Author

Venkata D. Yellapantula

Memorial Sloan Kettering Cancer CenterORCID 0000-0001-9848-3263Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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

Frequent Co-Authors

Ahmet DoǧaniD· 1 shared Benjamin T. DiamondiD· 1 shared Cody AshbyiD· 1 shared Daniel A. LeongamornlertiD· 1 shared Daniel AuclairiD· 1 shared Dominik GłodzikiD· 1 shared Eileen Mary BoyleiD· 1 shared Elli PapaemmanuiliD· 1 shared

Activity by Year

2019-2019 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenomics

Ahmet DoǧanORCID

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1 paper

Recent·Most cited

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