Author

Chase Miller

University of Utah

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Research Focus:variant calling· 2 Research Focus:variant effect prediction· 2 Assay:whole-exome sequencing· 2 Assay:whole-genome sequencing· 2 Research Focus:benchmarking· 1 Research Focus:database / resource· 1 Research Focus:gene regulatory network inference· 1

Frequent Co-Authors

Aditya Ekawade· 2 shared Alistair N. Ward· 2 shared Gábor MarthiD· 2 shared Matt VelinderiD· 2 shared Yi Qiao· 2 shared Anders PitmaniD· 1 shared Ashley AndrewsiD· 1 shared David H. ViskochiliD· 1 shared

Activity by Year

2019-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Aditya Ekawade

Mutual co-authors in cluster

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2 papers

Recent·Most cited

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

Tonya Di Sera, Matt Velinder, Alistair N. Ward, Yi Qiao, Stephanie J. Georges, Chase Miller, Anders Pitman, Will Richards, Aditya Ekawade, David H. Viskochil, John C. Carey, Laura Pace, Jim Bale, Stacey Lynn Clardy, Ashley Andrews, , 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.

Scientific Reports · Oct 13, 2021Peer-reviewedGenetic & Genomic Medicine

genepanel.iobio - an easy to use web tool for generating disease- and phenotype-associated gene lists

Aditya Ekawade, Matt Velinder, Alistair N. Ward, Tonya DiSera, Chase Miller, Yi Qiao, Gábor Marth

genepanel.iobio generates disease- and phenotype-associated gene lists by integrating multiple gene:disease resources, improving diagnostic variant prioritization in undiagnosed cases.

BMC Medical Genomics · Dec 1, 2019Peer-reviewedGenomics