Research Services & NGS

Advanced Next-Generation Sequencing and bioinformatics for researchers and institutions.

CA Medlynks NGS research laboratory with Illumina sequencing equipment

Pioneering Genomics in Kenya

CA Medlynks is one of the early adopters of Next-Generation Sequencing (NGS) in Kenya. Using Illumina NextSeq 1000 and iSeq 100 platforms, we deliver cutting-edge genomic analysis for research institutions, hospitals, and pharmaceutical companies.

Illumina NextSeq 1000 Illumina iSeq 100

NGS Sequencing Services

Comprehensive next-generation sequencing solutions powered by Illumina technology.

Whole Genome Sequencing

Complete DNA sequencing for comprehensive genomic analysis, variant discovery, and population studies.

Whole Exome Sequencing

Targeted sequencing of protein-coding regions for efficient identification of disease-causing mutations.

Whole Transcriptome / RNA Sequencing

Gene expression profiling and transcriptome analysis for understanding cellular function and disease mechanisms.

Clinical Panels

Targeted clinical panels for cancer diagnostics, hereditary disease screening, and pharmacogenomics applications.

16S/18S/ITS Metagenomics

Microbial community profiling and identification using amplicon sequencing for environmental and clinical samples.

Targeted Sequencing

Focused sequencing of specific genomic regions for cancer research, mutation detection, and biomarker discovery.

Run-only Sequencing

Bring your pre-made libraries for sequencing on our Illumina platforms. Ideal for labs with in-house library preparation capabilities.

Bioinformatics Services

Expert bioinformatics analysis to transform raw sequencing data into actionable insights.

Variant Calling

Identification of SNPs, indels, and structural variants from sequencing data with high accuracy and reliability.

Genome Assembly

De novo and reference-guided genome assembly for novel organisms and complex genomic regions.

Gene Expression Analysis

Differential gene expression, pathway analysis, and functional annotation from RNA-seq data.

Transcriptome Assembly

Reconstruction of full-length transcripts and isoform discovery from RNA sequencing data.

Taxonomical Classification

Microbial identification and community composition analysis from metagenomic sequencing data.

Custom Analysis

Tailored bioinformatics pipelines and analysis workflows designed to meet your specific research objectives.

Co-working Laboratory Space

We offer co-working laboratory space and Research for Hire services, providing researchers access to our state-of-the-art facilities and equipment.

Whether you need access to advanced sequencing platforms, laboratory bench space, or technical support, our co-working model makes cutting-edge research accessible to independent researchers, academic institutions, and startup biotech companies.

State-of-the-Art Facilities Research for Hire Technical Support