My research follows clinical questions into microbiology, genetics, and tissue biology. My thesis adds a wider view: how genomes relate to human history and environmental change.

Related public engagement: Oita Glocal feature on science, education, and regional collaboration.

Projects at a glance

Four questions, four kinds of evidence

Diagram of Geneformer in silico gene perturbation
Tissue to modelGeneformer perturbation in SCLC T cells. Repository.
H. pylori antimicrobial resistance profile from Almaty
Clinic to microbeH. pylori resistance in Almaty. Repository.
Kisaburo Ohara's 1904 satirical map of Europe and Asia
Genome to riskPolygenic scores across ancient and present day populations. Map: Ohara, 1904, public domain. Repository.
Sea turtle among coral at Aka Island, Okinawa
Environment to genomeTransposable elements under ocean acidification, Aka Island fieldwork. Repository.
01

Tissue to model

Digital Pathology and In Silico Gene Perturbation

At Hokkaido University I work with whole slide images and spatial biology in small cell lung cancer. I use Geneformer to predict how deletion or overexpression of one gene changes an SCLC T cell representation. The model can point to a candidate regulator. It cannot prove that the gene controls the cell. I test whether the signal holds across donors and whether tissue evidence supports it.

whole slide imagingspatial biologyGeneformerin silico perturbationT cell statesdonor aware evaluation
See how I check donor consistency
Python excerptdonor_consistency.py

The analysis groups predicted shifts by donor, then checks whether each donor points in the same direction as the full result.

cells["shift"] = shifts
by_donor = cells.groupby("individual")["shift"].agg(["mean", "count"])
overall_mean = float(np.mean(shifts))
overall_sign = np.sign(overall_mean)
same_sign = np.sign(by_donor["mean"]) == overall_sign
Read the source in GitHub

View the current Geneformer T cell work

02

Clinic meets microbiology

Infectious Diseases and Host Pathogen Dynamics

My Helicobacter pylori work starts with patients in Kazakhstan, a common primary care problem. I connect clinical records with culture, epidemiology, and antimicrobial resistance. That local evidence can sharpen regional surveillance and first line treatment decisions.

H. pyloriantimicrobial resistanceclinical microbiologyclinical epidemiologyprimary care

Open the analysis repository · Read the 2026 study

03

Clinical practice · Care to evidence

Clinical Practice and Evidence

General practice taught me to work with incomplete information. It also taught me that an elegant analysis is useless if it does not fit real care. I carry that lesson into research on primary care, infectious disease, palliative care, cancer genetics, and immune disease. Read more about my clinical practice.

general practiceprimary carepalliative careclinical researchstudy designmultidisciplinary care
04

Genome to risk

Polygenic Risk Score Pipelines

I compare polygenic scores across ancient and present day populations. The hard part is not producing a score. It is handling variants clearly and judging whether an effect estimate can travel across ancestry and time.

polygenic scorespopulation genomicsancient DNARreproducibility
See how the score is calculated
R excerptpgs_calculator_1402snps.R

The script matches each observed allele to its reported effect allele, collects the matching effects, and sums them for each person.

for (v in 1:nrow(df2)) {
  trial1 <- as.matrix(as.character(df2[v, ]))
  picker1 <- which(trial1 == ref_test1)
  effect_subject1 <- ref_effect1[picker1]

  snp_count1 <- length(picker1)
  effector1 <- sum(effect_subject1)
}
Read the source in GitHub

Open the Ancient Intelligence repository

05

Model to mechanism

Machine Learning and Bioinformatics

I write workflows that another researcher can inspect and rerun. I document the inputs, the evaluation boundary, and the failures. Speed helps. Biological meaning matters more.

PythonRRNA sequencingGeneformerworkflow validation

Doctoral research · Environment and gene expression

Transposable elements in a changing ocean

My thesis examined 72 brain transcriptomes from Acanthochromis polyacanthus, a coral reef damselfish. The dataset compared control, acute, developmental, and transgenerational carbon dioxide exposure, with offspring from tolerant and sensitive parents.

I examined TE related transcripts alongside broader gene expression patterns. The work suggests questions about genome regulation and brain plasticity that need further investigation. Transcript abundance alone does not establish transposition or a regulatory mechanism.

Explore the public figures and evidence ↗
Read the thesis record ↗

Aka Island reef field context
Field context from Okinawa. The experimental dataset came from laboratory reared fish with parents collected near Palm Island, Australia.

People and places

Research is a team sport

Collaborators and mentors across Kazakhstan, Japan, Australia, and the United States.

Current base

Hokkaido University

Postdoctoral research in digital pathology, whole slide imaging, genomics, bioinformatics, and translational medicine.

Clinical and regional collaboration

Kazakhstan and Japan

Clinical research and infectious-disease partnerships connect patient questions with microbiology and epidemiology.

Field and methods

OIST and international teams

Marine fieldwork and computational collaborations keep samples, methods, and interpretation connected.

Group photograph from the 46th Glocal Infectious Diseases Research Seminar at Oita University in 2026
Oita, 202646th Glocal Infectious Diseases Research Seminar, Oita University. Seminar report.
Students from Saeki Kakujo High School visiting OIST in 2023
OIST, 2023SEED programme visit by Saeki Kakujo High School. Photo © OIST, CC BY 4.0.
A calico cat resting on a wooden deck above the sea at Aka Island, with green hills behind
Field station, supervisedThe resident cat at the Aka Island field station, where the reef fish work was done.

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