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Current · Arkansas
Last published
2025
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OpenAlex · ORCID
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2026-10-06
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Bohu Pan
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Also affiliated: United States Food and Drug Administration (2017–2025); Chinese Academy of Sciences (2012–2018); Shanghai Institutes for Biological Sciences (2012–2016); Center for Excellence in Molecular Plant Sciences (2012–2018); University of Chinese Academy of Sciences (2018)
16 h-index
54 pubs
1,479 cited
Research Areas
Biomedical Subjects
Links
Biography and Research Information
OverviewAI-generated summary
Bohu Pan's research focuses on utilizing high-throughput sequencing technologies to investigate genetic and molecular mechanisms underlying various biological processes and disease states. Pan has published work examining the reproducibility of variant detection in whole genome sequencing, as well as investigating structural variant detection biases. This work contributes to the understanding of genomic data integrity and analysis methodologies. Pan has also explored the mutagenicity of nanoparticles using whole-genome sequencing in mouse lymphoma cells, indicating an interest in environmental toxicology and its genetic impacts. Further research includes elucidating interactions between SARS-CoV-2 proteins and human receptors using computational modeling and investigating epidemiological traits through sequence analysis. Pan has collaborated with researchers at the National Center for Toxicological Research, including Joe Meehan and Weigong Ge, with whom Pan has co-authored multiple publications.
Metrics
- h-index: 16
- Publications: 54
- Citations: 1,479
Selected Publications
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Augmenting precision medicine via targeted RNA-Seq detection of expressed mutations (2025)
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Targeted DNA-seq and RNA-seq of Reference Samples with Short-read and Long-read Sequencing (2024)
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Clonal hematopoiesis driven by mutated DNMT3A promotes inflammatory bone loss (2024)
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Evaluation of mutagenic susceptibility of different stages in germ cell development of Caenorhabditis elegans using whole genome sequencing (2023)
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Additional file 3 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing (2022)
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Additional file 13 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing (2022)
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Additional file 5 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing (2022)
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Additional file 15 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing (2022)
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Additional file 10 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing (2022)
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Additional file 9 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing (2022)
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Additional file 11 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing (2022)
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Additional file 1 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing (2022)
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Additional file 6 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing (2022)
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Additional file 12 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing (2022)
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Additional file 7 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing (2022)
Collaboration Network
Top Collaborators
Rebecca Kusko
22 shared publications
- Similarities and differences between variants called with human reference genome HG19 or HG38
- Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Structural Changes Due to Antagonist Binding in Ligand Binding Pocket of Androgen Receptor Elucidated Through Molecular Dynamics Simulations
- Computational prediction models for assessing endocrine disrupting potential of chemicals
- Targeted DNA-seq and RNA-seq of Reference Samples with Short-read and Long-read Sequencing
Showing 5 of 22 shared publications
Gökhan Yavaş
National Center for Toxicological Research (US)
18 shared publications
- Persistent Organic Pollutants in Food: Contamination Sources, Health Effects and Detection Methods
- Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Elucidating Interactions Between SARS-CoV-2 Trimeric Spike Protein and ACE2 Using Homology Modeling and Molecular Dynamics Simulations
- Informing selection of drugs for COVID-19 treatment through adverse events analysis
- Additional file 14 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
Showing 5 of 18 shared publications
Chunlin Xiao
National Center for Biotechnology Information (US)
17 shared publications
- Similarities and differences between variants called with human reference genome HG19 or HG38
- Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Correction to: Similarities and differences between variants called with human reference genome HG19 or HG38
- Additional file 14 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 2 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
Showing 5 of 17 shared publications
Fritz J. Sedlazeck
Baylor College of Medicine (US)
16 shared publications
- Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Hidden biases in germline structural variant detection
- Additional file 14 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 2 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 4 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
Showing 5 of 16 shared publications
Andreas Scherer
University of Helsinki (FI)
16 shared publications
- Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Augmenting precision medicine via targeted RNA-Seq detection of expressed mutations
- Additional file 14 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 2 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 4 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
Showing 5 of 16 shared publications
Jonathan Foox
Cornell University (US)
16 shared publications
- Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Augmenting precision medicine via targeted RNA-Seq detection of expressed mutations
- Additional file 14 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 2 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 4 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
Showing 5 of 16 shared publications
Luyao Ren
Fudan University (CN)
15 shared publications
- Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 14 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 2 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 4 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 7 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
Showing 5 of 15 shared publications
Vitor Onuchic
Illumina (United States) (US)
15 shared publications
- Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 14 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 2 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 4 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 7 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
Showing 5 of 15 shared publications
Meijian Guan
SAS Institute (United States) (US)
15 shared publications
- Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 14 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 2 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 4 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 7 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
Showing 5 of 15 shared publications
Steve Bruinsma
Illumina (United States) (US)
15 shared publications
- Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 14 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 2 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 4 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 7 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
Showing 5 of 15 shared publications
Len Trigg
15 shared publications
- Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 14 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 2 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 4 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 7 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
Showing 5 of 15 shared publications
Baitang Ning
National Center for Toxicological Research
15 shared publications
In database
- Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 14 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 2 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 4 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 7 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
Showing 5 of 15 shared publications
Christine Glidewell-Kenney
Illumina (United States) (US)
15 shared publications
- Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 14 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 2 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 4 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 7 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
Showing 5 of 15 shared publications
Eric Donaldson
United States Food and Drug Administration (US)
15 shared publications
- Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 14 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 2 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 4 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 7 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
Showing 5 of 15 shared publications
Gary P. Schroth
Illumina (United States) (US)
15 shared publications
- Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 14 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 2 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 4 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
- Additional file 7 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing
Showing 5 of 15 shared publications
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Based on overlapping research topics
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