Targeted sequencing either through a panel of primers for up to a target size of 0.5 Mb (1,560 amplicons) or through enrichment for larger target sizes. Here, customers can either define the content for custom designs or choose content from off-the-shelf Illumina compatible panels.
Targeted sequencing technology offers the ability to process a higher number of samples with higher depth coverage in order to detect the rarest of variants.
Whole Exome Sequencing
These panels target the entire exome. There are number of kits from a number of different suppliers that can be used here. The selection of kits is influenced by the content flanking the exonic regions that customers are interested in, such as UTRs etc.
Agiomix Labs – The Region’s Preferred Partner for Whole Exome Sequencing (WES)
Identification of common single-nucleotide variants (SNV’s)
Detection of Small insertion/deletion variants (INDELs)
Guaranteed high quality data read-out of samples
Quickest Turn Around Time (TAT)
Optional Annotations and Clinical reports
Alternative coverage levels of 50X – 150X
25% higher data output than supplier specifications
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At Agiomix, our lab uses standardized SOPs with QC gates after every stage in the workflow to ensure the integrity of the final result.