Whole Genome Sequencing (30 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 (30 Gb data) provides exhaustive data for the complete analysis of complex eukaryotic DNA. It supports comprehensive genomic mapping and whole genome characterization for molecular diagnostic research screening and advanced trait discovery.