We believe you have a First Amendment right to information encoded in your genome – including your risk of developing common medical conditions and your likely response to drugs. However, the information provided in our non-clinical genome analysis is intended only for informational and educational purposes and research use, and should not be used for medical diagnosis, prognosis or treatment. Here’s how it works:
Standard 50X service
Silver = Standard + BAYSIC™ calls
Gold = Silver + VarIANT™ interpretation & analysis
100X CLIA Exome +
200X CLIA Exome +
We provide sequencing, variant detection and annotation, a genomic health report, and an interpretation of variant health implications – useful in a variety of clinical applications, including Oncology and Genetic Testing. Here’s how it works:
100X CLIA Lab
200X CLIA Lab
Tumor - Normal Pairs
30X-50X whole exome sequencing and standard analysis is competitively priced at $999 per sample. We can also provide deeper coverage, up to 200X whole genome coverage, and prices will scale accordingly.
We perform quick, accurate genome annotation and interpretation as well. We will provide a BAYSIC integrated variant call set (using at least Samtools, FreeBayes, and Atlas2 calls as input to BAYSIC) and BAYSIC vcf annotation for $99 per sample.
We will provide an interpretative exome analysis in light of relevant phenotypes, along with access to our VarIANT analysis tool, starting at $599 per sample.
Single Sample pricing below. For large projects involving multiple samples, please contact us for a quote
Standard Service $999 per Exome
Silver: Standard service plus BAYSIC Variant Calls $1099 per Exome.
Gold: Silver plus VarIANT interpretation and Analysis tool $1699
For further information about genome or exome sequencing and analysis, please contact us at or call 512.565.4693.