About EuroClonality
EuroClonality is a European scientifically independent foundation aiming to promote continuous innovation and standardization of laboratory diagnostics in hemato-oncology with a special emphasis on clonality testing and supporting quality control and education in laboratory diagnostics. EuroClonality developed and standardized novel multiplex PCR assays for detection of immunoglobulin (IG) and T-cell receptor (TR) gene rearrangements. These assays are now widely used for the diagnosis of lymphoproliferative disorders.
Read more about EuroClonalityAbout the EuroClonality-NGS Working Group
The EuroClonality-NGS Working Group is a working group of EuroClonality that aims to research and set standards in IG/TR NGS methodology and its applications in hemato-oncology, hematology and immunology.
Read more about the EuroClonality-NGS Working GroupDiagnostic innovations by EuroClonality
Since the start of the collaboration in 1996, the EuroClonality Consortium has developed, optimized, standardized and validated various new assays and related tools to improve diagnostic patient care.
Read more about the diagnostic innovations by EuroClonalityEuroClonality EQA Scheme
Together with the Biomedical Quality Assurance Research Unit of the KU Leuven, EuroClonality organizes an annual External Quality Assessment scheme. All laboratories working with the EuroClonality/BIOMED-2 multiplex PCR assays for detection of IG/TR gene rearrangements can join this EQA scheme to evaluate their performance.
Read more about the EuroClonality EQA SchemeEuroClonality Educational Workshops
Each year, the EuroClonality Educational Workshop “Clonality Assessment in Pathology” is organized in Nijmegen, The Netherlands. This workshop addresses questions on pitfalls in technique and interpretation of the results of the EuroClonality/BIOMED-2 multiplex PCR assays.
Read more about the EuroClonality Educational WorkshopsSupport and Protocols
EuroClonality and the EuroClonality-NGS Working Group also offer support to the diagnostic community via the Online Diagnostic Support Service for problematic cases in clonality testing with the EuroClonality/BIOMED-2 assays, a FAQ section on the use of these assays, and by providing protocols of IG/TR NGS methodology.
ESLHO, together with the independent scientific foundations EuroFlow, EuroClonality and EuroMRD, is an official EHA Specialized Working Group (SWG).
EuroClonality at the EA4HP 2024 in Dubrovnik
Thank you European Association for Haematopathology for providing EuroClonality with a booth at the EA4HP 2024 meeting in beautiful Dubrovnik! If you are attending the meeting, pass by for our NGS educational book, latest publications, and info about the EuroClonality EQA and future educational events.
We're hiring
ESLHO is looking for a new colleague for the position of Technician/Quality Officer, who will support the organization of our quality assessment programs and the achievement and maintenance of ISO 17043 accreditation. As we are looking for a candidate who also speaks Dutch, the job description is in that language. Applications for this position are no longer being accepted. The submission deadline was 23 September 2024.
Open ESLHO Symposium on November 7th in Lisbon
ESLHO organizes the 13th ESLHO Symposium on the 7th of November in Lisbon, Portugal. At the Convento do Beato, renowned speakers from all over Europe will share their knowledge on Multi-omics approaches for diagnosis and monitoring of hematological malignancies.
EuroClonality publishes Recommendations for Evaluation of B-Cell Clonality Analysis by Next-Generation Sequencing.
NGS-based clonality analysis is a powerful technique for the assessment of Ig clonality, but it has its specific pitfalls. EuroClonality developed a step-by-step approach to interpretation of NGS-amplicon–based assessment of clonality which will allow a reliable and reproducible interpretation of the results and will help to avoid overinterpretation. This is all published in a paper named: EuroClonality-NGS Recommendations for Evaluation of B-Cell Clonality Analysis by Next-Generation Sequencing: A Structured Approach with the DEPART Algorithm.