn more.

Verification of Software and Amplification-Based Nanopore Sequencing Solution to Characterize Complex Variants in 11 Challenging, High-Frequency Carrier Genes
Juliette Baker
Beta evaluation of AmplideX® PCR enrichement technology with Nanopore long-read DNA sequencing of a panel of eleven challenging genes
Lebre A.S.
Verification of an Amplification Based Nanopore Sequencing Assay and Software to Genotype Complex, Clinically-Relevant Variants in 11 Hard-to-Decipher Genes with High Carrier Frequencies
Connor A. Parker, Jonathan Turner, Brennan Greenlee, Juliette A. Baker, Walairat L. Wolf, Christopher J. Fraher, Monica Roberts, Theodore Markulin, Eduardo Priego, Mahesh Yarasi, Mia K. Mihailovic, Bryan J. Killinger, Brian C. Haynes, Bradley Hall, and Ashima Sharma
Resolving Complex Genotypes in Residual Clinical Samples with Long Range-PCR and Nanopore Sequencing Assay
Cody Edwards, Bryan Killinger, Andrew Laurie, Lisa Hsu, Anne-Sophie Lebre, Tony Yammine, Chandler Ho, Tsoyu Chiang, Ilona Volkova, Monica Roberts, Theodore Markulin, Mia Mihailovic, Eduardo Priego, Brian C. Haynes, Bradley Hall
Combining AmplideX® PCR Chemistries, Nanopore Sequencing, and Automated Analysis Software to Genotype Complex, Clinically-relevant Variants in 11 Challenging Targets Associated with Hereditary Diseases
John N. Milligan, Bryan J. Killinger, Cody Edwards, Christopher J. Fraher, Jon Kemppainen, Monica Roberts, Jonathan Turner, Theodore Markulin, Brennan Greenlee, Eduardo Priego, Juliette A. Baker, Mahesh Yarasi, Connor Parker, Mia K. Mihailovic, Ashima Sharma, Brian C. Haynes, and Bradley Hall
Beta evaluation of AmplideX® PCR enrichement technology with Nanopore long-read DNA sequencing of a panel of eleven challenging genes
Feyereisen L, Yammine T, Landais E, Moret H, Audrézet M-P, Bonello-Palot N, Rouzier C, Pissard S, Gueguen P, Metay C, Froissart R, Bekri S, Bellanné-Chantelot C, Lebre AS
Accessible AmplideX® PCR and Nanopore Sequencing For Rare Variant Characterization in 11 Challenging Genes Associated with Hereditary Diseases
Bradley Hall, Anne-Sophie Lebre, Tony Yammine, Cody Edwards, Theodore Markulin, Bryan Killinger, Jacob Ashton, Christopher J. Fraher, and Brian C. Haynes
Amplification-Based Nanopore Sequencing Accurately Detects HBA and HBB SNVs, Indels, and Structural Variants in Clinical Thalassemia Samples
Jaime Lopes, Marcus Cannon, Jonathan Turner, Monica Roberts, Theodore Markulin, Chris Fraher, Bryan Killinger, Stela Filipovic-Sadic, Bradley Hall
A PCR/Nanopore Assay for Accurate Variant Detection in Hard-to-Decipher Carrier Screening Genes with Automated Analysis Software
Bryan J. Killinger, Monica P. Roberts, Theodore J. Markulin, Mia K. Mihailovic, Eduardo Priego, Connor A. Parker, Jonathan Turner, Mahesh Yarasi, Cody W. Edwards, Christopher J. Fraher, Jon N. Kemppainen, Brennan T. Greenlee, Juliette A. Baker, Jacob D. Ashton, Brian C. Haynes, and Bradley Hall
Impact of Variants of Varying Clinical Consequence in Underrepresented Populations and Implications for a Minimum Variant Set for Pan-Ancestry Cystic Fibrosis Carrier Screening
Gary J. Latham, Brian C. Haynes, Brad Hall, and John N. Milligan
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