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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Genomics· 1

Signature Assays, Organisms & Methods

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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

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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

GenomicsbioRxivPreprintDec 18, 2019

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

Even Holth Rustad, Venkata D. Yellapantula, Dominik Głodzik…·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.

5 citations

humanwhole-genome sequencing

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