Bone Marrow Failure NGS Panel
Use
The Bone Marrow Failure NGS Panel is designed to identify genetic mutations associated with bone marrow failure syndromes. It is useful for understanding the genetic basis of such conditions, offering insights into diagnosis and management. The test analyzes multiple relevant genes to provide comprehensive genomic profiling, aiding in the detection of hereditary and acquired genetic alterations associated with bone marrow failure.
Special Instructions
The test is performed by Fulgent Genetics. It is important to ensure that specimens are not in direct contact with ice packs during transportation. For clients in New York State, please make sure to provide the date and time of specimen collection.
Limitations
This test may not detect all genetic mutations associated with bone marrow failure syndromes. There may be genetic variants that the test does not include in its analysis. Additionally, variations in the quality of the specimen could impact the test's ability to detect certain mutations. Full interpretation requires correlation with clinical and other laboratory findings, and results should be interpreted by a qualified healthcare professional.
New York Approved
Methodology
NGS (Targeted)
Biomarkers
Result Turnaround Time
null-37 days
Related Documents
For more information, please review the documents below
Specimen
Whole Blood
Volume
4 mL
Minimum Volume
Not provided
Container
EDTA tubes
Storage Instructions
Use cold pack for transport, making sure cold pack is not in direct contact with specimen.