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45-1 Ramsey Road, Shirley,
NY 11967, USA
Tel: 1-631-372-1052
Fax: 1-631-614-7828
Email:

Europe
Tel: 44-207-048-3343

Human Whole Genome Sequencing


human whole genome sequencing

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:
Data filtering
Alignment report
SNPs and indel calling
CNV detection and breakpoint determinations with single nucleotide precision
Determination of structural variations
Annotations and data mapping
Other customized analysis


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CONTACT CD GENOMICS
45-1 Ramsey Road, Shirley, NY 11967, USA
Tel: 1-631-372-1052
Fax: 1-631-614-7828
Email:

Europe
Tel: 44-207-048-3343

SERVICES
Sequencing
Microarray
Genotyping
Aptamers
Custom Libraries
Technology Platforms
Products

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