π Welcome to My GitHub Pages!
π Welcome to My GitHub Pages!
About Me
Hello! Iβm Pedram Torabian, a passionate researcher and data scientist with a strong background in bioinformatics, genomics, and machine learning. Currently pursuing a Master of Medical Science at the University of Calgary, I leverage my expertise in R, Python, and high-performance computing to analyze complex biological data. My work focuses on spatial transcriptomics, single-cell RNA sequencing (scRNA-seq), and deploying machine learning techniques to uncover insights in cancer research and other genetic disorders.
π± My Journey
From the early days of my academic career, I immersed myself in the fascinating realms of genetics and molecular biology. Earning my Master of Human Genetics from Iran University, I delved deep into genetic disorders, population genetics, and advanced topics in human genetics. This foundation paved the way for my pursuit of a Master of Medical Science at the University of Calgary, where I honed my skills in bioinformatics and applied genomics.
Throughout my career, Iβve had the privilege of working with esteemed institutions like the Arnie Charbonneau Cancer Institute and the Alberta Machine Intelligence Institute (Amii). At the Cancer Institute, I spearheaded projects that integrated machine learning with spatial transcriptomics and single-cell RNA sequencing data, developing classifiers that predict cell identities with remarkable accuracy. My role at Amii involved creating educational content for AI applications in biology, bridging the gap between complex scientific concepts and accessible learning materials.
π οΈ Technical Skills
- Programming Languages: R, Python, Bash, Git
- Data Analysis: Spatial Transcriptomics, Single-cell RNA-seq, Bulk RNA-seq
- Machine Learning: Supervised & Unsupervised Techniques, XGBoost
- Statistical Analysis: Kruskal-Wallis Test, Mann-Whitney U Test, ANOVA
- Bioinformatics Tools: Seurat, CellPhoneDB, CellChat, DESeq2, Monocle3, ssGSEA, GSVA
- High-Performance Computing: Slurm for managing compute jobs on HPC clusters
π Education
Master of Medical Science
University of Calgary
July 2020 β October 2024
GPA: 3.7/4.0
- Key Courses: Intro Bioinformatics Resources, Advanced Bioinformatics, Tumor Microenvironment Dynamics, Intro Biostat Methods, Applied Genomics, Tumor Immunology and Therapy
Master of Human Genetics
Iran University
September 2013 β February 2016
GPA: 3.5/4.0
- Key Courses: Genetics Engineering, Advanced Topics in Human Genetics, Population Genetics
πΌ Professional Experience
Content Development Support - Educational Product
Alberta Machine Intelligence Institute (Amii)
April 2024 β June 2024
- Created educational content for the βUsing AI in Biology & Life Sciencesβ MOOC, enhancing the learning experience for students and professionals.
Research Assistant
Arnie Charbonneau Cancer Institute, University of Calgary
July 2020 β Present
- Machine Learning Classifier Development: Developed a comprehensive classifier in R and Python for spatial transcriptomics data analysis, utilizing seven algorithms including XGBoost to accurately predict non-annotated cell identities based on differentially expressed genes.
- Statistical Analysis: Conducted analyses using Kruskal-Wallis, Mann-Whitney U, and ANOVA tests.
- Single-Cell Analysis: Utilized tools such as CellPhoneDB and CellChat for cell communication studies, DESeq2 for gene expression analysis, Monocle3 for pseudotime analysis, and ssGSEA with GSVA.
- Data Integration: Analyzed 30 GB of scRNA-seq data from ten samples using Seurat, identifying cell type-specific marker genes and compiling a comprehensive marker gene list.
- Bulk RNA-seq Deconvolution: Applied computational deconvolution methods to bulk RNA-seq data from 180 pancreatic cancer samples in TCGA, uncovering gene expression dynamics related to stromal levels in the tumor microenvironment.
Research Assistant
Razavi Hospital, Iran
November 2016 β October 2019
- Led a genetic generalized epilepsy project, advancing familial genetic profiling and contributing to key research publications.
- Authored a comprehensive review on genetic and epigenetic aspects of Celiac disease.
- Investigated primary non-Hodgkinβs lymphoma in atypical sites, providing insights into extra-lymphatic lymphoma detection and treatment.
Research Assistant
Iran University
September 2013 β February 2016
- Led five research projects on genetic disorders including long-QT syndrome, breast cancer, glioblastoma, and Celiac disease.
- Utilized statistical analysis, proteomics, qPCR, and academic writing to guide strategic direction and execution.
Molecular Biologist and Stem Cell Intern
November 2011 β May 2012
- Mastered laboratory techniques in molecular biology and stem cell biology, including RT-PCR and cell culture.
π Awards & Achievements
-
π Griffith University Postgraduate Research Scholarship (GUPRS)
Awarded $28,092 AUD β December 2019 -
π₯ Top 2% Ranking
Among participants in the national masterβs level entrance exam β September 2013 -
π₯ Top 1% Ranking
Nationwide in the Iran national entrance exam β September 2008
π Featured Projects
Machine Learning Classifier for Spatial Transcriptomics
Developed a robust machine learning classifier in R and Python to analyze spatial transcriptomics data, accurately predicting cell identities based on gene expression profiles. Utilized algorithms like XGBoost and integrated Seurat for data analysis.
Single-Cell RNA-seq Data Integration
Led the analysis of 30 GB of single-cell RNA-seq data from ten samples using Seurat, identifying cell type-specific marker genes and compiling a comprehensive marker gene list for diverse cellular population detection.
Computational Deconvolution of Bulk RNA-seq Data
Applied four computational deconvolution methods to bulk RNA-seq data from pancreatic cancer samples in TCGA, uncovering gene expression variations related to stromal levels in the tumor microenvironment, providing insights into cancer progression.
π GitHub Stats
π« Get in Touch
Iβm always open to discussing innovative research, collaborations, or new opportunities. Feel free to reach out via: