A variety of NGS services are offered by our experienced staff, ranging from any parts of NGS workflows to complete sample-to-answer solutions. These include library preparation, library quantification and quality control, sequencing, and data analysis. Typical sequencing applications performed at the core include whole-genome sequencing, whole-exome sequencing, RNA-seq, ChIP-seq, and amplicon sequencing. We accept libraries pre-made by users and support customized sample preparation and sequencing applications.
Please contact us for a free consultation. We look forward to working with you on your sequencing projects.