Whole Genome Sequencing (25 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 (25 Gb data) generates the high data volume required for resolving repetitive elements in large genomes. This genome sequencing facilitates high resolution genomics and structural variation profiling for molecular biology research testing.