Genome Sequencing

This service covers viral, bacterial and small fungal genome sequencing that can be performed on the Illumina MiSeq instrument. This can either be de novo genome sequencing where there is no reference genome available or re-sequencing where a reference genome is available.

In cases where a reference genome is available, customers performing epidemiological studies etc can sequence bacterial genomes to low coverages. This type of data is useful for detection of SNPs & Indels in comparative studies.

This service covers genomes where a reference is available and customers are interested in comparative analysis including SNPs, Indels, structural variation (SV), copy number variation (CNV) etc. Here the genome is sequenced to a comparatively low coverage. We provide de novo whole genome sequencing services for all large genomes

We provide de novo whole genome sequencing services for all large genomes. This service is normally for customers with a genome that has not been sequenced before.