Whole Genome Sequencing (20 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 (20 Gb data) delivers a massive dataset for the detailed study of large genomes. It supports comparative genomics and population genetic analysis during genome sequencing for molecular biology research screening and large scale evolutionary mapping.