Whole Genome Sequencing (8 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 (8 Gb data) offers balanced coverage for quantifying genetic variations across a target organism. It facilitates functional genomics and mutation frequency detection via genome sequencing for molecular diagnostic research testing and trait analysis.