For studies needing the most comprehensive information about important samples, OICR can perform whole genome sequencing with as little as 50 nanograms of input DNA. We've supported both large resequencing studies and rapid turnaround projects where data for each sample needs to be returned to clinical researchers.
|Standard coverage (30X)||
||Standard coverage whole genomes are adequate for most applications where variations are readily identifiable, such as germline SNVs or tumour cell lines with little heterogeneity.|
|Deep coverage (>50X)||
||Deep coverage genomes provide a more detailed view of DNA when cellular heterogenity is high, or where complicated structural changes such as chromothripsis are expected.|
|Interested in any of these services? work with us|