How We Work
This section is managed and supervised by a specialist in bioinformatics and medical genetics, ensuring high-quality analysis and scientific accuracy.
Bioinformatics & NGS Data Analysis Services
Transform Your Raw Biological Data Into Clear, Actionable Insights
Modern genomic technologies generate massive amounts of data — but turning that data into meaningful biological or clinical conclusions requires expertise, powerful tools, and a reliable workflow.
On this page, we offer end-to-end bioinformatics and biological data analysis services designed for researchers, clinicians, laboratories, and biotech startups.
Tools & Skills
- Languages: Python, R, Bash
- Platforms: Linux, Galaxy, IGV, Bioconductor
- Tools: FastQC, BWA, STAR, Samtools, GATK, DESeq2, OptiType
- Databases: Ensembl, UCSC, ClinVar, IMGT/HLA, KEGG
Why Work With Us?
- 3+ years of practical experience in bioinformatics & clinical genomics
- Accurate, fast, and well-documented results
- Clear communication throughout all project steps
- Strict confidentiality and secure data handling
- Customized workflows designed specifically for your dataset and goals
Before You Order:
Please contact us with a short description of your project, including:
- Data type (NGS, RNA-Seq, DNA-Seq, FASTQ, VCF, etc.)
- Project goals
- Number of samples / dataset size
- Deadline or timeline
I will review your information and provide a customized plan, estimated delivery time, and recommended workflow.
Let's Turn Your Data Into Discovery
Whether you're conducting research, running a clinical study, or building a biotech product, I can help you extract accurate and meaningful insights from your biological data.
Contact us to get started.
What We Offer
Comprehensive bioinformatics services for research and clinical applications
Next-Generation Sequencing (NGS) Analysis
Comprehensive processing and analysis of FASTQ files, including:
- Quality control & trimming (FastQC, Trimmomatic)
- Read alignment (BWA, HISAT2, STAR)
- Variant calling (GATK, FreeBayes, Samtools)
- Variant annotation (ClinVar, dbSNP, Ensembl, KEGG)
RNA-Seq / Transcriptomics Analysis
Advanced gene expression analysis for research and clinical projects:
- Differential expression (DESeq2, edgeR)
- Clustering and sample similarity analysis
- Gene ontology & pathway enrichment
- Publication-ready heatmaps, volcano plots, PCA
HLA Typing
Accurate allele identification for immunology, transplantation, and clinical studies:
- OptiType
- HLA-VBSeq
- NGSengine
Clinical Genomics & Variant Interpretation
Interpretation and classification of genetic variants using trusted databases:
- ClinVar, dbSNP, Ensembl, HGMD*
- Gene panel analysis (cancer, inherited disorders, screening panels)
- Pharmacogenomics insights
- *Use of HGMD depends on project licensing availability
Custom Bioinformatics Pipelines
Development of fully tailored workflows using:
- Python, R, Bash
- Bioconductor ecosystem
- Linux-based analysis environments
- Galaxy workflows
- Ideal for labs, research groups, and biotech teams with unique needs
Scientific Visualization & Reporting
High-quality outputs ready for publication or presentation:
- Heatmaps
- Volcano plots
- PCA
- Summary tables
- All reports delivered in PDF, HTML, or Markdown