Next-Generation Sequencing
& Research Services
Powered by Illumina NextSeq 1000 and iSeq 100. Comprehensive genomic analysis from whole genome sequencing to bioinformatics — all in Nairobi.
NGS Sequencing Services
Comprehensive genomic analysis powered by Illumina technology
Whole Genome Sequencing
Complete genome analysis for research and clinical applications.
- Complete genomic coverage
- Structural variant detection
- Research & clinical grade
Whole Exome Sequencing
Targeted exome capture for efficient variant discovery.
- Protein-coding region focus
- Cost-effective variant discovery
- High coverage depth
RNA Sequencing / Transcriptomics
Gene expression profiling and transcriptome analysis.
- Differential expression analysis
- Novel transcript discovery
- Splice variant detection
Clinical Panels
Cancer diagnostics and pharmacogenomics panels.
- Oncology gene panels
- Pharmacogenomics profiling
- Actionable mutation reporting
16S/18S/ITS Metagenomics
Microbial community profiling for research.
- Bacterial & fungal profiling
- Community diversity analysis
- Taxonomic classification
Targeted Sequencing
Focused cancer research and mutation detection.
- Custom gene panels
- Somatic mutation detection
- Ultra-deep sequencing
Run-only Sequencing
Bring your pre-made library, we run the sequencing. Ideal for labs with in-house library preparation capabilities.
- Your library, our platform: NextSeq 1000 or iSeq 100
- Flexible: Any compatible library type accepted
- Fast turnaround: Sequencing data delivered promptly
Not sure which service fits your research?
Discuss your project with usBioinformatics Services
Expert analysis pipelines to turn your sequencing data into actionable insights
Variant Calling
SNP and indel identification with industry-standard GATK and FreeBayes pipelines.
Genome Assembly
De novo and reference-guided genome assembly for novel organisms and strains.
Gene Expression Analysis
Differential expression, pathway enrichment, and functional annotation from RNA-seq data.
Transcriptome Assembly
Full-length transcript reconstruction and isoform characterization from RNA sequencing.
Taxonomical Classification
Microbial identification and community composition analysis from metagenomic data.
Custom Analysis
Bespoke bioinformatics pipelines tailored to your specific research questions and data types.
How It Works
From consultation to results — a streamlined workflow
Consultation
Discuss your research needs and project requirements with our team.
Sample Submission
Send samples or pre-made libraries to our facility in Nairobi.
Results & Analysis
Receive sequencing data and comprehensive bioinformatics reports.
Co-working Laboratory Space
Our co-working laboratory space provides researchers access to state-of-the-art NGS equipment and bioinformatics workstations.
- NGS Equipment Access: Hands-on use of Illumina NextSeq 1000 and iSeq 100 platforms.
- Bioinformatics Workstations: High-performance computing resources for data analysis.
- Flexible Arrangements: Short-term and long-term co-working options available for researchers and institutions.
Why Partner with CA Medlynks?
Kenya's leading genomics facility for research institutions and scientists
First NGS in Kenya
Pioneering next-generation sequencing services in Kenya — eliminating the need to send samples abroad.
Illumina Platforms
State-of-the-art NextSeq 1000 and iSeq 100 instruments for high-throughput and targeted sequencing.
Expert Bioinformaticians
Experienced bioinformatics scientists providing end-to-end data analysis and custom pipelines.
Fast Turnaround
Efficient workflows and local processing mean faster results compared to sending samples overseas.
Co-working Lab Space
On-site laboratory access for researchers who prefer hands-on work with our NGS equipment.
Competitive Pricing
Affordable rates for institutions and researchers across Africa — significant savings versus international labs.
What Our Partners Say
Trusted by researchers and institutions across Kenya
"No queue, no hassle, no too much paper work. Staffs are nice and efficient. The result will be sent to your email address in few hours."
"Place is first class. If you are a local or a foreigner I recommend you come here."
"The process was pretty much smooth, good customer service and the results were delivered as they said they would within 8 hours."
Our Location
Visit our genomics facility in the heart of Nairobi
Daykio Plaza
Ground Floor, Off Ngong Lane, Nairobi
Mon-Fri: 8AM - 8PM | Sat: 8AM - 5PM
Get DirectionsFrequently Asked Questions
What NGS platforms do you use?
We use Illumina NextSeq 1000 and iSeq 100 for our sequencing services. These platforms provide high-throughput, accurate sequencing suitable for a wide range of genomic applications.
Can I bring my own library for sequencing?
Yes, we offer run-only sequencing where you provide pre-made libraries and we handle the sequencing. This is a cost-effective option for labs that have in-house library preparation capabilities.
Do you provide bioinformatics support?
Yes, we offer comprehensive bioinformatics including variant calling, genome assembly, gene expression analysis, and custom pipelines. Our expert bioinformaticians work with you to ensure your data is analyzed to the highest standards.
Is co-working lab space available?
Yes, we offer co-working laboratory space with access to our NGS equipment and bioinformatics workstations. Both short-term and long-term arrangements are available for individual researchers and institutions.
How do I get a quote?
Contact us via WhatsApp or email with your project details, and we'll provide a customized quote. You can also fill out the form below to request a quote directly.
Related Services
Explore our other diagnostic services
Ready to Start Your Project?
Get in touch with our team for a customized quote tailored to your research needs.
Learn more on our Health Resources blog