Isar Nassiri
University of Oxford
Research areas: Immunology and Microbiology · Immunology · Cancer Immunotherapy and Biomarkers · Immunotherapy and Immune Responses · T-cell and B-cell Immunology
About
I am a Senior Spatial Transcriptomics Computational Biologist at the Oxford-GSK Institute of Molecular and Computational Medicine (IMCM). My core responsibilities are target and biomarker discovery using spatial profiling in neurodegenerative diseases, specifically Parkinson's disease.
I have education and work experience in Genetics (MSc), Bioinformatics (PhD), Computational Biology (postdoc researcher for two years, Microsoft Research - the University of Trento Centre for Computational and Systems Biology in Italy), Biostatistics and Machine Learning (postdoc associate for two years, Department of Biostatistics and Computational Biology, University of Rochester, USA), and Bioinformatics and Statistical Genetics (postdoc associate for four years, Department of Oncology, University of Oxford, UK). I worked as a Senior Bioinformatician and line manager at Oxford Genomics Centre (OGC) for two years and provided appropriate and timely data processing and analysis for the data being generated by OGC.
Employment
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University of Oxford Senior Spatial Transcriptomics Computational Biologist2023 - Present
Education
Education history is unavailable.
Projects & Funding
Projects & funding information is unavailable.
Publications (7)
- Cytomegalovirus infection protects against metastatic melanoma and modulates oncological outcome and toxicity to checkpoint immunotherapy Save
- An isoform quantitative trait locus in SBNO2 links genetic susceptibility to Crohn’s disease with defective antimicrobial activity Save
- Peripheral monocyte transcriptomics associated with immune checkpoint blockade outcomes in metastatic melanoma Save
- Demultiplexing of single-cell RNA-sequencing data using interindividual variation in gene expression Save
- scQCEA: a framework for annotation and quality control report of single-cell RNA-sequencing data Save
- Sensitivity to Immune Checkpoint Blockade and Progression-Free Survival is associated with baseline CD8+T cell clone size and cytotoxicity Save
- EPISPOT: an epigenome-driven approach for detecting and interpreting hotspots in molecular QTL studies Save