I am a bioinformatician and Python/R developer with 5+ years of experience processing NGS datasets and developing analytical workflows. Co-author of 15 peer-reviewed publications (Genome Medicine, Epigenetics & Chromatin).
Services:
- NGS Data Analysis: WGS/WES (GATK, SNP prioritization, variant calling), RNA-seq (DESeq2), ChIP-seq (ChIPseeker), and Hi-C/Exo-C (Juicer, Juicebox).
- Bioinformatics Scripting: Custom scripts and pipeline development in Python (pandas, NumPy, scikit-learn) and R (Bioconductor).
- Tooling & Environments: BLAST, BWA, Bowtie2, SAMtools, Picard, Docker, Conda, Bash.
- Data Visualization: Publication-ready figures using Matplotlib, Seaborn, Plotly, and ggplot2.
Deliverables:
- Processed sequence data and variant files (VCF, BAM, BED, count matrices).
- Clean, documented code and reproducible environment setups.
- Summary reports with figures and data interpretations.
Please contact me before placing an order to discuss your data structure and project requirements.