Author

Tristan S. Shaffer

University of WashingtonORCID 0000-0002-6756-6063Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Approach:benchmark study· 2 Research Focus:benchmarking· 2 Organism:human· 2 Research Focus:variant calling· 2 Assay:whole-genome sequencing· 2 Approach:statistical model· 1

Frequent Co-Authors

Caitlin N. JacquesiD· 2 shared Christina ZakarianiD· 2 shared Sean R. McGeeiD· 2 shared Adriana Estela Sedeño-CortésiD· 1 shared ALEXANDER V. ROBERTSON· 1 shared Amy S. LeonardsoniD· 1 shared Andrew B. StergachisiD· 1 shared Andrew W. CarrolliD· 1 shared

Activity by Year

2026-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Caitlin N. JacquesORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintJul 10, 2026

Benchmarking long-read variant sensitivity across ONT and PacBio platforms using known clinically reported variants in a cohort of critically ill newborns

Colby T. Marvin, Joseph M. Devaney, Kati J. Buckingham…·Jessica X. Chong

DOI 10.64898/2026.07.07.26357482

humanwhole-genome sequencing

𝕏 PostBluesky

GenomicsbioRxivPreprintFeb 20, 2026

Donor-specific assemblies enhance somatic structural variant detection in complex genomic regions

Taralynn Mack, Jiadong Lin, Luyao Ren…·Evan E. Eichler

This study benchmarks donor-specific assemblies for improved detection of somatic structural variants in a melanoma cell line, finding they identify more variants, especially in repeat-rich regions.

2 citations

humanwhole-genome sequencing

𝕏 PostBluesky