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DrSeed/README.md

Hi there 👋

I'm Saheed Adeyanju, a UK-based bioinformatician specialising in computational cancer biology, ovarian cancer genomics, and multi-omics integration. I build reproducible next-generation sequencing (NGS) pipelines and apply machine learning to biomarker discovery, bridging computational analysis with a strong molecular-biology background. I hold an MSc in Bioinformatics with Advanced Practice (Distinction, Teesside University), with research experience at Imperial College London and the University of Southampton, and ten peer-reviewed publications and preprints across cancer genomics, multi-omics, and ML in genomics.

Programming Languages

Proficient in Python, R, and Bash (shell scripting), plus Nextflow for pipeline development and SQL for data querying. Comfortable working on HPC clusters and Linux/Unix server environments.

Tech Stack

  • Pipeline development & NGS data analysis

    • Built reproducible Nextflow pipelines based on nf-core/Sarek for somatic variant calling and annotation on ovarian cancer whole-genome sequencing (WGS) data, with containerised GATK, Mutect2, SnpEff, and VEP.
    • Experienced across WGS, WES, bulk RNA-seq, single-cell RNA-seq (scRNA-seq), and microarray data, using Docker and Git/GitHub for reproducible, auditable workflows.
    • Computed homologous recombination deficiency (HRD) scores loss of heterozygosity (LOH), telomeric allelic imbalance (TAI), and large-scale state transitions (LST) to quantify genomic instability and support precision-oncology decisions.
  • Machine Learning

    • Benchmarked machine-learning algorithms (Random Forest, XGBoost, CatBoost, SVM, Logistic Regression, K-means) for biomarker discovery, including identifying candidate biomarkers of Pulmonary Arterial Hypertension from microarray data.
    • Applied dimensionality reduction (PCA, t-SNE, UMAP) and deep-learning frameworks (TensorFlow, PyTorch) to genomic and clinical datasets.
  • Biological network analysis

    • Constructed protein–protein interaction networks in STRING/Cytoscape, extracted hub genes with CytoHubba (e.g. CXCL9), ran functional enrichment with EnrichR, and performed cross-platform meta-analysis with MetaVolcanoR.
    • Validated candidate-gene druggability through molecular docking (AutoDock Vina).

Biology Background

A strong foundation in molecular biology and clinical science — an MSc in Chemical Pathology (University of Ibadan) and a BSc in Biochemistry (Federal University of Agriculture, Abeokuta) — underpins my computational work, alongside several years of research spanning cancer genomics, respiratory disease, and inflammation.

Selected Publications

  • Adeyanju, S. A. & Ogunjobi, T. T. (2024). Machine Learning in Genomics: Applications in WGS, WES, Single-Cell Genomics, and Spatial Transcriptomics. Medinformatics.
  • Adeyanju, S. (2024). Exploring Inflammatory Dysregulation in Alveolar Macrophages: Implications for Novel Therapeutic Targets in COPD. bioRxiv.
  • Adeyanju, S. A. et al. Artificial Intelligence in Autoimmune Disease Genomics: Biomarker Discovery and Pathway Analysis in Multiple Sclerosis. (Accepted, Int. J. Advanced Biological and Biomedical Research.)

How To Reach Me

Fun Facts

  • 🗣️ I speak Yoruba natively and English (IELTS Academic 7.5).
  • 🧬 Member of several research communities, including the European Association for Cancer Research, the African Society of Human Genetics, and the Association for Single Cell Analysis (ASCA).
  • 🎓 Former STEM tutor — I still enjoy explaining tricky computational-biology ideas in plain language.

Pinned Loading

  1. Projects Projects Public

    Jupyter Notebook

  2. single_cell_rna_Seq_analysis single_cell_rna_Seq_analysis Public

    HTML

  3. biomarker-prediction-using-machine-learning biomarker-prediction-using-machine-learning Public

    Jupyter Notebook

  4. fastq-quality-control-toolkit fastq-quality-control-toolkit Public

    Reproduce the classic FASTQ QC plots (read length, per-base quality, GC, barcode frequency) as pure-Python one-liners.

    Python

  5. gwas-manhattan-real-sumstats gwas-manhattan-real-sumstats Public

    Build a Manhattan plot and QQ plot from real GWAS summary statistics (EBI GWAS Catalog) with genomic-inflation lambda.

    Python

  6. negative-binomial-rnaseq-counts negative-binomial-rnaseq-counts Public

    Why RNA-seq counts are negative-binomial not Poisson: overdispersion, the mean-variance trend, and the zero-inflation myth.

    Python