Most neoplastic diseases have chromosome abnormalities. Cytogenetic studies are useful in diagnosis, treatment and prognosis of neoplastic diseases. Characteristic cytogenetic abnormalities are recognized as significant elements for disease classification in the 2008 WHO classification of hematological Malignancies. Specific chromosome abnormalities correlate with particular tumors subtypes. Cytogenetic testing is also useful in monitoring engraftment status and minimal residual disease after bone marrow or hematopoietic stem cell transplantation. Standard karyotype analysis in conjunction with Fluorescence in Situ Hybridization (FISH) is an important and integral component in the diagnosis and management of solid tumors. AGILE provides a comprehensive test menu for diagnosis and evaluation of hematologic malignancies and solid tumors.
Chromosome abnormalities are dectected by cytogenetic testing which include standard karyotype analysis and/or Fluorescence In Situ Hybridization (FISH). Karyotype analysis examines the number and the structure of the chromosomes in the cells.
Individual FISH tests are available for disease specific translocations or gene rearrangements, common numerical and structural abnormalities in specific neoplastic diseases, disease specific gene/locus deletion and amplifications, monitoring engraftment status and minimal residual disease after transplantation.
Maternal / Prenatal Screening
Pre-eclampsia Screening and Diagnosis
Non Invasive Prenatal Screening (NIPS)