Author

Anders Pitman

University of UtahORCID 0009-0000-0925-5753Unclaimed 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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Research Focus:benchmarking· 2 Approach:experimental assay· 2 Research Focus:variant calling· 2 Assay:whole-genome sequencing· 2 Organism:human· 1 Research Focus:software / tool· 1 Approach:statistical model· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Aditya Ekawade· 1 shared Alistair N. Ward· 1 shared Ashley AndrewsiD· 1 shared C Yang· 1 shared Chase Miller· 1 shared David H. ViskochiliD· 1 shared Gábor MarthiD· 1 shared Jim Bale· 1 shared

Activity by Year

2021-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Aditya Ekawade

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2 papers

Recent·Most cited

BioinformaticsbioRxivPreprintJun 16, 2026

cuBayes: GPU accelerated FreeBayes that achieves 1-minute whole-genome SNV calling while maintaining algorithmic semantics

Anders Pitman, C Yang, 義行高橋

cuBayes accelerates whole-genome SNV calling using GPU acceleration, reducing analysis time from hours to minutes while maintaining high concordance with CPU results.

1 citation

humanwhole-genome sequencing

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Genetic & Genomic MedicineScientific ReportsPeer-reviewedOct 13, 2021

gene.iobio: an interactive web tool for versatile, clinically-driven variant interrogation and prioritization

Tonya Di Sera, Matt Velinder, Alistair N. Ward…·Gábor Marth

gene.iobio is a web tool that enables clinicians and researchers to interactively analyze and prioritize genomic variants for clinical diagnosis and patient care.

15 citations

whole-exome sequencingwhole-genome sequencing

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