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.

With Exosome Analysis, Highly Sensitive Monitoring of ESR1 Mutations Is Possible
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
Comparaison du kit QuantideX® qPCR BCR ABL IS avec une technique “maison” pour la quantification des transcrits majeurs BCR::ABL1
Emilie KLEIN, Claudine CHOLLET, Remi DEVOS, Lisa BOUREAU, Stéphanie DULUCQ
A Kit Targeting Detection of ESR1 Mutations From Circulating Exosomal RNA and Cell-Free DNA Supports Longitudinal Studies Into Endocrine Therapy Resistance in a Broadly Accessible RT-qPCR Format
Sarah Statt, Julie R Thibert, Konrad Mueller, Melissa Church, Jamie Myers, Holli Dale, Liangjing Chen, Elliot Hallmark, Megan Yociss, Kevin Kelnar, Kurt Franzen, Johan Skog, and Brian 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
Performance and Compatibility of the Promega Spectrum Compact CE System for Performing AmplideX® Gene Variant Analysis
Prototype RT-qPCR PML::RARA Reagents and a Commercial PML-RARA Kit Yield Highly Correlated Results
Walairat Laosinchai Wolf, Adrian Lara, and Justin T Brown
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