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hani-sabaie/README.md

👋 Hi, I’m Hani

Genetics Computational Genomics Integrative Genomics Single Cell Causal Genomics CNV

R Linux Git Markdown Python Machine Learning


🧬 Human Genetics | Computational Genomics | Integrative Genomics
🎓 M.Sc. in Human Genetics


🔭 I’m currently working on integrative analyses of single-nucleus multi-omics data to investigate cell-type-specific regulation in complex human diseases. In parallel, I apply causal genomics approaches (Mendelian randomization and SMR/HEIDI) and copy number variation (CNV) / structural variant analyses to capture multi-layered genetic contributions to disease susceptibility.

🤝 I’m interested in collaboration on single-cell multi-omics, gene regulatory network analysis, CNV and structural variant interpretation, and causal inference in human genetics.

🌱 I’m currently learning Python programming, machine learning concepts, and advanced Git workflows, alongside computational approaches for integrative analysis of genomic and single-cell data.

🎯 I am actively seeking a PhD position in genomics, bioinformatics, or computational biology, with a focus on single-cell biology, statistical genetics, structural variation, and disease mechanisms.

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  1. mtDNACN-MSP-MR mtDNACN-MSP-MR Public

    Interactive HTML report providing detailed results from a published bidirectional two-sample Mendelian randomization study of mitochondrial DNA copy number and multiple sclerosis progression.

    HTML

  2. LTL-MSP-MR LTL-MSP-MR Public

    Interactive HTML report providing detailed results from a published bidirectional Mendelian randomization study on leukocyte telomere length and multiple sclerosis progression.

    HTML

  3. SCZ-ceRNA-Analysis SCZ-ceRNA-Analysis Public

    R scripts for transcriptomic and ceRNA network analyses in schizophrenia.

    R