Whole Genome Sequencing (60 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 (60 Gb data) offers the data density necessary for resolving repetitive sequences and complex rearrangements in the genome. It facilitates genomic architecture analysis and exhaustive genomic mapping via genome sequencing for molecular biology research screening.