Author

Jeffrey Stevens

Seattle Children's Research Institute

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetic & Genomic Medicine· 2 Molecular Biology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:human· 2 Assay:long-read sequencing· 2 Research Focus:variant calling· 2 Research Focus:differential expression· 1 Approach:statistical model· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Adam J BisogniiD· 1 shared Ashley GrayiD· 1 shared Bonnie ColeiD· 1 shared Carla A. Jaeger-RuckstuhliD· 1 shared Craig Carl TeerlinkiD· 1 shared Danny E. MilleriD· 1 shared David Ming LiniD· 1 shared Elizabeth WardiD· 1 shared

Activity by Year

2020-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 14 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Adam J BisogniORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Ultra-fast sample-to-sequencing workflow for clinical diagnostics using micropillars

Adam J Bisogni, Irem Bastuzel, Mohamed Z. Rashed, Joy Goffena, Sophie H. R. Storz, Zachary B. Anderson, Min Seon Park, Trent M. Prall, Miranda Pg Zalusky, Erin E. Crotty, Bonnie Cole, Jeffrey Stevens, David Ming Lin, Harvey C. Tian, Danny E. Miller

This paper introduces an integrated microfluidic workflow for Oxford Nanopore sequencing that reduces hands-on time and sample loss while enabling high-quality library preparation from small sample volumes.

medRxiv · Jan 30, 2026 · PreprintGenetic & Genomic Medicine

Quantifying HLA transcripts by genotype in chimeric mixtures at single-cell resolution

Sami B. Kanaan, Jason G. Underwood, Rula Green Gladden, Everett Fan, Shruti S. Bhise, Monica S. Thakar, Carla A. Jaeger-Ruckstuhl, Jeffrey Stevens, Ashley Gray, Stanley R. Riddell, Marie Bleakley, Soheil Meshinchi, Scott N. Furlan

This paper introduces scrHLA-typing, a method to quantify HLA transcripts in single cells using long-read sequencing, showing its ability to detect allele-specific expression in post-transplant relapse samples.

bioRxiv · Sep 12, 2025 · PreprintMolecular Biology

Identification and genomic analysis of pedigrees with exceptional longevity identifies candidate rare variants

Justin B. Miller, Elizabeth Ward, Lyndsay A. Staley, Jeffrey Stevens, Craig Carl Teerlink, Justina P. Tavana, Matthew E. Cloward, Madeline L. Page, Louisa Dayton, Lisa Cannon‐Albright, John S. K. Kauwe

The paper identifies rare genetic variants associated with exceptional longevity through pedigree analysis and genomic screening in Utah populations.

Neurobiology of Disease · Jun 21, 2020Peer-reviewedGenetic & Genomic Medicine