Shallow Whole Genome Sequencing (sWGS)
Shallow Whole Genome Sequencing provides a cost-effective method to capture genome-wide variation at lower coverage. This service is ideal for applications such as copy number variation (CNV) profiling, large-scale cohort studies, and exploratory research where high-depth sequencing is not required. Our pipeline ensures reliable data generation with flexible options tailored to your study design [PLACEHOLDER].
Whole Exome Sequencing (WES)
Whole Exome Sequencing focuses on the protein-coding regions of the genome, offering a comprehensive yet efficient approach to identify variants with potential functional impact. This service is well-suited for studies on rare diseases, cancer genomics, and genetic association research. We deliver high-quality, clinically relevant data with customizable analysis options to meet your project’s needs [PLACEHOLDER].
Contact our Research Technicians for more detailed information
Jacqueline Egthuijsen
