Author

Bryan Killinger

Asuragen (United States)ORCID 0000-0001-8544-648XUnclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Research Focus:variant calling· 2 Approach:experimental assay· 1 Assay:long-read sequencing· 1 Approach:statistical model· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Ahmad N. Abou TayouniD· 1 shared Brad Hall· 1 shared Bradley HalliD· 1 shared Brian C. Haynes· 1 shared Connor A. ParkeriD· 1 shared Devin W. CloseiD· 1 shared Elizabeth S. BarrieiD· 1 shared Eric K. FredricksoniD· 1 shared

Activity by Year

2024-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Ahmad N. Abou TayounORCID

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2 papers

Recent·Most cited

GeneticsbioRxivPreprintMay 19, 2026

Multisite Evaluation of an Amplification-based Nanopore Sequencing Solution to Analyze Challenging Clinically Relevant Variants in Genes Associated with Hereditary Diseases

Stela Filipovic-Sadic, Connor A. Parker, Mia K. Mihailovic…·Bradley Hall

This study evaluates a nanopore sequencing workflow for detecting complex variants in hereditary disease genes across multiple labs, finding high agreement with standard methods.

DOI 10.64898/2026.05.14.725224

humanwhole-genome sequencing

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Genetic & Genomic MedicinemedRxivPreprintFeb 22, 2024

A dual-mode targeted Nanopore sequencing assay for comprehensive SMN1 and SMN2 variant analysis

Brad Hall, Sawsan Alyafei, Sathishkumar Ramaswamy…·Ahmad N. Abou Tayoun

The paper develops a PCR/Nanopore sequencing assay for comprehensive SMN1 and SMN2 variant analysis with high accuracy and scalability.

1 citation

humanlong-read sequencing

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