Single point of contact for any type of NGS data analysis
Your biological question must drive your NGS data strategy.
Whole Exome Sequencing (WES): give access to all the coding part of the genome at reduced cost. WES provides a large overview of coding variations and their phenotypes consequences.
Whole Genome Sequencing (WGS): gives access to the exhaustive genetic information. WGS sequencing includes both coding and none coding regions which also plays a crucial role in regulative regions.
Targeted Sequencing: explores any specific target in the genome at lower cost.
RNA Sequencing: gives access to transcriptomic information such as differential expression.
We have the recall expertise to advise you on the alternative best suited to your project.