Human Whole Genome Sequencing
Our human whole genome sequencing (WGS) service can be applied to a wide range of human genetics research applications, including cancer and disease-associated mutations study, genetic variations and pathogenic gene analysis, as well as precision medicine research.
We provide high quality, cost-efficient WGS services in a range of coverages to suit all research requirements.
We provide high quality, cost-efficient WGS services in a range of coverages to suit all research requirements.
Features and Advantages
Guaranteed data quality at competitive pricing
Fast local data delivery in the United States
Experienced pre-sales and after-sales support
Services in a range of coverages and read length to suit all research requirements
Sequencing Standards
PE100 or PE150
Guaranteed 80% of bases with quality score of Q30
- Standard sequencing coverage 30X/90Gb data (60X is recommended for cancer samples)
Sampling Requirements
Regular Samples
PCR Library
≥ 200 ng (Recommend ≥ 400 ng)
≥ 8 ng/μL
PCR-free Library
≥ 1 μg (Recommend ≥ 2 μg)
≥ 12.5 ng/μL
Low Input Samples:
≥ 50 ng
≥ 2.5 ng/μL
Service Details
Typical 10 working days from sample QC acceptance to data delivery
Expedited services are available, contact your local representative for details
- Reports and output data files are delivered in standard file formats: BAM, .xls, .png and FASTQ data
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