List of examinations offered
Accredited examinations
SP-CG-01 | Cytogenetic determination of caryotype from human cells | |
SP-CG-02 | Examination of biological material by FISH method | |
SP-MG-01 | Molecular genetic examination of gene mutations by PCR-RFLP method | |
SP-MG-02 | Molecular genetic examination of microdeletions in Y chromosome azoospermia factor region (AZFa, AZFb, AZFc) by multiplex PCR method | |
SP-MG-03 | Molecular genetic examination of gene mutations by reverse hybridization method | |
SP-MG-04 | Molecular genetic examination of 13, 18, 21, X, Y chromosome aneuploidies using STR markers by QF PCR method (Amnio PCR) | |
SP-MG-06 | Molecular genetic examination of gene mutations by Real-Time PCR method | |
SP-MG-08 | Mutation analysis/gene screening by Sanger sequencing method | |
SP-MG-09 | Gene mutation analysis by massive parallel sequencing method (MiSeq platform, Illumina) * | |
SP-MG-10 | Molecular genetic examination of fragile X chromosome syndrome (FRAXA) by PCR and TP-PCR method | |
SP-MG-11 | Examination of intragenic alterations by MLPA method (Multiplex Ligation - Dependent Probe Amplification) | |
SP-MG-12 | Examination of human genome alterations by Array CGH method | |
SP-MG-13 | Non-Invasive Prenatal Testing (NIPT) by massive parallel sequencing method (Illumina) | |
SP-MG-14 | Molecular genetic examination of HLA alleles associated with coeliac disease/gluten intolerance by SSP-PCR method |
*ONKO: ATM, BRCA1, BRCA2, BRIP1, CDH1, CHEK2, NBN, PALB2, PTEN, RAD51C, STK11, TP53, APC, CDH1, EPCAM, MLH1, MSH2, MSH6, MUTYH, BARD1, FAM175A, RAD50, RAD51D, PMS2/PMS2CL.
ONKO Plus: ATM, BRCA1, BRCA2, BRIP1, CDH1, CHEK2, NBN, PALB2, PTEN, RAD51C, STK11, TP53, APC, EPCAM, MLH1, MSH2, MSH6, MUTYH, BARD1, FAM175A, RAD50, RAD51D, PMS2, PMS2CL, MRE11A, PIK3CA, XRCC2
Non-accredited examinations
SP-CG-03 | Examination of biological material by FISH-PGD method |
SP-CG-05 | Determination of indicative spermiogram |
SP-MG-15 | Examination of human embryo genome alterations by Array CGH method |