Whole Genome Sequencing (100 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 (100 Gb data) provides ultra high throughput data for the most demanding genomic investigations. This service facilitates large scale sequencing and high resolution genomics via genome sequencing for molecular diagnostic research testing and deep variant analysis.