Author

Cody Ashby

University of Arkansas for Medical SciencesORCID 0000-0002-9361-0283Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:cell-cell communication· 1 Assay:ChIP-seq· 1 Research Focus:differential expression· 1 Assay:DNA methylation· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1

Frequent Co-Authors

Gareth John MorganiD· 2 shared Agata CieślakiD· 1 shared Ahmet DoǧaniD· 1 shared Aneta MikulášováiD· 1 shared Anne E. CorcoraniD· 1 shared Benjamin T. DiamondiD· 1 shared Brian A. WalkeriD· 1 shared Carolina SchinkeiD· 1 shared

Activity by Year

2019-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 27 mutual co-author links

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2 shared papersGenomics

Gareth John MorganORCID

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2 papers

Recent·Most cited

Epigenomic translocation of H3K4me3 broad domains over oncogenes following hijacking of super-enhancers

Aneta Mikulášová, Daniel Kent, Marco Trevisán-Herraz, Nefeli Karataraki, Kent T.M. Fung, Cody Ashby, Agata Cieślak, Shmuel Yaccoby, Frits van Rhee, Maurizio Zangari, Sharmilan Thanendrarajan, Carolina Schinke, Gareth John Morgan, Vahid Asnafi, Salvatore Spicuglia, , Lisa Jane Russell

The paper identifies H3K4me3 broad domains formed by super-enhancer translocations in B-cell and T-cell malignancies, linking them to oncogene activation.

Genome Research · Jul 1, 2022Peer-reviewedGenomics

Revealing the impact of recurrent and rare structural variants in multiple myeloma

Even Holth Rustad, Venkata D. Yellapantula, Dominik Głodzik, Kylee H. Maclachlan, Benjamin T. Diamond, Eileen Mary Boyle, Cody Ashby, Patrick Blaney, Gunes Gundem, Malin L. Hultcrantz, Daniel A. Leongamornlert, Nicos Angelopoulos, Daniel Auclair, Yanming Zhang, Ahmet Doǧan, , Francesco Maura

This study identifies 100 SV hotspots and 31 new candidate driver genes in multiple myeloma, revealing that 63% of SVs remain unexplained and are associated with outlier gene expression.

bioRxiv · Dec 18, 2019 · PreprintGenomics