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OncoSeq® C

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OncoSeq® C

OncoSeq® offers a comprehensive range of molecular genetic analysis reports that help identify genetic variations that could be associated with cancer development. The OncoSeq® reports were designed by expert clinicians working with a team of genetics scientists and bioinformaticians to develop reports that are easy to understand and help physicians and patients determine the most suitable prevention, early detection and management strategies for patients. OncoSeq® offers optional pre and post testing genetic counseling services to help patients understand their options and reports. OncoSeq® reports are generated by accredited and approved partner laboratories around the world using validated laboratory protocols to ensure the highest quality reporting.

OncoSeq® C

Read of 12 Genes - BRCA1, BRCA2, BRIP1, CHEK2, ERBB2, APC, MLH1, MSH2, MSH6, MUTYH, PMS2, TP53

OncoSeq® S

Read of 25 Genes – APC, ATM, BARD1, BRCA1, BRCA2, BRIP1, CDH1, CHEK2, EPCAM, MLH1, MSH2, MSH6, PALB2, PTEN, MUTYH, NF1, NF2, PIK3CA, PMS2, PTCH1, RAD50, RAD51C, RAD51D, STK11, TP53

OncoSeq® X

Read of 50 Genes - ATM, APC, BARD1, BRCA1, BRCA2, BRIP1, CDH1, CHEK2, EPCAM, FAM175A, MLH1, MRE11A, MSH2, MSH6, MUTYH, NBN, PALB2, PIK3CA, PMS2, PMS2CL, PTEN, RAD50, RAD51C, RAD51D, STK11, TP53, XRCC2, NF1, SPRED1, MEN1, RET, SMARCB1, NF2, LZTR1C, TNNB1, KRAS, ERBB2, ALK, EGFR, RB1, CDKN2A, CDK4, FLCN, RUNX1, XPC, WRN, PTCH1, CDKN1C, SMAD4, HRAS

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