Author

Gage S. Black

University of UtahORCID 0000-0003-2086-5266Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Cancer Biology· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Assay:scRNA-seq· 2 Research Focus:cell type annotation· 1 Approach:deep learning· 1 Research Focus:differential expression· 1 Research Focus:drug response / drug discovery· 1 Approach:experimental assay· 1 Assay:long-read sequencing· 1

Frequent Co-Authors

Gábor MarthiD· 2 shared Philip J. MoosiD· 2 shared Xiaomeng HuangiD· 2 shared Aaron R. QuinlaniD· 1 shared Alli Ludwick· 1 shared Carol S. BruggersiD· 1 shared Casey R Sederman· 1 shared Deborah Marie StephensiD· 1 shared

Activity by Year

2025-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 35 mutual co-author links

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2 shared papersCancer Biology

Gábor MarthORCID

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2 papers

Recent·Most cited

Cancer BiologybioRxivPreprintOct 14, 2026

A multimodal precision oncology platform integrating genomics,single-cell transcriptomics, and functional drug screening expandstherapeutic options in pediatric brain tumors

Xiaomeng Huang, Yi Qiao, Gage S. Black…·Gábor Marth

DOI 10.64898/2026.10.12.758619

humanwhole-genome sequencing

𝕏 PostBluesky

GenomicsGenome ResearchPeer-reviewedApr 1, 2025

Long-read single-cell RNA sequencing enables the study of cancer subclone-specific genotype and phenotype in chronic lymphocytic leukemia

Gage S. Black, Xiaomeng Huang, Yi Qiao…·Gábor Marth

This study uses long-read scRNA-seq to analyze cancer subclone-specific mutations and transcriptomic differences in CLL patients with BTKC481S mutations.

5 citations

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