Details on our NGS panels and single variant assays are available below:
JAK2, CALR, MPL, SF3B1, KIT, CSF3R, ETNK1, SH2B3, ASXL1, CBL, EZH2, IDH1, IDH2, KRAS, NRAS, RUNX1, SETBP1, SRSF2, TET2, TP53, U2AF1, ZRSR2.
$475 (non-MBS eligible)
$357 (MBS item 73398)
$612.10 (MBS item 73399)
Preferred samples: 4 ml peripheral blood (EDTA) OR 1-2 ml bone marrow (EDTA)
TAT: 21 days
Methodology: Next Generation Sequencing (NGS)
ABL1, ARAF, ASXL1, BAX, BCL2, BCOR, BCORL1, BIRC3, BRAF, BTK, CALR, CARD11, CBFB, CBL, CCND1, D274, CD79B, CEBPA, CSF3R, CXCR4, DDX3X, DDX41*, DNMT3A, EGR2, ETNK1, ETV6, EZH2, FLT3, FYN, GATA1, GATA2, ID3, IDH1, IDH2, IRF8, JAK1, JAK2, JAK3, KIT, KRAS, MAP2K1, MEN1, MPL, MYD88, NF1, NFKBIE, NOTCH1, NOTCH2, NPM1, NRAS, PDCD1LG2, PDGFRA, PIGA, PIK3CD, PLCG1, PLCG2, PPM1D, PTEN, PTPN11, RHOA, RRAGC, RUNX1, SETBP1, SF3B1, SH2B3, SMARCA2, SMARCA4, SRSF2, STAG2, STAT3, STAT5B, STAT6, TET2, TP53, U2AF1, UBA1, UBTF, WT1, XPO1, ZRSR2
*Excluded on request.
**FLT3-ITD included when requested
$829.10 (fully covered by MBS item no. 73447/73448)
Preferred samples:
4 ml peripheral blood (EDTA);
1-2 ml bone marrow (EDTA);
Tissue – fresh or FFPE block/slides (10 x 5 micron sections on positively charged slides)
TAT: 21 days
Methodology: Next Generation Sequencing (NGS)
ABL1, ABL2, AFDN, AFF1, ALK, BCL11B, BCR, BRAF, CBFA2T3, CBFB, CPSF6, CREBBP, CRLF2, CSF1R, DEK, ELL, EPOR, ERG, ETV6, FGFR1, FGFR3, FIP1L1, FLT3, FUS, GLIS2, HLF, IL2RB, JAK2, KAT6A, KMT2A, MECOM, MEF2D, MLF1, MLLT1, MLLT10, MLLT11, MLLT3, MNX1, MRTFA, MYB, MYC, MYH11, NPM1, NTRK1, NTRK2, NTRK3, NUP214, NUP98, NUTM1, PAX5, PBX1, PCM1, PDCD1LG2, PDGFRA, PDGFRB, PICALM, PML, PTK2B, RARA, RARG, RBM15, RET, RUNX1, RUNX1T1, TCF3, TSLP, TYK2, UBTF, USP2, ZMYM2, ZNF384
$700 (MBS eligible under DNA&RNA item no. 73445/73446)
Preferred samples:
20ml peripheral blood (EDTA);
1-2ml bone marrow (EDTA)
Tissue - fresh or FFPE block/slides (10 x 5 micron sections on positively charged slides)
TAT: 21 days
Methodology: Next Generation Sequencing (NGS)
$196.35 (non-MBS eligible)
Fully covered (MBS item 73314)
Preferred samples:
4 ml peripheral blood (EDTA) OR 1-2 ml bone marrow (EDTA)
TAT: 7 days
Methodology: Fragment analysis by capillary electrophoresis
$196.35 (non-MBS eligible)
Fully covered (MBS item 73314)
Preferred samples:
4 ml peripheral blood (EDTA) OR 1-2 ml bone marrow (EDTA)
TAT: 7 days
Methodology: Fragment analysis by capillary electrophoresis
$196.35 (non-MBS eligible)
Fully covered (MBS item 73314)
Preferred samples:
20 ml peripheral blood (EDTA) OR 1-2 ml bone marrow (EDTA).
Sample must be received within 72 hours of collection.
TAT: 7 days
Methodology: reverse transcription quantitative PCR (RT-qPCR)
Type A, B or D
$196.35 (non-MBS eligible)
Fully covered (MBS item 73314)
Preferred samples:
20 ml peripheral blood (EDTA) OR 1-2 ml bone marrow (EDTA).
Sample must be received within 72 hours of collection.
TAT: 14 days
Methodology: reverse transcription quantitative PCR (RT-qPCR)
$129 (not MBS covered)
Preferred samples:
4 ml (pre-transplant)/ 18 ml (post-transplant) peripheral blood (EDTA) OR
1-2 ml bone marrow (EDTA).
Post-transplant samples must be received within 72 hours of collection.
TAT: 14 days
Methodology: Short tandem repeat (STR) fragment analysis by capillary electrophoresis
$550 (not MBS covered)
Preferred samples:
4 ml peripheral blood (EDTA) OR 1-2 ml bone marrow (EDTA)
TAT: 28 days
$250 (not MBS covered)
Preferred samples:
4 ml peripheral blood (EDTA) OR 1-2 ml bone marrow (EDTA)
TAT: 28 days
Methodology: Sanger sequencing
Responses to commonly asked questions regarding testing for known or suspected haematological malignancies using NGS testing are outlined in our referrers guide.
Research program
As a proud member of the Collaborative Centre for Blood Cancer Genomics, the Wilson Centre leads a dynamic research program focused on targeted treatment resistance, personalised medicine, bone marrow failure syndromes, and residual disease. To learn more about our research program and other initiatives, including progress on the Genomic Advances and Testing Equity Within Australian HaematologY (GATEWAY) project please visit Wilson Centre for Blood Cancer Genomics.
Our Story
The Wilson Centre for Blood Cancer Genomics owes its formation to the remarkable generosity of the Wilson family. Their initial donation in 2017 paved the way for the Centre's establishment, with a subsequent contribution in 2021 further supporting its vision and activities. The Wilson family have now donated more than $9 million through the Snowdome Foundation to the Wilson Centre for Blood Cancer Genomics.
The team at the Wilson Centre for Blood Cancer Genomics is forever grateful to Bruce and Christine, and their children James, Andrew and Pennie and their families for their support.
How to contact us
For all testing and research enquiries to the Wilson Centre, please see the below contact details.
Contact the Wilson Centre team:
Phone: (03) 8559 5414
Fax: (03) 8559 5437
Email: This email address is being protected from spambots. You need JavaScript enabled to view it.
Request Form:
Molecular Haematology Request Form
Related pages
Go back to the Molecular Pathology page