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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