SNP Genotyping is rapidly becoming an indispensable tool for the analysis of many common diseases.
Precision Biomarker Resources has the capacity and the expertise to enable your research with this powerful technique.
Whether you want to analyze hundreds or even thousands of samples to discover new genetic associations in a population-based
study or you only want to look at tens of samples to determine LOH in clinical samples, Precision’s SNP Genotyping service
will provide you with access to the right tools, the throughput capacity and the high-quality data your research demands.
The Capacity to Handle Your Population-Based Studies
As genetic association studies become larger, sample numbers can reach the hundreds to thousands
in a single study. This can easily overwhelm a core lab that is not equipped for projects of this size, leading to
unwelcome delays. Precision Biomarker Resources high-throughput processing enables your research to proceed uninterrupted
and without straining your resources.
Cost-Effective Data Acquisition
With more than 906,600 SNPs and an additional 946,000 copy number probes, the Affymetrix
SNP Array 6.0 offers unparalleled coverage of the human genome. Put the strength of this array to work in your lab by
having Precision Biomarker Resources process your samples for less than a tenth of a penny per SNP.
Consistent Quality
It takes time to collect samples and gather the patient histories and phenotypic correlates.
Many times the donors are no longer available and whatever sample material you have is all you will ever get. These
samples are not just valuable, they are irreplaceable.
As one of the first service-providers to offer processing of samples on the Affymetrix SNP Array
5.0 and 6.0 arrays, Precision Biomarker Resources is as experienced a lab as you will find. With SNP call rates that
consistently exceed Affymetrix's acceptance criteria, Precision Biomarker Resources provides you with the confidence that
your samples will produce quality data that you can use to further your research.
Basic bioinformatics including SNP call rate and percent heterozygosity plus a full quality control
report including post-hybridization global chip QC report is included with each experiment.
