Author

Jonathan Wood

Wellcome Sanger InstitutePrimary ORCID profile (0000-0002-2925-6179 · 1 paper)Unclaimed ORCID profile · follow to get notified of new preprints

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Same name, identified by ORCID

Jonathan WoodiD1 paper · University of North Carolina at Chapel Hill

Biology Disciplines

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Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Kerstin HoweiD· 2 shared Adam M. PhillippyiD· 1 shared Chen-Shan ChiniD· 1 shared Chris Markovic· 1 shared Christine C. Lambert· 1 shared Deanna M Church· 1 shared Derek Albracht· 1 shared Devanand S. ManoliiD· 1 shared

Activity by Year

2017-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 31 mutual co-author links

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2 shared papersGenomics

Kerstin HoweORCID

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2 papers

Recent·Most cited

Single-library chromosome-scale diploid assemblies of vole genomes resolve a species-specific duplication implicated in pair bonding

Mohamed Abuelanin, Gulhan Kaya, Juniper A. Lake, Christine C. Lambert, Melody V. Wu, Kristen M. Berendzen, Jonathan Wood, Ksenia Krasheninnikova, Nancy G. Solomon, Zoe R. Donaldson, Karen Lisa Bales, Kerstin Howe, Jonas Korlach, Devanand S. Manoli, Jessica Tollkühn, Megan Y. Dennis

The paper assembles chromosome-scale diploid genomes of prairie and meadow voles using a single-library approach, identifying a prairie-vole-specific duplication of Avpr1a associated with pair bonding.

Cell Genomics · Aug 1, 2026Peer-reviewedGenomics

Evaluation of GRCh38 and de novo haploid genome assemblies demonstrates the enduring quality of the reference assembly

Valerie A Schneider, Tina Graves Lindsay, Kerstin Howe, Nathan Bouk, Hsiu-Chuan Chen, Paul A. Kitts, Terence D Murphy, Kim D. Pruitt, Françoise Thibaud-Nissen, Derek Albracht, Robert S Fulton, Milinn Kremitzki, Vince Magrini, Chris Markovic, Sean McGrath, , Deanna M Church

This paper evaluates GRCh38 and de novo haploid assemblies, finding that GRCh38 remains superior for complex genomic regions and coding sequences despite improvements in newer assemblies.

Genome Research · Apr 10, 2017Peer-reviewedGenomics