Exome sequencing allows you to analyze the coding regions and UTR sequences of samples of your cohorts to identify common or rare changes : SNPs, mutations and indels within your association studies, epidemiological studies , clinical trials, pharmacogenetics and pharmacogenomics.
With its expertise in the field of human genetics, our team will provide you with a quality service by combining TruSeq capture technologies (Illumina) or V4/V4 + UTR SureSelect (Agilent) with HiSeq2000 technology (Illumina). Our offer includes the analysis of your datas using a standardized bioinformatics pipeline developed in-house. This pipeline allows you to receive a list of common or rare events identified in the samples.
Your interest concerns other than human exome? Contact us.
Our team of bioinformaticians can help you in analyzing your datas. Find our solutions in bioinformatics
Do not esitate to contact us for an appropriate training. Find our training solutions.