Author

Paul D. Jewell

University of PennsylvaniaORCID 0000-0001-5560-8505Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Assay:bulk RNA-seq· 2 Approach:statistical model· 2 Research Focus:batch correction / integration· 1 Research Focus:benchmarking· 1 Organism:human· 1

Frequent Co-Authors

Yoseph BarashiD· 2 shared Andrei Thomas‐TikhonenkoiD· 1 shared Anupama JhaiD· 1 shared Barry SlaffiD· 1 shared Caleb M. RadensiD· 1 shared Elizabeth J. K. BhojiD· 1 shared Gregory R. GrantiD· 1 shared Jorge Vaquero-Garcia· 1 shared

Activity by Year

2020-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 27 mutual co-author links

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2 shared papersGenomics

Yoseph BarashORCID

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2 papers

Recent·Most cited

GenomicsNature CommunicationsPeer-reviewedJun 7, 2021

MOCCASIN: A method for correcting for known and unknown confounders in RNA splicing analysis

Barry Slaff, Caleb M. Radens, Paul D. Jewell…·Yoseph Barash

MOCCASIN corrects known and unknown confounders in RNA splicing analysis using synthetic and real data from TARGET and ENCODE.

23 citations

bulk RNA-seqstatistical model

𝕏 PostBluesky

GenomicsGenetics in MedicinePeer-reviewedMar 29, 2020

Mapping RNA splicing variations in clinically-accessible and non-accessible tissues to facilitate Mendelian disease diagnosis using RNA-seq

Joseph K. Aicher, Paul D. Jewell, Jorge Vaquero-Garcia…·Elizabeth J. K. Bhoj

The paper assesses how RNA-seq from clinically-accessible tissues represents splicing in non-accessible tissues and introduces a resource to explore these findings.

94 citationstop 4%

humanbulk RNA-seq

𝕏 PostBluesky