Valentin Dinu
· Associate ProfessorArizona State University · Biomedical Diagnostics
Active 2006–2024
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About
Valentin Dinu is an Associate Professor at the College of Health Solutions at ASU, directing the Translational Bioinformatics Lab. He holds a PhD in Computational Biology and Bioinformatics from Yale University and an A.B. in Mathematics and Physics from Harvard University. His research focuses on developing informatics methods and applications for managing, integrating, and analyzing large biomedical datasets generated through high-throughput platforms such as genomic sequencing, microarrays, and mass spectrometry. His work has been applied to analyze data related to various diseases, including cancer, diabetes, obesity, Alzheimer’s disease, schizophrenia, and age-related macular degeneration. Professor Dinu's research aims to facilitate the management, integration, and analysis of diverse biomedical information sources by improving computational approaches, software applications, and databases. He has contributed to the use of biological domain knowledge to enhance statistical analysis and data mining methods for disease gene and pathway identification, as well as exploring database modeling approaches for large, heterogeneous datasets from clinical and biosciences domains. His research has been supported by multiple agencies, including NIH, BARDA, DOD, VA, and others, and he has mentored numerous scientists across various career stages, many of whom have gone on to successful careers in industry, healthcare, research institutes, and academia.
Research topics
- Biology
- Genetics
- Immunology
- Computational biology
- Medicine
- Cancer research
- Evolutionary biology
- Botany
Selected publications
Virus Research · 2020 · 92 citations
Senior authorCorrespondingScientific Reports · 2020 · 46 citations
To further understand the molecular pathogenesis of desmoplastic small round cell tumor (DSRCT), a fatal malignancy occurring primarily in adolescent/young adult males, we used next-generation RNA sequencing to investigate the gene expression profiles intrinsic to this disease. RNA from DSRCT specimens obtained from the Children's Oncology Group was sequenced using the Illumina HiSeq 2000 system and subjected to bioinformatic analyses. Validation and functional studies included WT1 ChIP-seq, EWS…
Metabolism · 2018-09-22 · 28 citations
articleBehavior Genetics · 2019-04-04 · 27 citations
articleAccurate Identification of Subclones in Tumor Genomes
Molecular Biology and Evolution · 2022 · 13 citations
Understanding intratumor heterogeneity is critical for studying tumorigenesis and designing personalized treatments. To decompose the mixed cell population in a tumor, subclones are inferred computationally based on variant allele frequency (VAF) from bulk sequencing data. In this study, we showed that sequencing depth, mean VAF, and variance of VAF of a subclone are confounded. Without considering this effect, current methods require deep-sequencing data (>300× depth) to reliably infer subclone…
Frequent coauthors
- 10 shared
Margaret Linan
Icahn School of Medicine at Mount Sinai
- 9 shared
Jean-Pierre A. Kocher
WinnMed
- 9 shared
Michael A. Meiners
Mayo Clinic
- 9 shared
David A. Rider
- 9 shared
Asif Hossain
- 9 shared
Venkata D. Yellapantula
- 9 shared
Patrick E. Duffy
Mayo Clinic
- 9 shared
Steven N. Hart
University College London
Labs
Education
Ph.D., Computational Biology and Bioinformatics
Yale University
Other, Mathematics and Physics
Harvard University
Awards & honors
- Excellence in Teaching Award (1999)
- Magna Cum Laude with Highest Honors college graduate (2000)
- PhD funded by National Library of Medicine Biomedical Inform…
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