Whole-genome, Exome and Targeted sequencing Analysis

variantFigure shows the substitution of 4.5kb portion of mm9 genomic reference with a transgene.

Whole-Genome Sequencing (WGS) is a process that determines the complete DNA sequence of an organism’s genome. This type of sequencing is mainly used in projects aimed at detecting the presence of SNPs, Indels and structural variants in a sample.

Exome sequencing is a technique to selectively sequence the coding regions of the genome as an effective alternative to whole-genome sequencing. This type of sequencing is most commonly used in projects aimed at detecting variants related to disease-causing protein structural and functional changes.

With targeted resequencing, a subset of genes or regions of interest are isolated and sequenced in high resolution. Pre-defined or customised gene panels enable researchers to focus on specific areas of interest, saving time and sequencing costs.

The following files can be provided with whole-genome, exome or targeted sequencing projects:

Bespoke downstream DNA sequencing analyses*:

* Please note that bespoke analyses might be subject to availability and resources, please contact us for more information.