SOPHiA Hereditary Cancer Community Panels

Detection of SNV, InDel and CNV germline mutations in 35-144 genes using NGS.

More detailed product information

NGS panels for the detection of germline mutations (SNVs, indels and CNVs) in 35-144 genes associated with breast, ovarian, prostate, kidney,
stomach, melanoma, Lynch and intestinal polyposis syndrome.
Library preparation is based on hybridization capture technology.

The kit is validated for Illumina NGS sequencers.

The solution also includes the unique SOPHiA DDM software for secondary and tertiary analysis of the resulting NGS data.

CS2141ILLRGLY01	SOPHiA Custom Hereditary Cancer Solution - 35 genes	35 genes
CS2357ILLRGLY01	SOPHiA Custom Hereditary Cancer Solution - 59 genes	59 genes
CS2435ILLRGLY01	SOPHiA Custom Hereditary Cancer Solution - 66 genes	66 genes
BS0123ILLRGLY10	SOPHiA DDM™ HCS v2.0	83 genes
CS2453ILLRGLY01	SOPHiA Custom Hereditary Cancer Solution - 117 genes	117 genes
CS2225ILLRGLY01	SOPHiA Custom Hereditary Cancer Solution - 144 genes	144 genes

For more information, please contact us by e-mail: diagnostika@pentagen.cz