Author

Elizabeth J. Hamlin

University of Washington

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

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Assay:whole-genome sequencing· 2 Research Focus:benchmarking· 1 Research Focus:differential expression· 1 Assay:DNA methylation· 1 Assay:long-read sequencing· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Angela L MilleriD· 2 shared Danny E. MilleriD· 2 shared Joy GoffenaiD· 2 shared Koen L.I. van GasseniD· 2 shared Martin ElferinkiD· 2 shared Miranda Pg Zalusky· 2 shared Sophia B GibsoniD· 2 shared Trent M. PralliD· 2 shared

Activity by Year

2026-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Angela L MillerORCID

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2 papers

Recent·Most cited

EpiSignaLR: an open resource for genome-wide episignature analysis from methylation-aware short- and long-read sequencing

Sophia B Gibson, Miranda Pg Zalusky, Joy Goffena, Elizabeth J. Hamlin, Ruby Lamb, Jenna R. Rosinski, Trent M. Prall, Zachary B. Anderson, Sophie H. R. Storz, Angela L Miller, Yuwei Shi, Kristina Lanko, David Mulder, Yaoqing Shen, Kim Lensing, , Danny E. Miller

The paper develops EpiSignaLR, a resource for genome-wide episignature analysis using methylation-aware sequencing data, identifying DMRs and classifiers for three neurodevelopmental disorders.

medRxiv · Oct 23, 2026 · PreprintGenetic & Genomic Medicine

Accurate repeat expansion genotyping from whole-genome and real-time targeted nanopore sequencing with Mahi-mahi

Sophia B Gibson, Rebecca N Palmer, Sebastian Hollizeck, Wouter Koole, Heather M. Jeffery, Mirjan Albring, Jillian G. Buchan, R. Keira Cheetham, Martin Elferink, Joy Goffena, Elizabeth J. Hamlin, Rumo Jansen, Paul J. Lockhart, Dr. Rachel Martin, Angela L Miller, , Philipp Rescheneder

Mahi-mahi accurately genotypes repeat expansions from nanopore sequencing data, matching orthogonal methods and identifying pathogenic alleles.

medRxiv · Oct 20, 2026 · PreprintGenetic & Genomic Medicine