Author

Zachary L. Payne

Washington University in St. LouisORCID 0000-0001-6328-2533Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:variant effect prediction· 2 Research Focus:benchmarking· 1 Research Focus:database / resource· 1 Research Focus:differential expression· 1 Assay:proteomics· 1 Research Focus:software / tool· 1

Frequent Co-Authors

Jeffrey K. NgiD· 2 shared Tychele N. TurneriD· 2 shared Chandler Prince· 1 shared Craig S. PohliD· 1 shared Eleanor I. SamsiD· 1 shared Elvisa MehinoviciD· 1 shared Elyn Fritz‐WatersiD· 1 shared Evin M. PadhiiD· 1 shared

Activity by Year

2021-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Jeffrey K. NgORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintFeb 2, 2024

Proteome-Wide Assessment of Clustering of Missense Variants in Neurodevelopmental Disorders Versus Cancer

Jeffrey K. Ng, Yilin Chen, Titilope M. Akinwe…·Tychele N. Turner

The paper assesses clustering of missense variants in neurodevelopmental disorders and cancer, identifying proteins with significant variation patterns in each condition.

4 citations

humanproteomics

𝕏 PostBluesky

GenomicsbioRxivPreprintMay 27, 2021

de novo variant calling identifies cancer mutation profiles in the 1000 Genomes Project

Jeffrey K. Ng, Pankaj Vats, Elyn Fritz‐Waters…·Tychele N. Turner

The paper identifies de novo variants in the 1000 Genomes Project using a GPU-based workflow, revealing cell line artifacts and cancer-related mutation profiles.

8 citations

humanwhole-genome sequencing

𝕏 PostBluesky