Re-sequencing of genomic fragments is the sequencing of presequenced and preselected genomic regions such as exons in order to find a correlation between sequence deviations (e.g. SNPs or indel mutations) and phenotypes. Based on Sanger technology,this service is performed in three phases
Phase I: Establishment of the PCR
Phase II: PCR and Sequencing
Phase III: Bioinformatics Analysis Identification of all differences between reference and samples
