Whole Genome Sequencing (35 Gb data)

• Isolation of NGS quality gDNA (if required) with QC.
• Fragmentation (if required) with QC.
• Preparation of appropriate library for sequencing on Illumina platform with QC.
• Sequencing using relevant PE read chemistry to generate committed data.
• Sequencing Run information.
• Raw data information (number of quality reads generated including average Q score), adaptor trimmed and clipped reads as fastQ files.
Whole Genome Sequencing (35 Gb data) provides extensive genetic data for the comprehensive analysis of large eukaryotic genomes. This genome sequencing service facilitates deep coverage mapping and high throughput genomics for molecular biology research testing and the identification of complex structural variants.