Next Generation Sequencing Services
Targeted resequencing is a cost-effective method for investigating areas of interest with next generation sequencing. By focusing on regions that are most likely to be involved in the phenotype under study, it allows researchers to conserve resources, handle more manageable data sets and affordably deliver much higher coverage levels, allowing identification of rare variants.
We can provide sequencing services for individual projects or ongoing sample processing including sample reception and extraction, library preparation and capture and data delivery. Data analysis packages can also be offered.
Whole Exome Sequencing
Targeting all the protein coding regions in the human genome, WES offers the most comprehensive tool for detecting the genetic variations underlying cancers, Mendelian diseases and complex human disorders (and a more cost-effective approach than whole genome sequencing).
Tumour/Liquid Biopsy Sequencing
Targeted sequencing panels that detect genes and mutations specific to known cancer phenotypes in gDNA, FFPE or ctDNA samples.
A panel of 524 oncogenes for profiling and stratification of common cancers and response prediction to immunotherapy.
Custom design your own panel
Individual projects may have unique requirements for the specific regions of the genome being targeted. We can help you design your own custom panel with which to complete the project.
Complete design flexibility with Cell3™ Target panels.
Manufacture time < 4 weeks including NGS validation.
Informed Genomics service features
Sequencing Platform: Illumina
Data transfer: We provide data releasing through SFTP download link or by loading into our partnered software companies’ software for data analysis and interpretation. Please enquire about bespoke bioinformatics solutions.