Author

Briana Wilson

University of VirginiaORCID 0000-0002-4967-6998Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Bioinformatics· 1 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Research Focus:gene regulatory network inference· 1 Approach:machine learning (classical)· 1 Organism:mouse· 1 Approach:statistical model· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Pankaj KumariD· 2 shared Shekhar SahaiD· 2 shared Teressa PaulseniD· 2 shared Zhangli SuiD· 2 shared Aakrosh RataniD· 1 shared Ajay ChatrathiD· 1 shared Anindya DuttaiD· 1 shared Ewelina Sobierajska· 1 shared

Activity by Year

2020-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 40 mutual co-author links

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2 shared papersBioinformatics

Pankaj KumarORCID

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2 papers

Recent·Most cited

BioinformaticsNAR Genomics and BioinformaticsPeer-reviewedMar 31, 2022

tRForest: a novel random forest-based algorithm for tRNA-derived fragment target prediction

R. Parikh, Briana Wilson, Laine Marrah…·Anindya Dutta

tRForest improves tRNA fragment target prediction using random forest, validated in cell lines and showing enrichment in neuronal function.

11 citations

𝕏 PostBluesky

Genetic & Genomic MedicineGenome MedicinePeer-reviewedFeb 17, 2020

The Pan-Cancer Landscape of Prognostic Germline Variants in 10,582 Patients

Ajay Chatrath, Róża K. Przanowska, Shashi Kiran…·Anindya Dutta

The paper identifies prognostic germline variants in 10,582 cancer patients using multivariate Cox regression, showing their association with patient outcomes beyond clinical data.

45 citations

humanwhole-exome sequencing

𝕏 PostBluesky