Author

Emily K. Tsang

Stanford MedicineORCID 0000-0001-7287-6448Unclaimed ORCID profile · follow to get notified of new preprints

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Emily K. Tsang1 paper

Biology Disciplines

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Assay:bulk RNA-seq· 2 Research Focus:differential expression· 2 Organism:human· 2 Research Focus:variant effect prediction· 2 Approach:Bayesian inference· 1 Research Focus:benchmarking· 1 Approach:statistical model· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Alexandra J. ScottiD· 2 shared Alexis J. BattleiD· 2 shared Benjamin J. StroberiD· 2 shared Ira M. HalliD· 2 shared Joe R. DavisiD· 2 shared Stephen B. MontgomeryiD· 2 shared Xin LiiD· 2 shared Aaron GraubertiD· 1 shared

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2017-2020 · peak 1/yr

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10 top collaborators · 45 mutual co-author links

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2 shared papersGenomics

Alexandra J. ScottORCID

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2 papers

Recent·Most cited

GenomicsSciencePeer-reviewedSep 10, 2020

Diverse transcriptomic signatures across human tissues identify functional rare genetic variation

Nicole M. Ferraro, Benjamin J. Strober, Jonah E. Einson…·Andrew B. Nobel

Integrating expression, allelic expression and splicing across tissues identifies rare variants with relevance to traits.

171 citationstop 1%

humanbulk RNA-seq

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GenomicsNaturePeer-reviewedOct 12, 2017

The impact of rare variation on gene expression across tissues

Xin Li, Yungil Kim, Emily K. Tsang…·Stephen B. Montgomery

The paper identifies rare variants contributing to extreme gene expression changes across tissues and introduces RIVER, a Bayesian method to prioritize functional variants.

DOI 10.1038/nature24267

humanwhole-genome sequencing

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