CFCM Academy / Curriculum edition

Understand the signal.
Strengthen the interpretation.

A structured learning framework for clinical flow cytometry, from instrument physics and laboratory quality to disease-specific analysis.

Explore seven modulesBrowse by disease

Explore all 95 topics

Find a topic by keyword, module or disease and open its curriculum outline.

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The curriculum is open to explore

Explore module outlines and learning pathways, then work through the first seven editorially approved lessons below. Each lesson includes a worked example, questions and source references. More lessons and cases are in development.

Our publishing sequence is simple: learn → verify → synthesise → publish. Each teaching item needs traceable sources and accountable editorial review before release. Independent scientific review will be identified only where it has actually occurred.

Seven modules. One connected practice.

Start with the foundations or enter through a practical question. MRD is studied within each relevant disease pathway.

Module 01

Understanding the Physics of Flow Cytometry

Explore the instrument from sample stream to measured signal, with a learning sequence covering light, fluorescence and measurement quality.

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Module 02

Cytometry Laboratory GMP & Quality

Follow the laboratory workflow through quality control, documentation and traceability. Topics distinguish general quality practice from requirements that depend on the laboratory's intended activities.

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Module 03

Panel Design Insights

Build a structured approach to selecting markers and fluorochromes, then review controls and the evidence needed to assess a panel.

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Module 04

Cytometer & Panel Setup

Connect instrument setup with panel optimisation and long-term monitoring. The curriculum separates transferable principles from instrument-specific instructions.

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Module 05

Troubleshooting & Problem Solving

Work through problems by identifying the affected stage, checking evidence and documenting the investigation before changing a workflow.

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Module 06

Validation & Verification

Organise a study around intended use, performance claims and the questions that its data must answer. The topics connect study design, analysis and reporting.

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Module 07

Data Analysis of Haematological Malignancies

Learn through disease-centred pathways that connect diagnostic interpretation, follow-up and case discussion. MRD is studied within the relevant disease pathway.

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Within data analysis

Find your disease pathway

Diagnostic interpretation, follow-up and MRD are organised in their clinical context.

Disease pathway

B-cell Acute Lymphoblastic Leukaemia (B-ALL)

A disease-centred learning pathway for B-cell Acute Lymphoblastic Leukaemia (B-ALL). Explore diagnostic interpretation, follow-up, reporting and case discussion within the same clinical context.

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Disease pathway

T-cell Acute Lymphoblastic Leukaemia (T-ALL)

A disease-centred learning pathway for T-cell Acute Lymphoblastic Leukaemia (T-ALL). Explore diagnostic interpretation, follow-up, reporting and case discussion within the same clinical context.

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Disease pathway

Acute Myeloid Leukaemia (AML)

A disease-centred learning pathway for Acute Myeloid Leukaemia (AML). Explore diagnostic interpretation, follow-up, reporting and case discussion within the same clinical context.

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Disease pathway

Chronic Lymphocytic Leukaemia (CLL)

A disease-centred learning pathway for Chronic Lymphocytic Leukaemia (CLL). Explore diagnostic interpretation, follow-up, reporting and case discussion within the same clinical context.

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Disease pathway

B-cell lymphoproliferative disorders (B-LPD)

A disease-centred learning pathway for B-cell lymphoproliferative disorders (B-LPD). Explore diagnostic interpretation, follow-up, reporting and case discussion within the same clinical context.

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Disease pathway

Plasma cell neoplasms

A disease-centred learning pathway for Plasma cell neoplasms. Explore diagnostic interpretation, follow-up, reporting and case discussion within the same clinical context.

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Disease pathway

Myelodysplastic neoplasms / MDS

A disease-centred learning pathway for Myelodysplastic neoplasms / MDS. Explore diagnostic interpretation, follow-up, reporting and case discussion within the same clinical context.

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Choose a learning path

Suggested learning sequences connect the curriculum. The first seven lessons are available below; progress tracking is not active.

Latest released learning

Lessons, cases and resources appear only after their stated editorial checks are complete. Independent scientific review is identified separately when it has actually occurred.

Lesson

Use time to investigate an acquisition anomaly

Investigate a transient event-rate change without automatically deleting inconvenient events or mistaking event order for measured time.

Open learning item →

Lesson

Titration and detector setup: change one question at a time

Plan an interpretable antibody titration without confusing reagent amount, cell number, detector settings and the performance of the full panel.

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Lesson

A brighter plot is not necessarily a better measurement

Use a simple measurement model to distinguish collected signal, electronic scaling and display choices. Learn why larger numbers alone do not prove better resolution.

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Lesson

Green beads, uncertain assay: reading QC in context

Use a synthetic change investigation to understand the boundary between an instrument QC pass and evidence that the complete assay remains fit for use.

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Lesson

Compensation, spreading and FMO: three different questions

Distinguish correction of fluorescence spillover from the uncertainty that remains, then use an FMO control without overclaiming what it proves.

Open learning item →

Lesson

Rare events: a count, a denominator and a defensible claim

Calculate a rare-event fraction and its idealised counting uncertainty without confusing either with validated detection, quantification or a clinical MRD conclusion.

Open learning item →

Lesson

A perfect correlation can still fail a method comparison

Use a deliberately simple comparison to distinguish correlation, bias and fitness for an intended use. Includes a worked example and a review checklist.

Open learning item →

Cases & challenges

Released cases will connect observations, interpretation, differential diagnoses and the limits of the evidence. Questions will appear before the explanation.

No Academy cases have been released yet. Patient-identifiable material will not be used.

Read existing Clinical Notes →

Learning levels

Foundation → Intermediate

Build the concepts, then connect them to practical laboratory decisions.

Advanced → Expert case

Examine complex interpretation, validation decisions and uncertainty.

Search the curriculum or choose one of the released lessons. Lesson-level filters and progress tracking are not available.

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