Visanu Wanchai
Instructor
Also affiliated: Oak Ridge National Laboratory (2015–2017); Molecular Microbiology and Genomics Consultants (Germany) (2017); Institute for Musculoskeletal Health (2025); Winthrop Rockefeller Foundation (2022–2024); Institute of Informatics of the Slovak Academy of Sciences (2025)
Faculty Researcher
Biomedical Informatics, College of Medicine
Research Areas
Biomedical Subjects
Biography and Research Information
OverviewAI-generated summary
Visanu Wanchai's research focuses on the application of bioinformatics and genomics to understand biological systems. His work includes analyzing bacterial genomes to determine phylogroups, as demonstrated in his publication on Escherichia coli. Wanchai has also investigated methods for identifying extrachromosomal circular DNA using long-read sequencing, contributing to the advancement of molecular biology techniques. His research extends to viral genomics, with studies on the genetic repertoire of SARS-CoV-2 during the COVID-19 pandemic and comparisons of Monkeypox virus genomes. Additionally, Wanchai has explored the genetic underpinnings of diseases such as multiple myeloma, examining immune microenvironment alterations and investigating therapeutic approaches like bispecific CAR-T cells. He also contributes to the study of animal models, refining the identification of cell types associated with bone structures in mice.
Metrics
- h-index: 15
- Publications: 50
- Citations: 1,014
Selected Publications
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Protocol for the enrichment of endosteal and periosteal mesenchymal cells from murine bone for single-cell transcriptome analysis (2026)
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A transcriptomic-driven segmentation and cell simulation framework for high-resolution spatial transcriptomics and cell-cell communication (2026)
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visanuwan/TENGU: V0.1.0 (2026)
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visanuwan/TENGU: V0.1.0 (2026)
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Abstract 2326: Differentiating epigenetic marks and DNA adducts at the KRAS codon 12 mutation hotspot using ONT/ELIGOS sequencing (2026)
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An enhancement of extrachromosomal circular DNA enrichment and amplification to address the extremely low overlap between replicates (2026)
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Elevation of master autophagy regulator Tfeb in osteoblast lineage cells increases bone mass and strength (2025)
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An Enhancement of Extrachromosomal Circular DNA Enrichment and Amplification to Address the Extremely Low Overlap Between Replicates (2025)
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Single Nuclei Multiomic Profiling of Transcriptional and Chromatin Accessibility of Tumor Cells Underlines Extensive Cis-Regulatory Interaction during Multiple Myeloma Progression (2024)
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Multi-Omics Reveal Immune Microenvironment Alterations in Multiple Myeloma and Its Precursor Stages (2024)
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Multi-omics reveal immune microenvironment alterations in multiple myeloma and its precursor stages (2024)
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DNA structural features and variability of complete MHC locus sequences (2024)
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A Risk Stratification System in Myeloma Patients with Autologous Stem Cell Transplantation (2024)
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Refining the identity of mesenchymal cell types associated with murine periosteal and endosteal bone (2024)
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Bispecific BCMA/CD24 CAR-T cells control multiple myeloma growth (2024)
Grants & Funding
As listed on this researcher's institutional profile.
- Center for Musculoskeletal Disease Research (CMDR) NIH/Nat. Inst. of General Medical Sciences Principal Investigator
- Project 1 – Prevention of MGUS progression to MM by modulating the bone marrow microenvironment NIH/Nat. Cancer Institute via Baylor College of Medicine Principal Investigator
Collaboration Network
Top Collaborators
- CReSIL: accurate identification of extrachromosomal circular DNA from long-read sequences
- Native RNA or cDNA Sequencing for Transcriptomic Analysis: A Case Study on Saccharomyces cerevisiae
- Refining the identity of mesenchymal cell types associated with murine periosteal and endosteal bone
- High NEK2 expression in myeloid progenitors suppresses T cell immunity in multiple myeloma
- Two SARS-CoV-2 Genome Sequences of Isolates from Rural U.S. Patients Harboring the D614G Mutation, Obtained Using Nanopore Sequencing
Showing 5 of 11 shared publications
- Bispecific BCMA/CD24 CAR-T cells control multiple myeloma growth
- Multi-omics reveal immune microenvironment alterations in multiple myeloma and its precursor stages
- High NEK2 expression in myeloid progenitors suppresses T cell immunity in multiple myeloma
- A gene signature can predict risk of MGUS progressing to multiple myeloma
- A Risk Stratification System in Myeloma Patients with Autologous Stem Cell Transplantation
Showing 5 of 9 shared publications
- Bispecific BCMA/CD24 CAR-T cells control multiple myeloma growth
- Multi-omics reveal immune microenvironment alterations in multiple myeloma and its precursor stages
- High NEK2 expression in myeloid progenitors suppresses T cell immunity in multiple myeloma
- A gene signature can predict risk of MGUS progressing to multiple myeloma
- A Risk Stratification System in Myeloma Patients with Autologous Stem Cell Transplantation
Showing 5 of 9 shared publications
- Bispecific BCMA/CD24 CAR-T cells control multiple myeloma growth
- Multi-omics reveal immune microenvironment alterations in multiple myeloma and its precursor stages
- High NEK2 expression in myeloid progenitors suppresses T cell immunity in multiple myeloma
- A gene signature can predict risk of MGUS progressing to multiple myeloma
- A Risk Stratification System in Myeloma Patients with Autologous Stem Cell Transplantation
Showing 5 of 8 shared publications
- Bispecific BCMA/CD24 CAR-T cells control multiple myeloma growth
- Multi-omics reveal immune microenvironment alterations in multiple myeloma and its precursor stages
- High NEK2 expression in myeloid progenitors suppresses T cell immunity in multiple myeloma
- A gene signature can predict risk of MGUS progressing to multiple myeloma
- A Risk Stratification System in Myeloma Patients with Autologous Stem Cell Transplantation
Showing 5 of 8 shared publications
- Bispecific BCMA/CD24 CAR-T cells control multiple myeloma growth
- Multi-omics reveal immune microenvironment alterations in multiple myeloma and its precursor stages
- High NEK2 expression in myeloid progenitors suppresses T cell immunity in multiple myeloma
- A gene signature can predict risk of MGUS progressing to multiple myeloma
- A Risk Stratification System in Myeloma Patients with Autologous Stem Cell Transplantation
Showing 5 of 8 shared publications
- Bispecific BCMA/CD24 CAR-T cells control multiple myeloma growth
- Multi-omics reveal immune microenvironment alterations in multiple myeloma and its precursor stages
- High NEK2 expression in myeloid progenitors suppresses T cell immunity in multiple myeloma
- A gene signature can predict risk of MGUS progressing to multiple myeloma
- A Risk Stratification System in Myeloma Patients with Autologous Stem Cell Transplantation
Showing 5 of 8 shared publications
- Bispecific BCMA/CD24 CAR-T cells control multiple myeloma growth
- Multi-omics reveal immune microenvironment alterations in multiple myeloma and its precursor stages
- High NEK2 expression in myeloid progenitors suppresses T cell immunity in multiple myeloma
- A gene signature can predict risk of MGUS progressing to multiple myeloma
- A Risk Stratification System in Myeloma Patients with Autologous Stem Cell Transplantation
Showing 5 of 8 shared publications
- Bispecific BCMA/CD24 CAR-T cells control multiple myeloma growth
- Multi-omics reveal immune microenvironment alterations in multiple myeloma and its precursor stages
- High NEK2 expression in myeloid progenitors suppresses T cell immunity in multiple myeloma
- A gene signature can predict risk of MGUS progressing to multiple myeloma
- A Risk Stratification System in Myeloma Patients with Autologous Stem Cell Transplantation
Showing 5 of 8 shared publications
- Bispecific BCMA/CD24 CAR-T cells control multiple myeloma growth
- Multi-omics reveal immune microenvironment alterations in multiple myeloma and its precursor stages
- High NEK2 expression in myeloid progenitors suppresses T cell immunity in multiple myeloma
- A gene signature can predict risk of MGUS progressing to multiple myeloma
- A Risk Stratification System in Myeloma Patients with Autologous Stem Cell Transplantation
Showing 5 of 8 shared publications
- Bispecific BCMA/CD24 CAR-T cells control multiple myeloma growth
- Multi-omics reveal immune microenvironment alterations in multiple myeloma and its precursor stages
- High NEK2 expression in myeloid progenitors suppresses T cell immunity in multiple myeloma
- A gene signature can predict risk of MGUS progressing to multiple myeloma
- A Risk Stratification System in Myeloma Patients with Autologous Stem Cell Transplantation
Showing 5 of 8 shared publications
- Bispecific BCMA/CD24 CAR-T cells control multiple myeloma growth
- A gene signature can predict risk of MGUS progressing to multiple myeloma
- A Risk Stratification System in Myeloma Patients with Autologous Stem Cell Transplantation
- Multi-Omics Reveal Immune Microenvironment Alterations in Multiple Myeloma and Its Precursor Stages
- A 12 Gene Signature Accurately Predicts Multiple Myeloma Progression from Monoclonal Gammopathy of Undetermined Significance
Showing 5 of 7 shared publications
- Bispecific BCMA/CD24 CAR-T cells control multiple myeloma growth
- Multi-omics reveal immune microenvironment alterations in multiple myeloma and its precursor stages
- A gene signature can predict risk of MGUS progressing to multiple myeloma
- Multi-Omics Reveal Immune Microenvironment Alterations in Multiple Myeloma and Its Precursor Stages
- A 12 Gene Signature Accurately Predicts Multiple Myeloma Progression from Monoclonal Gammopathy of Undetermined Significance
Showing 5 of 7 shared publications
- Bispecific BCMA/CD24 CAR-T cells control multiple myeloma growth
- A gene signature can predict risk of MGUS progressing to multiple myeloma
- A Risk Stratification System in Myeloma Patients with Autologous Stem Cell Transplantation
- A 12 Gene Signature Accurately Predicts Multiple Myeloma Progression from Monoclonal Gammopathy of Undetermined Significance
- A Gene Signature Can Predict Risk of MGUS Progressing to Multiple Myeloma
Showing 5 of 6 shared publications
- Mash-based analyses of Escherichia coli genomes reveal 14 distinct phylogroups
- The first three waves of the Covid-19 pandemic hint at a limited genetic repertoire for SARS-CoV-2
- Comparison of Monkeypox virus genomes from the 2017 Nigeria outbreak and the 2022 outbreak
- Two SARS-CoV-2 Genome Sequences of Isolates from Rural U.S. Patients Harboring the D614G Mutation, Obtained Using Nanopore Sequencing
- DNA structural features and variability of complete MHC locus sequences
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