(RRID: SCR_027525)
AMDL is a clinical CAP/CLIA accredited molecular diagnostics laboratory at the Princess Margaret Cancer Centre, located on the 7th floor. The primary mission of AMDL is to support clinical trials and translational research projects requiring clinical-grade (CAP/CLIA) molecular testing at Princess Margaret Cancer Centre. AMDL works closely with our partner Molecular Diagnostics lab in Toronto General Hospital to transition protocols into clinical tests.
The AMDL laboratory is led by Dr. Harriet Feilotter, who is a CCMG certified Laboratory Director. Due to the required laboratory accreditations (CAP# 7175217/CLIA# 99D1106115), laboratory technical staff must be certified CMLTO licensed Molecular Technologists. In addition, our team is also comprised of annotation and informatics supporting staff. The annotation team consists of PhD researchers that translate pertinent clinical and scientific literature that identify diagnostic, prognostic and targeted cancer therapy indicators for genetic testing results for patients with cancer or those at risk for hereditary cancer. AMDL staff also work very closely with our Princess Margaret Cancer Centre collaborators (pathologists, medical and surgical oncologists, geneticists, scientists and other physicians) to ensure that project needs are met and clinical research and translational studies are performed to a high clinical standard.
Since 2011, over
samples have been processed
Trusted by over
researchers
Over
years of experience since 2011
In collaboration with the physicians at Princess Margaret Cancer Centre and the Cancer Genomics Program, the AMDL develops, evaluates, and implements high complexity genomic tests to meet the needs of clinical programs.
Don't see what you need? Please contact us.
AMDL helps support our clients by providing tailored services and study-specific requisitions. We offer a variety of services to support research activities, including nucleic acid extraction and banking, next-generation sequencing (Illumina and Ion Torrent platforms), NanoString, ddPCR, MLPA, and Sanger sequencing. Please see below for our current testing menu or contact us for more information.
Processing and extraction along with CAP/CLIA sample banking.
** Scroll to the right to see the whole table.
| Sample Type | Product | Extraction Method | Kit | Quantification Method | Available Testing |
|---|---|---|---|---|---|
| Blood/Plasma/BAL/Body Fluids | cfDNA (cell-free DNA) | Automated (King Fisher Apex) | MagMAX™ Cell-Free DNA Isolation Kit | 4150 TapeStation | NGS |
| cfTNA (cell-free DNA and RNA) | Automated (King Fisher Apex) | MagMAX™ Cell-Free Total Nucleic Acid Isolation Kit | 4150 TapeStation | ||
| Blood | Plasma | Manual | N/A | N/A | N/A |
| Blood, bone marrow, tissue (FFPE, fresh frozen), saliva, cell lines/pellets, buffy coats | DNA | Manual |
QIAGEN:
|
Qubit 2.0 |
ddPCR (various assays) NGS |
| Automated (Maxwell® RSC, QIAsymphony) |
Maxwell® RSC:
|
||||
| Blood, bone marrow, tissue (FFPE), cell lines/pellets | RNA | Manual | QIAGEN RNeasy Mini Kit |
Qubit 2.0 4200 TapeStation |
ddPCR (various assays) NGS NanoString - LSC17 |
| Automated (Maxwell® RSC) |
Maxwell® RSC:
|
||||
| Tissue | miRNA | Automated (Maxwell® RSC) | miRNA Tissue Kit (miRNA + total RNA) | TruSight Oncology 500 (Illumina) |
** Scroll to the right to see the whole table.
| Accepted Sample Type |
Extracted/Accepted Nucleic Acids |
Sample Requirements |
|---|---|---|
| Blood/Plasma (Streck) | DNA cfDNA |
ddPCR: 1 full streck tube (8-10ml) NGS: 2 full streck tubes (8-10ml each) |
| Blood/Bone Marrow | DNA RNA |
1 ml |
| FFPE Tissue | DNA RNA |
FFPE Tumour tissue with 25mm2 tumour tissue
surface area (minimum 10mm2) and with minimum
30% nucleated tumour cells
|
| Fresh Frozen Tissue (Laser-Capture Micro-dissected) | DNA |
>1M cells (total)
Sample(s) must arrive in fresh cell lysis solution prepared by the lab. Please contact us. |
| Saliva | DNA | Full Oragene collection tube (saliva to "Fill line" on OG-600 tube, mixed with stabilizers included in integrated lid) |
| Nucleic Acids | DNA cfDNA RNA |
Assay dependent - Please contact the laboratory to inquire |
| Cell suspensions/pellets, lines (or fixed cells/cell lines) | DNA |
Assay dependent - Please contact the laboratory to inquire |
| BAL/Body Fluids/CNB Supernatant | cfDNA DNA |
Assay dependent - Please contact the laboratory to inquire |
A comprehensive investigation of cancer genes and selected non-cancer genes within patient blood/plasma and tumour samples can provide information about diagnosis, patient risk stratification and response to therapy, as well as help determine potential application of targeted therapies for different malignancies.
** Expand the panels below or click the name of NGS Panels on the last column for more detailed information.
| Sample Type | Sample Source | NGS Panels |
|---|---|---|
| cfDNA (cell-free DNA) | Plasma | |
| DNA | Blood, bone marrow, tissue (FFPE, fresh frozen), saliva, cell lines/pellets (fixed or suspensions) | |
| RNA | Blood, bone marrow, tissue (FFPE), cell lines/pellets (fixed or suspensions) |
NanoString technology enables the direct detection of RNA, DNA or protein in a sample using patented molecular barcodes and a unique hybridization and detection platform.
Panels currently validated and available:
LSC17 assay:
Custom 17 gene panel for stratifying acute myeloid leukemia
(AML) patients for their level of relapse risk. Read more about
it
here.
Platform: NanoString nCounter
Available for Research use:
ddPCR enables the quantitation of nucleic acids in a sample using a miniaturized PCR procedure that is executed in a high-throughput manner.
Design advice for your clinical research assay and validation and testing according to CAP/CLIA guidelines
a list of select projects we participated in
Ontario-wide Cancer Targeted Nucleic Acid Evaluation (OCTANE) tumour profiling initiative led by Dr. Phil Bedard.
Gynecologic cancers molecular profiling initiatives led by Drs. Amit Oza and Stéphanie Lheureux.
Validating novel liquid biopsy platforms for ctDNA NGS in routine clinical use for patients with advanced lung cancer, ensuring complete genotyping and evaluating molecular resistance to targeted therapy.
Evaluating genomic markers of response, in tissue and plasma, to combination therapy of binimetinib (MEK) plus pembrolizumab (PD-L1) in patients with treatment-naïve advanced stage non-small cell lung cancer (NSCLC).
Assessment of genomic markers for response and resistance to MET inhibitors in a platform study, enabling treatment access for patients with advanced NSCLC and alterations in MET/ROS1.
Select a year to see a listing of articles published.
* AMDL-led publications are shown in bold.
Please contact the lab director to discuss your clinical research project and how we can help.
AMDL offers several different advanced technologies to provide interpretable results. Details about these technologies and custom panels can be found in the ‘Our Services’ section. Information about commercially available panels can also be found on vendors’ websites. Please contact us so we can discuss and assist you with meeting your research objectives.
Contact us
for more details.
The annotation team leverages an in-house variant knowledgebase and custom pipeline for managing reporting of variants from NGS testing. The team gathers and reviews evidence from curated variant and gene databases, human disease knowledge resources, and clinical and scientific literature. Variants are classified based on the available evidence of the variant's degree of clinical actionability for somatic variants (Li et al., J Mol Diagn. 2017) or pathogenicity for germline variants (Richards et al., Genet Med. 2015).
Please
contact us for more details.
Yes, we are open to arranging visits, please
contact us.
For publications resulting from our services, please acknowledge the Advanced Molecular Diagnostics Laboratory (amdl.uhnresearch.ca) in the Acknowledgements section of your manuscript. Acknowledgements are an important reflection of our contributions to your published work, and help strengthen our applications for grant funding. We appreciate your acknowledgements!
In general, it is sufficient to reference amdl.uhnresearch.ca and/or Advanced Molecular Diagnostics Laboratory for tracking and reporting purposes. It is not required that Individual team members be named unless they have made a direct scientific contribution to your work that warrants authorship or specific acknowledgement.
To support accurate tracking of core facility usage in publications, please include the following Research Resource Identifier (RRID):
* A Research Resource Identifier (RRID) is a unique citation code that enables transparent reporting and recognition of core facilities in published research.
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