UW Heme Amplicon panel is a multiplexed gene panel assay that detects mutations related to treatment, prognosis, or diagnosis in the setting of hematolgical malignancy. The regions of the genes included in the panel are amplified using amplification technology and sequenced on an Illumina instrument to detect single nucleotide variants, insertions, and deletions. This test is designed to detect somatic mutations in the setting of neoplasia, and is not designed to detect germline (heritable) mutations.
Code | Name |
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HOTSD | Heme Gene Panel Spec. Desc. |
HOTRES | Heme Gene Panel Result |
HOTINT | Heme Gene Panel Interpretation |
HOTG | Heme Panel Genes Analyzed |
HOTM | Heme Gene Panel Method |
Amplification of the stated genetic regions followed by sequencing using an Illumina instrument
Blood: 6 mL blood in LAVENDER top (EDTA) tubeBone Marrow: 1-2 mL in a LAVENDER top (EDTA) tube
Samples should be refrigerated and delivered to the Laboratory without delay.
Extracted DNA will be accepted only from CLIA certified laboratories.
Optimal results are achieved when samples are received within: 72 hours of collection for bone marrow and peripheral blood
Samples submitted outside of these ranges will be evaluated for quality using appropriate internal controls and the results qualified appropriately.
Other |
Hematopathology, Molecular
206-606-7060 UW Hematopathology Laboratory, G7-800 |
Hematopathology, Molecular hours: |
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