What the work is
Analyze chromosomes or chromosome segments found in biological specimens, such as amniotic fluids, bone marrow, solid tumors, and blood to aid in the study, diagnosis, classification, or treatment of inherited or acquired genetic diseases. Conduct analyses through classical cytogenetic, fluorescent in situ hybridization (FISH) or array comparative genome hybridization (aCGH) techniques.
On a typical day
- Develop and implement training programs for trainees, medical students, resident physicians or post-doctoral fellows.
- Stain slides to make chromosomes visible for microscopy.
- Summarize test results and report to appropriate authorities.
- Select or prepare specimens and media for cell cultures using aseptic techniques, knowledge of medium components, or cell nutritional requirements.
- Select banding methods to permit identification of chromosome pairs.
- Identify appropriate methods of specimen collection, preservation, or transport.