CD Genomics proprietary GenSeq™ Technology provides high quality Human Whole Genome Sequencing service which based on Illumina's HiSeq X Ten Sequencing System. We also provide bioinformatic analysis options from raw data to the full publication-ready reports
CD Genomics offers highly accurate, complete human whole genome sequencing service utilizing the Illumina HiSeq X Ten. With its unprecedented speed, throughput and exceptional data quality, the high sequencing cost is no longer the barrier to comprehensive application of human whole genome sequencing
High Coverage Whole Genome Sequencing (30X)
Widely considered the standard for whole genome sequencing, 30X mean coverage is used for a wide variety of studies for the discovery and identification of variants including singe nucleotide variants, structural variants, and copy number variants in coding and non-coding regions .
Deep Coverage Whole Genome Sequencing (60X)
Useful for studies where deeper coverage is required, this product provides 60X mean coverage to increase the percentage of the callable genome, improving sensitivity to detect rare variants, while providing statistical power to filter false-positive calls .
CD Genomics Whole Genome Resequencing Applications:
SNPs and indel calling
CNV detection and breakpoint determinations with single nucleotide precision
Determination of structural variations
Annotations and data mapping
Other customized analysis