I provide advanced bioinformatics consulting for cancer epigenomics and multi-omics research projects. My expertise includes ChIP-seq, RNA-seq, enhancer/super-enhancer identification, transcription factor analysis, and integrative regulatory genomics. With hands-on experience analysing large-scale datasets (including multi-condition tumour cohorts), I offer complete end-to-end computational workflows — from raw FASTQ files to publication-ready figures and statistical interpretation. Core Expertise: • ChIP-seq analysis (H3K27ac, H3K4me3, BRD4, TF ChIP)• Super-enhancer identification (ROSE pipeline, peak stitching, TSS filtering)• Enhancer/promoter classification and annotation• RNA-seq differential expression analysis• Multi-omics integration (ChIP-seq + RNA-seq)• Transcription factor enrichment and network analysis• Heatmaps, meta-profiles, signal density plots• Survival analysis (SPSS / R)• Reproducible pipelines (Linux, deepTools, MACS2, R, Python) What You Will Receive: • Clean, reproducible analysis pipeline• Publication-quality figures (heatmaps, volcano plots, survival curves, GSEA plots)• Well-annotated scripts• Statistical interpretation• Guidance for manuscript preparation This service is ideal for PhD students, clinicians, and researchers working in oncology, epigenetics, or translational medicine.