Author

Rikuto Goto

Hiroshima University

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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Bioinformatics· 1 Cell Biology· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Assay:bulk RNA-seq· 2 Research Focus:cell type annotation· 2 Research Focus:differential expression· 2 Research Focus:gene regulatory network inference· 2 Organism:mouse· 2 Approach:statistical model· 2 Research Focus:cell-cell communication· 1 Approach:experimental assay· 1

Frequent Co-Authors

Akinori AwazuiD· 3 shared Naoaki SakamotoiD· 3 shared Akiko Kubota· 2 shared Ganma Tanaka· 2 shared Reo Hayashi· 1 shared Shizune Nakamura· 1 shared Takeshi IgawaiD· 1 shared Tetsushi KomotoiD· 1 shared

Activity by Year

2026-2026 · peak 3/yr

Co-Author Collaboration Network

8 top collaborators · 25 mutual co-author links

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3 shared papersCell Biology

Akinori AwazuORCID

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3 papers

Recent·Most cited

Transcriptomic response to histone deacetylase inhibitors in cultured feline cells

Ganma Tanaka, Shizune Nakamura, Rikuto Goto, Akiko Kubota, Naoaki Sakamoto, Akinori Awazu

This study examines the transcriptomic effects of HDAC inhibitors on feline cells, finding organ-specific responses and differential gene expression patterns compared to human cells.

bioRxiv · Jun 10, 2026 · PreprintCell Biology

Whole-genome sequencing of CRFK and PG-4 cells to infer the phenotype of the original donor cats

Ganma Tanaka, Rikuto Goto, Tetsushi Komoto, Akiko Kubota, Reo Hayashi, Takeshi Igawa, Naoaki Sakamoto, Akinori Awazu

The paper uses whole-genome sequencing of CRFK and PG-4 cells to infer the phenotype of their donor cats, identifying coat and iris color traits.

Companion Animal Health and Genetics · Mar 6, 2026Peer-reviewedGenomics

Common tissue-specific expressions and regulatory mechanisms of c-KIT isoforms with and without GNNK and GNSK sequences across five mammals

Rikuto Goto, Naoaki Sakamoto, Akinori Awazu

The paper analyzes c-KIT isoform expression across five mammals, finding conserved tissue-specific patterns and identifying regulatory factors for alternative splicing.

PLoS ONE · Jan 20, 2026Peer-reviewedBioinformatics