Author

Teruhiko Yoshida

National Cancer Center HospitalORCID 0000-0003-1607-3899Unclaimed ORCID profile · follow to get notified of new preprints

Additional preprints under this name without ORCID

Teruhiko Yoshida1 paper · National Cancer Center Research Institute

Biology Disciplines

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Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Research Focus:variant calling· 2 Research Focus:differential expression· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Research Focus:polygenic risk· 1 Approach:statistical model· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Makoto HirataiD· 2 shared Noriko TanabeiD· 2 shared Satoyo Oda· 2 shared Ai OkadaiD· 1 shared Chikako TomozawaiD· 1 shared Hiromi Sakamoto· 1 shared Katsushi TokunagaiD· 1 shared Kenichi ChibaiD· 1 shared

Activity by Year

2023-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 35 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Makoto HirataORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintMay 29, 2025

A germline and somatic mutation sorting (GeMSort) algorithm for extracting presumed germline pathogenic variants in liquid genomic profiling: Insights from Database of Center for Cancer Genomics and Advanced Therapeutics (C-CAT)

Satoyo Oda, Manami Matsukawa, Chikako Tomozawa…·Makoto Hirata

The paper develops a GeMSort algorithm to accurately distinguish germline from somatic variants in liquid biopsy genomic profiling using real-world data from over 11,000 patients.

DOI 10.1101/2025.05.29.25327892

humanwhole-exome sequencing

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Genetic & Genomic MedicinemedRxivPreprintMay 30, 2023

A comprehensive workflow for target adaptive sampling long-read sequencing applied to hereditary cancer patient genomes

Wataru Nakamura, Makoto Hirata, Satoyo Oda…·Yuichi Shiraishi

This study develops a computational workflow for target adaptive sampling long-read sequencing and applies it to hereditary cancer genomes to identify genetic variants and epigenetic changes.

7 citations

humanwhole-genome sequencing

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