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.

Informed Genomics mission

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.

biopsy sequencing
custom design panel

Custom design your own panel

Individual projects may have unique requirements for the specific regions of the genome being targeted. Working with our sister company, Nonacus, we can help you design your own custom panel with which to complete the project.

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Complete design flexibility with Cell3™ Target panels from our sister company Nonacus.
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Personal and bespoke service to ensure aims of the project are met.
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Manufacture time < 4 weeks including NGS validation.

If you would like to collaborate with us on your own design, please complete our service request form and we’ll be in touch.

Informed Genomics service features

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Sample: We accept blood, plasma, saliva, FFPE curls, FF tissue, and extracted DNA samples.
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Capture method: Nonacus, Cell3™ Target enrichment.
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Sequencing Platform: Illumina, NovaSeq 6000.
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Sequencing Read Type: Paired-end 150 bp.
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Turnaround Time: 2~3 weeks (from sample receipt to FASTQ), rapid services available please enquire.
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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.

Request a service quote

DNA extraction required

Birmingham Research Park, 97 Vincent Drive, Birmingham