Claritas Genomics announces the Nephrotic Syndrome Region of Interest (NS-ROI)
Claritas Genomics has launched the Nephrotic Syndrome Region of Interest (NS-ROI). The NS-ROI sequences 42 genes relevant to Nephrotic Syndrome, an increase of 13 genes from the original Nephrotic Syndrome Panel, which is now discontinued.
The NS-ROI is built on the Claritas Clinical Exome platform, which allows expansion into any Claritas exome product, and allows rapid changes to the gene list as discoveries in the field occur. Additionally, clients can request raw data in the form of VCF and BAM files for further investigation into the patient’s exome. Gene list, technical information, and associated services are described here.