Steven Pastor
Bioinformatics Scientist Iii @Children's Hospital of Philadelphia
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WORK HISTORY
Bioinformatics Scientist Iii @Children's Hospital of Philadelphia
EDUCATION
Drexel University School of Biomedical Engineering, Science and Health Systems
Doctor of Philosophy, Bioengineering and Biomedical Engineering
University of New Orleans
Master of Science (MS), Molecular Biology
University of New Orleans
Bachelor of Science (BS), Biology/Biological Sciences, General
SKILLS
ABOUT STEVEN PASTOR
BS Biology, MS Biology (Molecular), PhD Biomedical EngineeringCore Competencies: Structural Biology & Proteomics: AlphaFold • PyMOL • ChimeraX • MSFragger (via FragPipe) • DIA-NN • Spectronaut • PTM discovery • HLA-binding prediction • variant-to-structure pipelines Multi-omics & Sequencing: WGS/WES (Illumina) • Long-read (ONT/PacBio) • Optical mapping • scRNA-seq • scATAC-seq • CITE/TCR-seq • Spatial transcriptomics (Visium, Visium HD, Xenium) Software Engineering: Python package development • CI/CD (GitHub Actions) • Docker/Singularity • Nextflow/Snakemake • SQL (DuckDB/Postgres) • REST APIs • Rust Machine Learning: transformer & embedding models • graph-based regulatory inference • clustering & dimensionality reduction • peptide presentation scoring Translational Impact: neoantigen & peptide discovery • structural variant interpretation • biomarker identification • clinical cohort integration • rare disease genomicsProfessional ExperienceComputational scientist driving multi-omics, structural, and proteogenomic analysis pipelines across oncology and rare disease programs. Developed structural proteogenomics pipeline integrating AlphaFold, MSFragger, DIA-NN, and HLA-binding models to identify non-canonical peptides from RNA-seq, WGS, and mass spec; implemented modular Python framework with automatic QC, CLI tooling, and containerized execution. Led multi-omics analyses of CAR T cell persistence using scRNA-seq, scATAC-seq, CITE-seq, and spatial transcriptomics, uncovering cell state dynamics linked to treatment response. Architected long-read + optical mapping hybrid assembly workflows resolving structural variation in complex genomic regions (22q11.2, subtelomeres), reducing misassembled contigs by >40% and enabling population-scale discovery. Led integrative single-cell & spatial programs (Visium HD) to map tumor microenvironment remodeling in neuroblastoma treatment cohorts, identifying cell state shifts linked to therapy response. Built enterprise reproducible Nextflow pipelines for immunopeptidomics, RNA-seq, and long-read assembly used across multiple labs and HPC environments (Slurm), including automated cloud deployment. Developed full-stack analytical platforms using Flask/Django, React, FastAPI, and Shiny enabling real-time genomic interpretation and multi-omics data visualization for collaborators and clinicians. Drove independent research direction including study design, statistical modeling, computational method selection, and cross-functional communication with clinicians and wet-lab scientists.
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