Mutations detection
According to your project, we propose low throughput services (primer design, PCR and sequencing) and high throughput solutions with enrichment, sequence capture and next generation sequencing using Roche® and Illumina® technologies.
We propose a pipeline of analyses dedicated to mutations identification and selection of SNPs of interest. For confirmation and biological validation of identified SNPs, we propose a complementary analysis on ABI ® 3730XL capillary sequencer.
