Cytogenetic laboratory management : chromosomal, FISH, and microarray-based best practices and procedures
Cytogenetics In situ hybridization
John Wiley & Sons Incorporated
2017
EISBN 9781119069768
Guidelines for good clinical laboratory practice.
Quality management.
Design control of tests and FDA guidelines for laboratory developed tests (LDTs).
Pre-clinical validation studies.
Reagents, instruments and equipment.
Cost of testing and staffing requirements.
Process improvement : six sigma approach to laboratory improvement.
Staff training and competency for a cytogenetics laboratory.
Training program for cytogenetic and FISH technologists.
Training program for molecular genetic technologists.
General SOP information by test and pre-analytic procedures.
Analytic procedures : chromosome analysis.
Analytic procedures : FISH analysis.
Analytic procedures : microarrays.
Post-analytic procedures.
"This title will provide cytogenetic, FISH and microarray laboratory standard operating procedures (SOP's) and information on how to effectively write SOP's; validation plans and summaries; chemical, safety, quality control and quality assurance programs; and plans for effective use of reagents, instruments and equipment"--Provided by publisher.
Quality management.
Design control of tests and FDA guidelines for laboratory developed tests (LDTs).
Pre-clinical validation studies.
Reagents, instruments and equipment.
Cost of testing and staffing requirements.
Process improvement : six sigma approach to laboratory improvement.
Staff training and competency for a cytogenetics laboratory.
Training program for cytogenetic and FISH technologists.
Training program for molecular genetic technologists.
General SOP information by test and pre-analytic procedures.
Analytic procedures : chromosome analysis.
Analytic procedures : FISH analysis.
Analytic procedures : microarrays.
Post-analytic procedures.
"This title will provide cytogenetic, FISH and microarray laboratory standard operating procedures (SOP's) and information on how to effectively write SOP's; validation plans and summaries; chemical, safety, quality control and quality assurance programs; and plans for effective use of reagents, instruments and equipment"--Provided by publisher.
