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SOPHiA Lymphoma Solution

Product code: BS0116ILLRSMY05
Producer: SOPHiA GENETICS
NGS panel for the detection of SNV and InDel somatic variants using hybrid capture technology.

More detailed product information

NGS panel for detection of somatic mutations (SNV, InDel) in 54 genes associated with B- and T-cell lymphomas.
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.

List of genes involved: ARID1A, B2M, BCL2, CCND3, CD58, CHD2, CDKN2A, CDKN2B, CIITA, CXCR4, EP300, FOXO1, GNA13, ID3, IRF4, KMT2A,
KMT2D, MAL, MEF2B, MYC, MYD88, NFKBIE, PAX5, PIM1, POT1, PRDM1, PTPN11, REL, SOCS1, TNFAIP3, TNFRSF14, TP53, ATM, BCL6, BIRC3, BRAF,
BTK, CARD11, CCND1, CD79A, CD79B, CREBBP, EZH2, FBXW7, KRAS, NOTCH1, NOTCH2, NRAS, PLCG2, PTEN, SF3B1, STAT6, TCF3, XPO1


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