At GenomeX, our WES process includes a comprehensive suite of services, starting with sample collection and preparation using advanced kits to ensure DNA integrity and optimal yield. We perform high-throughput sequencing on state-of-the-art platforms, achieving over 99% exome coverage with superior depth. Our bioinformatics analysis identifies single nucleotide polymorphisms (SNPs), insertions and deletions (indels), and copy number variations (CNVs), followed by functional annotation and prioritization of genetic variants. The results are presented in detailed, easy-to-understand reports, and significant findings are validated using gold-standard techniques.