Test Catalog
Reference catalog for physician requests
This catalog lists the tests and panels performed at our center by service area. Tables include only methods, samples and turnaround times documented by our laboratory; for cells marked "—" please consult our laboratory.
Test requests must use the Test Request and Sample Delivery Form and, where required, the Informed Consent Form. Sample collection rules are detailed in the Sample Collection Handbook.
NIPT — Non-Invasive Prenatal Screening
Details →| Test / Panel | Method | Sample | Turnaround |
|---|---|---|---|
| NIPT — MomGuard / Verifi / Veritas | cfDNA · Next-generation sequencing (NGS) | Maternal venous blood | 10–14 days |
Cytogenetics (Chromosome Analyses)
Details →| Test / Panel | Method | Sample | Turnaround |
|---|---|---|---|
| Chromosome analysis from peripheral blood | Cell culture + chromosome analysis | Peripheral blood | — |
| Chromosome analysis from bone marrow | Cell culture + chromosome analysis | Bone marrow | — |
| Skin/tissue culture and chromosome analysis | Cell culture + chromosome analysis | Tissue | — |
| Chromosome analysis from amniotic fluid | Cell culture + chromosome analysis | Amniotic fluid | — |
| CVS culture and chromosome analysis | Cell culture + chromosome analysis | CVS (chorionic villus) | — |
| Fetal blood culture and chromosome analysis | Cell culture + chromosome analysis | Fetal blood | — |
| Chromosome analysis from pregnancy termination material | Cell culture + chromosome analysis | Tissue | — |
Molecular Cytogenetics (FISH)
Details →| Test / Panel | Method | Sample | Turnaround |
|---|---|---|---|
| Microdeletion/microduplication FISH (22q11.2, PWS/AS, Williams etc.) | FISH | Blood / bone marrow / amniotic fluid / CVS / tissue | — |
| Translocation/inversion/deletion confirmation FISH | FISH | Blood / bone marrow / amniotic fluid / CVS / tissue | — |
| Hematological fusion FISH (BCR::ABL1 etc.) | FISH | Blood / bone marrow / amniotic fluid / CVS / tissue | — |
| Rapid aneuploidy assessment (13, 18, 21, X, Y) | FISH · QF-PCR | Blood / bone marrow / amniotic fluid / CVS / tissue | — |
Women's Health and Obstetrics
Details →| Test / Panel | Method | Sample | Turnaround |
|---|---|---|---|
| Early trisomy test (QF-PCR) | QF-PCR | Amniotic fluid | — |
| Y chromosome microdeletion | FISH / MLPA (deletion analysis) | Peripheral blood | — |
| Thrombophilia panel | NGS panel | Peripheral blood | — |
Oncology
Details →| Test / Panel | Method | Sample | Turnaround |
|---|---|---|---|
| ALK | Mutation analysis | — | — |
| BRCA1 / BRCA2 | Mutation analysis | — | — |
| BRAF V600E | Mutation analysis | — | — |
| EGFR | Sequencing analysis | — | — |
| KRAS / NRAS | Mutation analysis | — | — |
| TP53 | Sequencing analysis | — | — |
| RET | Mutation analysis | — | — |
| MSI | MSI | — | — |
| NTRK | NGS | — | — |
| ABL1 (Imatinib resistance) | Sequencing analysis | — | — |
CTC — Liquid Biopsy
Details →| Test / Panel | Method | Sample | Turnaround |
|---|---|---|---|
| CTC identification panel | Immunofluorescence (microfluidic) | Venous blood | ~2 weeks |
| CTC ER / PR / HER2 | Immunofluorescence | Venous blood | — |
| CTC PD-L1 | Immunofluorescence | Venous blood | — |
Hematology
Details →| Test / Panel | Method | Sample | Turnaround |
|---|---|---|---|
| Alfa Talasemi (HBA1, HBA2, HBZ) | MLPA (deletion analysis) | — | — |
| Beta Talasemi (HBB) | Sequencing analysis | — | — |
| Sickle Cell Anemia (HBB) | Sequencing analysis | — | — |
| Hemofili A (F8) / Hemofili B (F9) | Sequencing analysis | — | — |
| Faktör 9 Defekti (F9) | Sequencing analysis | — | — |
| Hiperhomosisteinemik Tromboz (CBS) | Sequencing analysis | — | — |
| Bombay / Para Bombay Fenotipi (FUT1) | Sequencing analysis | — | — |
| Diamond–Blackfan Anemisi Tip 1 (RPS19) | Sequencing analysis | — | — |
| Human Platelet Antijen (HPA1–HPA15) | Genotyping | — | — |
| t(9;22) BCR/ABL — Philadelphia | FISH | — | — |
| t(15;17) PML/RARA | FISH | — | — |
| t(8;21) ETO/AML1 | FISH | — | — |
| t(12;21) TEL/AML1 | FISH | — | — |
| t(14;18) IgH/BCL2 | FISH | — | — |
| t(11;14) IgH/CCND1 | FISH | — | — |
| inv(16) / t(16;16) CBFB/MYH11 | Real-Time PCR | — | — |
| Del(20q) | FISH | — | — |
| Kimerizm (ayrı cinsiyet) | FISH | — | — |
Endocrinology and Metabolism
Details →| Test / Panel | Method | Sample | Turnaround |
|---|---|---|---|
| MODY Mutation Panel 1–2 | NGS panel | — | — |
| MEN Sequencing analysis | Sequencing analysis | — | — |
| HBOC | NGS panel | — | — |
| Hotspot cancer mutation panel | NGS panel | — | — |
| Familial cancer syndromes panel | NGS panel | — | — |
| Primary immunodeficiency panel | NGS panel | — | — |
| Febrile diseases panel | NGS panel | — | — |
| FMF (MEFV) | Sequencing analysis | — | — |
| Hereditary colon cancer panel | NGS panel | — | — |
| Solid Tumor Panel | NGS | — | — |
Nephrology
Details →| Test / Panel | Method | Sample | Turnaround |
|---|---|---|---|
| Monogenic glomerular disease panel | NGS panel | — | — |
| Cystic interstitial and tumoral disease panel | NGS panel | — | — |
| Tubular disease panel | NGS panel | — | — |
Rare Diseases
Details →| Test / Panel | Method | Sample | Turnaround |
|---|---|---|---|
| WES — Whole Exome Sequencing | NGS (WES) | — | — |
| Nörofibromatozis 1 / 2 Mutation Panel | NGS panel | — | — |
| Distrofin Geni Mutation Panel | NGS panel | — | — |
| Kistik Fibrozis Mutation Panel | NGS panel | — | — |
| CFTR — Sequencing analysis | Sequencing analysis | — | — |
| Tuberoskleroz Mutation Panel | NGS panel | — | — |
| Lizozomal Depo Hastalıkları Mutation Panel | NGS panel | — | — |
| Noonan Sendromu Mutation Panel | NGS panel | — | — |
| Glikojen Depo Hastalığı Mutation Panel | NGS panel | — | — |
| Hipertrofik Kardiyomiyopati Mutation Panel | NGS panel | — | — |
| LQT Mutation Panel | NGS panel | — | — |
| Glikozilasyon Bozukluğu Mutation Panel | NGS panel | — | — |
| Kalıtsal İşitme Kaybı Mutation Panel | NGS panel | — | — |
| Periyodik Ateş Sendromları Mutation Panel | NGS panel | — | — |
| Bardet Biedl Mutation Panel | NGS panel | — | — |
| Limb Girdle Musküler Distrofi Mutation Panel | NGS panel | — | — |
| Spinoserebellar Ataksi Mutation Panel | NGS panel | — | — |
| Alport Sendromu Mutation Panel | NGS panel | — | — |
| Kallmann Sendromu Mutation Panel | NGS panel | — | — |
| Prematür Ovaryen Yetmezlik Mutation Panel | NGS panel | — | — |
| Kadın / Erkek İnfertilitesi Mutation Panel | NGS panel | — | — |
| Mitokondriyal DNA Mutation Panel | NGS panel | — | — |
| Frajil X — Fragman Analizi | Fragile X fragment analysis | — | — |
| Connexin — Sequencing analysis | Sequencing analysis | — | — |
Preimplantation Genetic Diagnosis (PGT)
Details →| Test / Panel | Method | Sample | Turnaround |
|---|---|---|---|
| PGT / PGS | NGS | Embryo biopsy | — |
Pharmacogenetics
Details →| Test / Panel | Method | Sample | Turnaround |
|---|---|---|---|
| Drug-gene (pharmacogenetic) panel | NGS panel | — | — |
Sports Genetics
Details →| Test / Panel | Method | Sample | Turnaround |
|---|---|---|---|
| Spor ve Fitness Paneli (36 genes) | NGS panel | — | — |
Nutrition Genetics
Details →| Test / Panel | Method | Sample | Turnaround |
|---|---|---|---|
| Nutrigenetics panel | NGS panel | — | — |
CAR-T Monitoring
Details →| Test / Panel | Method | Sample | Turnaround |
|---|---|---|---|
| CAR transgene persistence (qPCR) | qPCR | — | — |
| B-Hücre Aplazisi / B-cell aplasia follow-up | Flow cytometry | — | — |
| MRD (Minimal residual disease) | Flow cytometry / NGS | — | — |
International Biological Material Transfer
Details →| Test / Panel | Method | Sample | Turnaround |
|---|---|---|---|
| International sample transfer and coordination service | — | Blood / bone marrow / amniotic fluid / CVS / tissue | — |
Important notice: This catalog is for information only and contains no prices (Turkish health promotion regulation). For sample types and current working/report times marked "—", please contact our laboratory: +90 312 920 13 62. Test results must always be evaluated by the requesting physician together with clinical findings.